This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zhao, X.
Right arrow Articles by Xu, J.-R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zhao, X.
Right arrow Articles by Xu, J.-R.

Next Article 

Eukaryotic Cell, October 2007, p. 1701-1714, Vol. 6, No. 10
1535-9778/07/$08.00+0     doi:10.1128/EC.00216-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

MINIREVIEW

Mitogen-Activated Protein Kinase Pathways and Fungal Pathogenesis{triangledown}

Xinhua Zhao, Rahim Mehrabi, and Jin-Rong Xu*

Department of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana 47907


arrow
INTRODUCTION
 
In eukaryotic cells, a family of serine/threonine protein kinases known as mitogen-activated protein (MAP) kinases (MAPKs) is involved in the transduction of a variety of extracellular signals and the regulation of different developmental processes. The MAPK is activated by dual phosphorylation of the TXY motif by MAPK kinase (MEK or MAPKK), which is activated in turn by MEK kinase (MEKK or MAPKKK). The sequential activation of the MAPK cascade eventually results in the activation of transcription factors and the expression of specific sets of genes in response to environmental stimuli. In the budding yeast Saccharomyces cerevisiae, five MAPK pathways are known to regulate mating, invasive growth, cell wall integrity, hyperosmoregulation, and ascospore formation (50). In the past decade, MAPKs in various plant and human pathogenic fungi have been characterized. In this review, we will compare their functions in different fungal pathogens with a focus on infection-related morphogenesis and virulence.


arrow
MAPK PATHWAYS IN S. CEREVISIAE
 
Because of advanced studies with S. cerevisiae, we will first present a brief overview of yeast MAPKs (Fig. 1). The pheromone response pathway (for reviews, see the work of Bardwell [9] and of Schwartz and Madhani [132]) is initiated by the binding of pheromone with a G-protein-coupled receptor (GPCR), Ste2 or Ste3, and the dissociation of an inhibitory G{alpha} subunit, Gpa1, from stimulatory Gß{gamma} subunits. The liberated Gß directly associates with a scaffold protein Ste5 and a p21-activated protein (PAK) kinase, Ste20, and is essential for the activation of the Ste11-Ste7-Fus3/Kss1 cascade. The cyclin-dependent kinase inhibitor Far1 and the Ste12 transcription factor are activated by Fus3 and Kss1 MAPKs for regulating the mating processes. Several elements of the pheromone response pathway are also involved in filamentous growth, which represents invasive growth in haploid and pseudohyphal development in diploid cells. The specificity of Fus3 and Kss1 cascades is regulated by Ste5, the Ste12/Tec1 transcription factor complex, and controlled degradation of Tec1 or Ste12 (12, 28, 132). For filamentous growth, the Kss1 pathway is activated by Ras2, Cdc42, 14-3-3 proteins Bmh1 and Bmh2, and Ste50 (9). The Ras2/cyclic AMP (cAMP) signaling also regulates filamentous growth via the GPCR Gpr1 and G{alpha} Gpa2 subunit (114).


Figure 1
View larger version (31K):
[in this window]
[in a new window]

  		FIG. 1. MAPK pathways in Saccharomyces cerevisiae.

The Pkc1-Slt2 (Mpk1) cell integrity pathway monitors cell wall integrity and promotes cell wall biosynthesis (for a review, see the work of Heinisch [52]). It is also involved in responses to certain environmental signals, including low osmolarity, high temperature, alkaline pH, and nutrient limitations. Extracellular signals are transmitted from surface sensors to Rom2, a guanine exchange factor of the GTP-binding protein Rho1. Rho1 then activates Pkc1 and the Bck1-Mkk1/Mkk2-Slt2 cascade (Fig. 1). Downstream transcription factors, such as Rlm1, Sbf, and Swi6, are activated by Slt2 to regulate cell wall synthesis and cell cycle (52, 60). The high-osmolarity glycerol (HOG) response pathway is required for growth under hyperosmotic conditions (54, 129). The Pbs2 MEK-Hog1 MAPK module can be activated by two upstream branches. One involves MEKKs Ssk2p and Ssk22p and a two-component histidine kinase phospho-relay system comprised of Sln1, Ypd1, and Ssk1. The other involves the activation of Pbs2 by Ste11 (Fig. 1), which functions downstream from Sho1 and Msb2 (112). In addition to its role in osmoregulation, the HOG pathway has recently been implicated in the response to nonosmotic stresses, such as arsenite, lower temperatures, and acid pH (89, 100, 115, 138). The other yeast MAPK is Smk1, a sporulation-specific MAPK activated by intracellular signals (50). It lacks upstream MEK or MEKK and has no homolog in other fungi except for some ascomycetous yeasts, such as Ashbya gossypii and Kluyveromyces lactis.


arrow
HOMOLOGS OF THE YEAST FUS3/KSS1 MAPKs
 
While fungi in the saccharomycetales, such as A. gossypii, K. lactis, and Candida albicans, have both Fus3 and Kss1 homologs, most filamentous fungi, like the archiascomycete Schizosaccharomyces pombe, have only one MAPK, which is homologous either to yeast Fus3 or to Kss1.

Ustilago maydis. The corn smut fungus U. maydis has been extensively studied for signal transduction pathways regulating mating and pathogenesis (for a review, see the work of Kahmann and Kamper [63]). It is a facultative biotrophic pathogen with a haploid, saprophytic yeast phase. Fusion of compatible yeast cells leads to the development of dikaryotic hyphae that can infect corn plants and cause tumors. The cAMP signaling pathway plays a critical role in regulating hyphal growth and pathogenic development. Strains blocked in the cAMP signaling pathway, such as the gpa3 (G{alpha} subunit), uac1 (adenylate cyclase), and adr (catalytic subunit of PKA) deletion mutants, are nonpathogenic and grow filamentously (10, 63). Mating recognition occurs between pheromones and receptors and results in the activation of a downstream MAPK cascade consisting of the MEKK Kpp4 (Ubc4), MEK Fuz7 (Ubc5), and MAPKs Kpp2 (Ubc3) and Kpp6. Fuz7, a homolog of yeast Ste7, is the first element of this cascade to be characterized. It is important for conjugation tube production, filamentous growth, tumor induction, and teliospore formation and germination.

Kpp2 (Ubc3) and Kpp6 are two MAPKs with overlapping functions in mating and plant infection (10, 63). The kpp2 (ubc3) mutant is defective in pheromone responses and the formation of filamentous dikaryons and reduced in virulence. Kpp6 contains an unusual N-terminal domain and plays a more critical role in appressorial penetration than Kpp2. The kpp6 mutant is reduced in virulence and defective in the penetration of plant cuticle (15). The kpp2 kpp6 double mutants are abolished in mating and nonpathogenic on maize plants. Because transformants expressing the kinase dead kpp6 allele and the unphosphorylatable kpp2 allele are more severely compromised in pathogenesis than the kpp6 and kpp2 mutants, respectively (106), the inactive kpp6 and kpp2 alleles may have additional inhibitory effects or downstream targets. Crk1 was first identified as a homolog of yeast Ime2 but later described as a novel MAPK in U. maydis that regulates morphogenesis, cell cycle, and plant infection (48). The crk1 mutant is defective in prf1 expression, mating, and plant infection.

The MEKK acting upstream from Fuz7 is Kpp4/Ubc4. Similar to fuz7 mutants, kpp4 deletion mutants are nonpathogenic and defective in the induction of pheromone-responsive genes (63). Deletion of Ubc2 (Ste50 homolog) also impairs pheromone responses and virulence (91). Different from other Ste50 homologs, Ubc2 has two C-terminal Src homology 3 domains that may be involved in protein-protein interactions. Ubc2 may function as an adaptor protein for the Kpp4-Fuz7-Kpp2/Kpp6 cascades. In U. maydis, the Smu1 PAK kinase is not directly involved in the activation of Kpp4 and downstream MAPKs, and it is dispensable for mating, plant infection, or tumor formation (134).

Ras2, one of the Ras proteins in U. maydis, has been placed upstream from Kpp4 and Ubc2. Mutation in the ras2 gene suppresses a constitutively filamentous phenotype of the adr1 mutant (80). Expression of a dominant active ras2 allele promotes pseudohyphal growth in a manner dependent on the Ubc4-Fuz7-Ubc3 cascade. In contrast, constitutive activation of Ras1 increases the expression of mfa1 but has no effect on cell morphology and yeast growth (104). Therefore, Ras2 and Ras1 in U. maydis may affect the MAPK and the cAMP-protein kinase A (PKA) pathway, respectively. A potential activator of Ras2 is the Cdc25-like guanine exchange factor protein Sql2 (104). However, unlike the ras2 mutant, the sql2 deletion mutant is defective in plant infection but not in mating. Sql2 may be an in planta-specific activator of Ras2 in response to lipid signals for promoting and maintaining filamentous growth (68). Although Gpa3 is essential for pheromone signaling and pathogenic development, the pheromone receptors Pra1 and Pra2 have not been functionally linked with any of the four G{alpha} submits in U. maydis. The Gß subunit Bpp1 is involved in the cAMP-PKA pathway, but it is not an effector for the MAPK cascade (105).

The HMG-domain transcription factor Prf1 is required for mating and plant infection. It has consensus MAPK and PKA phosphorylation sites and interacts with Adr1 as well as MAPK Kpp2 in vivo (62). While the PKA phosphorylation sites of Prf1 are essential for the induced expression of both a and b mating type genes, the MAPK phosphorylation sites are required only for b gene expression. Another HMG-domain protein, Rop1, is involved in mating, filamentous growth, and regulation of prf1 expression in axenic cultures. However, Rop1 is dispensable for conjugation, prf1 expression, and virulence on maize plants (17). In addition, Prf1 is not required for Kpp4 to control conjugation tube formation (106). Acidic pH still induces the yeast-to-hypha transition in haploid cells of the prf1 mutant but not the ubc4 or fuz7 mutant (90). Therefore, an additional transcription factor(s) may function downstream from this MAPK pathway for regulating responses to different signals and filamentous growth.

Magnaporthe grisea. Rice blast caused by M. grisea is one of the most severe fungal diseases of rice throughout the world. The fungus develops specialized infection structures called appressoria and uses the enormous turgor pressure generated in appressoria for plant penetration. While surface recognition and the initiation of appressorium formation are mediated by the cAMP signaling, late stages of appressorium formation and penetration are regulated by the PMK1 pathway. The pmk1 deletion mutant fails to form appressoria but still recognizes hydrophobic surfaces and responds to cAMP (151). PMK1 also is essential for infectious hyphal growth after penetration. In transformants expressing a PMK-green fluorescent protein construct, enhanced green fluorescent protein signals and nuclear localization are observed in appressoria and developing conidia (18).

Several upstream components of the PMK1 pathway, including the MEKK Mst11 and the MEK Mst7 and an Ste50 homolog, Mst50, have been characterized (118, 158). The mst7, mst11, and mst50 mutants fail to form appressoria and are nonpathogenic. Mst50 directly interacts with both Mst7 and Mst11 and may function as an adaptor protein for the Mst11-Mst7-Pmk1 cascade. The direct interaction of Mst7 with Pmk1 is mediated by the docking site and occurs specifically during appressorium formation (159). MST20, a homolog of yeast STE20, is dispensable for PMK1 activation in M. grisea (85). Consistent with this observation, the CDC42 homolog in M. grisea is dispensable for appressorium formation and plant infection (S. Wu and Z. Wang, personal communication). Therefore, unlike the yeast pheromone response pathway, PAK kinase and MgCdc42 are not essential for activating the Pmk1 MAPK cascade in M. grisea.

Mst50 and Mst11 both interact with Ras1 and Ras2, two Ras proteins in M. grisea (118). The ras1 deletion mutant has no defect in plant infection and appressorium formation, but RAS2 appears to be an essential gene. Expression of a dominant active RAS2 allele in the wild-type strain but not in the pmk1 mutant stimulates appressorium formation on nonconducive surfaces (118), indicating that RAS2 functions upstream from the Mst11-Mst7-Pmk1 cascade. In addition, the G{alpha} subunit MagB, Gß subunit Mgb1, and a negative regulator of G-protein signaling (Rgs1) have been implicated in regulating appressorium formation (86, 87, 110). Exogenous cAMP induces appressorium formation in mgb1 mutants, but these appressoria are morphologically abnormal and nonfunctional. MGB1 may control surface recognition via the cAMP signaling but function through the PMK1 pathway to regulate appressorial penetration and invasive growth.

The M. grisea genome has no recognizable receptor protein kinase genes but contains a large number of GPCR-like genes (75), including putative homologs of Ste2, Ste3, GprD, and Pre-1. Twelve of them form a subfamily containing the CFEM domain, which is unique to fungi (32). In M. grisea, deletion of the yeast Ste2 and Ste3 homologs has no obvious effects on appressorium formation or plant infection (J.-R. Xu, unpublished data), but one putative CFEM-GPCR gene, PTH11, has been implicated in surface recognition via cAMP signaling (35). However, exogenous cAMP restores appressorium formation and pathogenicity in the pth11 mutant, suggesting that PTH11 may be involved in the regulation of cAMP signaling. Also, predicting GPCRs is not reliable, and there is no direct evidence to support the sensory role of Pth11 in M. grisea.

One putative downstream transcription factor regulated by Pmk1 is Mst12 (Ste12 homolog), which is essential for pathogenesis. Appressoria formed by the mst12 mutant have normal appressorium turgor but fail to develop penetration pegs, probably due to cytoskeleton defects in mature appressoria (117). MST12 may regulate genes involved in penetration and infectious growth, but another transcription factor(s) must function downstream of PMK1 for regulating appressorium formation. One of the REMI mutants defective in appressorium formation is disrupted in a homeobox gene, PTH12. However, the pth12 deletion mutant still occasionally forms melanized appressoria and responds to exogenous cAMP for appressorium formation (Y. Peng, personal communication). Several genes regulated by PMK1 have been identified by subtractive hybridization, including GAS1 and GAS2, two homologous genes that are unique to filamentous fungi and specifically expressed during appressorium formation (153).

Other plant pathogenic fungi. (i) Appressorium-forming pathogens. Homologs of FUS3/KSS1 in several other plant pathogenic fungi that form well-developed appressoria, including Cochliobolus heterostrophus, Colletotrichum lagenarium, C. gloeosporioides, and Pyrenophora teres, have been characterized. In all these fungi, PMK1 homologs are essential for appressorium formation (128, 151). Similar to the pmk1 mutant, the P. teres ptk1 and C. lagenarium cmk1 mutants are nonpathogenic and fail to colonize healthy or wounded host tissues. Conidia of the cmk1 mutant fail to germinate on plant and glass surfaces. In contrast, the STE12 homolog is essential for penetration and infectious growth but dispensable for appressorium formation in C. lagenarium (139). In the rice leaf spot pathogen Bipolaris oryzae, BMK1 is required for plant infection and conidiation, but its role in appressorium formation and penetration has not been examined (101).

In C. heterostrophus, CHK1 is important for invasive growth and efficient colonization of leaf tissue after penetration, but the chk1 mutant still forms a few small, restricted lesions on corn leaves. Other phenotypes of the chk1 mutant include reduced aerial hyphae, autolysis, lack of conidiation, and loss of female fertility (83). Genes for cellobiohydrolase Cbh1, for endoglucanase Eg6, for transcription factor Cmr1, and for three enzymes for melanin synthesis are among those known to be regulated by Chk1 (43, 82). Similar to CHK1, the CGB1 (Gß) gene is essential for appressorium formation, female fertility, hyphal pigmentation, and full virulence (47). However, the cgb1 mutant still produces conidia and is more severely reduced in virulence than the chk1 mutant. Deletion of CGA1 (G{alpha}) reduces appressorium formation but has no effect on pathogenesis, suggesting that CGB1 and other upstream components, but not CGA1, may function upstream from the Chk1 cascade.

(ii) Non-appressorium-forming foliar pathogens. The PMK1 homologs also are essential for infection in two foliar pathogens of wheat, Mycosphaerella graminicola and Stagonospora nodorum. In M. graminicola, the MgFus3 deletion mutant is nonpathogenic and fails to colonize the mesophyll tissue through stomata (30). MgFUS3 is important for aerial hyphal growth, melanization, and pycnidium formation. Similar to what is seen for the mst20 mutant in M. grisea, deletion of a putative STE20 homolog has no obvious effect on the vegetative growth or virulence of M. graminicola (30). In S. nodorum, mak2 disruption mutants have reduced growth rates and are defective in conidiation, but they have no significant changes in the level of secreted protease activity, osmotic stress response, or melanin synthesis (135). Although mak2 mutants fail to form penetration structures and are essentially nonpathogenic, they are able to enter the leaf via natural openings. However, the infection progress and the ability to cause disease once inside the leaf are compromised in the mak2 mutant, which causes only limited necrosis on leaves (135).

(iii) Root or vascular pathogens. In Fusarium oxysporum f. sp. lycopersici, the fmk1 mutant displays normal growth and conidiation but is nonpathogenic on tomato plants and significantly reduced in the expression of the pectate lyase gene PL1 (37). FMK1 is dispensable for conidium germination but is required for the differentiation of penetration hyphae and root attachment. In the vascular wilt pathogen Verticillium dahliae, vmk1 mutants are nonpathogenic on a variety of host plants tested and defective in microsclerotium production (123). Interestingly, PMK1 is also required for root infection in M. grisea, and it can functionally complement the fmk1 mutant (37), suggesting a conserved role for this MAPK pathway in soilborne and foliar pathogens. A FMK1 homolog from Tuber borchii is phosphorylated during plant colonization and partially restores invasive growth of the fmk1 mutant. Therefore, the same MAPK pathway may regulate the establishment of symbiosis and ectomycorrhizae (95).

The fgb1 (Gß) deletion mutant of F. oxysporum also is reduced virulence, but it has an unaltered Fmk1 phosphorylation level and is defective in hyphal growth (33). Exogenous cAMP reverses part but not all of the fgb1 growth phenotypes. Therefore, Fgb1 may act upstream from the cAMP signaling but not the Fmk1 pathway. In infection assays with an immunodepressed mouse model, the fmk1 fgb1 double mutant but not the fmk1 mutant or the fgb1 mutant is significantly reduced in virulence (121). Fmk1 and Fgb1 appear to be components of distinct signaling pathways with overlapping functions.

(iv) Necrotrophic pathogens. PMK1 homologs are also important for pathogenesis in several other necrotrophic ascomycetes (Table 1). In Botrytis cinerea, the bmp1 mutant has a reduced growth rate and is nonpathogenic. Germ tubes of the bmp1 mutant fail to penetrate the host tissue (160). Recently, an independent bmp1 mutant was reported to be defective in conidium germination on hydrophobic surfaces and in responding to carbon sources (39). Differences in conidium germination between two bmp1 mutants may be related to different spore concentrations used or mutant backgrounds. In Alternaria brassicicola, amk1 mutants are nonpathogenic on intact plants but still colonize wounded leaves in the presence of nutrient supplements. Amk1 is essential for the production of mature conidia and up-regulation of several hydrolytic enzyme genes (26). In Cryphonectria parasitica, the cpmk2 deletion mutant is defective in conidiation and pheromone production and has reduced growth rate and canker size (27). Although the activation of CpMK2 is not affected, CpSTE12 is down-regulated by hypovirus infection (34). Many genes affected by the hypovirus are down-regulated in the cpste12 mutant, which is reduced in virulence and female sterile (34). In Sclerotinia sclerotiorum, Smk1 regulates sclerotium development, but its role in plant infection has not been determined (24).


View this table:
[in this window]
[in a new window]

  		TABLE 1. FUS3/KSS1 homologs in pathogenic fungi

In the wheat scab fungus F. graminearum, the gpmk1 (map1) deletion mutants are reduced in conidiation, female sterile, and nonpathogenic (57, 140). The gpmk1 mutants are impaired in colonizing wheat heads and spreading from inoculated florets to neighboring spikelets. They also fail to infect roots, wounded wheat floral tissues, and tomato fruits but still produce phytotoxic deoxynivalenol. Gpmk1 regulates the early induction of extracellular endoglucanase, xylanolytic, and proteolytic activities and is responsible for the overall induction of secreted lipolytic activities (58). One of the genes regulated by Gpmk1 is FGL1, which encodes a secreted lipase and is an important virulence factor in F. graminearum (144).

(v) Biotrophic pathogens. The cpmk1 mutant of Claviceps purpurea has no defect in vegetative growth or conidiation but is incapable of penetration and nonpathogenic on rye plants (97). Mutants deleted of the CDC42 homolog in C. purpurea also are nonpathogenic, but they still penetrate the stylar tissue. The invasive growth of the CpCdc42 mutant is arrested at an early infection stage, presumably due to induced plant defense responses (131). Expression of CPMK1 in the pmk1 mutant fully complements its defects, indicating that this MAPK pathway is functionally conserved between hemibiotrophic and biotrophic pathogens. In the barley powdery mildew fungus Blumeria graminis, both a MAPK and the cAMP signaling are involved in regulating appressorium development (67). In another obligate biotroph, Puccinia triticina, the PtMAPK1 gene has increased expression levels during urediospore germination and plant infection. When expressed in U. maydis, it complements the defect of kpp2 mutants in mating and plant infection (56).

Model saprophytic filamentous fungi. In the model filamentous fungus Neurospora crassa, mutants deleted of the MEKK NRC-1 and MAPK MAK-2 genes have the same pleiotropic phenotype, including derepressed conidiation, shortened aerial hyphae, lack of hyphal fusion and conidial anastomosis tube, female sterility, and flattened ascospores (72, 116). The pp-1 (Ste12 homolog) deletion mutant has similar defects (84). However, none of the individual GPCR, G{alpha}, Gß, or G{gamma} deletion mutants are phenotypically similar to the mak-2 mutant.

Unlike other filamentous fungi, several Aspergillus species, including A. niger, A. nidulans, and A. fumigatus, have four MAPK genes (124). The two MAPKs with the TEY dual phosphorylation site, MpkA and MpkB, are homologous to yeast Slt2 and Kss1, respectively. Although MpkB has not been functionally characterized, SteA (Ste12 homolog) is required for the development of ascogenous hyphae and cleistothecia. The steA deletion mutant is blocked in sexual reproduction but has normal vegetative growth and conidiation (141). However, the steC (Ste11 homolog) deletion mutant has a pleiotropic phenotype, including a reduced growth rate, altered conidiophore morphology, and defects in heterokaryon formation and cleistothecium development (148).

Candida albicans. C. albicans causes various forms of candidiasis, particularly in immunocompromised patients. The reversible dimorphic transition between the yeast form and the hyphal form is important for its virulence and can be triggered by various signals in vitro, including high temperature, neutral pH, and serum. C. albicans also occasionally undergoes switching between white-phase cells that form dome-shaped, white colonies and opaque-phase cells that are more elongated and form flatter, darker colonies on solid agar. Signal transduction pathways regulating filamentous growth and the white-opaque switching have been well studied for C. albicans (for reviews, see the work of Alonso-Monge et al. [2], of Bennett and Johnson [11], and of Chen et al. [25]).

The Cek1 (Kss1 homolog) MAPK cascade has been well characterized for its role in the yeast-hypha transition and virulence (2, 11). Homozygous cek1 mutants are defective in transition from unicellular budding growth to invasive hyphal growth on Spider or synthetic low-ammonium-dextrose (SLAD) medium and are significantly attenuated in virulence with murine models for systemic or superficial candidiasis. All the major components of the yeast pheromone response pathway except Ste5 have been identified in C. albicans (11). The PAK kinase Cst20, MEK Hst7, Cph1 (Ste12 homolog), CaTec1, CaRas1, Cdc42, and its exchange factor Cdc24 are also required for hyphal morphogenesis, invasive hyphal growth, and virulence. The defect of the CaRas1 deletion mutant in morphological transition is suppressed by exogenous cAMP or overexpression of CEK1 (78), indicating that CaRas1 functions in both signaling pathways.

All the mutants blocked in the CEK1 pathway, however, are still capable of filamentous growth in response to serum. Multiple signaling pathways, including the cAMP-dependent protein kinase pathway via Efg1, a pH-responsive pathway through Rim101, and Tup1-mediated repression through Rfg1 and Nrg1, are known to regulate hyphal development and infection processes in C. albicans (2, 61). Cph1 and Efg1 have overlapping functions for induced expression of genes responsive to serum, and the homozygous cph1 efg1 double mutant fails to develop hyphae or pseudohyphae in response to many stimuli (16, 88). Unlike Tec1 in yeast, CaTec1 is regulated by Efg1 and the basic helix-loop-helix transcription factor Cph2 but not by Cph1 in C. albicans (77). Recently, the Mep2 ammonium permease has been shown to mediate the induction of filamentous growth in response to nitrogen starvation by its interaction with CaRas1 (13).

Although C. albicans is a diploid fungus traditionally classified as asexual, mating between genetically modified strains and a parasexual cycle have been observed. CEK2 (25) and several components of the CEK1 pathway, including STE2, GPA2, CST20, HST7, CEK1, and CPH1 (2), are involved in mating responses. CEK2 encodes a MAPK highly similar to that encoded by FUS3. It is dispensable for filamentous growth on artificial media but has overlapping functions with CEK1 in mating. While the cek1 and cek2 deletion mutants are reduced in mating efficiency, cek1 cek2 double mutants, like the hst7 and cph1 mutants, are completely blocked in mating (25). For upstream components, the GPCR gene STE2 is essential for mating responses to the alpha pheromone, and the Gpa2 G{alpha} subunit is involved in relaying nutrient signals to mating. In S. cerevisiae, Mcm1 is involved in cell type-specific transcription and pheromone response. Overexpression of CaMCM1 induces the expression of a hypha-specific gene HWP1 and hyphal development, but its function in mating is not clear in the case of C. albicans (126). The Cph1-mediated MAPK pathway is involved in the regulation of white-opaque switching, which is controlled by the mating type locus (2, 98). Unlike the yeast pheromone response pathway, Cek1appears to be activated by quorum sensing and other environmental signals (125, 130). Farnesol, a quorum-sensing molecule, reduces the transcription levels of HST7 and CPH1 in C. albicans. Diluting stationary-phase cells in fresh rich medium also stimulates the phosphorylation of Cek1. In C. albicans, Sho1 is essential for Cek1 activation under different conditions that require active cell growth and cell wall remodeling (125). The sho1 mutant is sensitive to oxidative stress and cell wall-interfering compounds (Congo red and calcofluor white) and is defective in morphogenesis on SLAD and Spider media, which stimulate hyphal growth (125). These results reveal a role for Sho1 in linking oxidative stress, cell wall biogenesis, and morphogenesis in C. albicans.

Cryptococcus neoformans. C. neoformans is the causal agent of cryptococcal meningoencephalitis. Mating between MAT{alpha} and MATa cells on a nutrient starvation medium leads to the formation of dikaryotic filaments. The mating type locus contains mating type-specific Ste11 and Ste12 homologs, but the Cpk1 MAPK and Ste7 homolog are not linked to the mating type locus (31). The cpk1 and ste7 deletion mutants of both mating types are severely impaired in mating but not completely sterile. The cpk1{alpha}, ste7{alpha}, and ste11{alpha} mutants are also blocked in haploid fruiting (29, 31). However, the ste11{alpha}, ste7, and cpk1 mutants are as virulent as the wild-type strains in a disseminated mouse model, indicating that the CPK1 MAPK pathway is important for mating and haploid fruiting but dispensable for virulence.

While the Gpa1 G{alpha} subunit plays a critical role in the cAMP signaling, the Gpb1 Gß subunit functions upstream from the CPK1 cascade. The mating defect of the gpb1 mutant is suppressed by overexpression of CPK1 but not exogenous cAMP (146). The gpb1 mutant also is defective in haploid fruiting, which can be suppressed by the overexpression of Ste12{alpha}. Therefore, mating and haploid fruiting in C. neoformans are mediated by GPB1 via the CPK1 MAPK cascade (146). A Ras homolog has also been identified as an upstream component of this pathway. The ras1 mutant is viable but unable to grow at 37°C, defective in mating, and avirulent in a rabbit model of cryptococcal meningitis. It has no defects in melanin and capsule production, which are two events regulated by Gpa1-cAMP signaling (4, 147). Expression of a dominant active RAS1 (RAS1Q67L) allele enhances haploid fruiting in serotype A strain H99 but not in the ste12{alpha} mutant (3, 156). Although the mating defect of the gpb1 mutant is not recovered by the RAS1Q67L allele, expression of a dominant GPB1 allele rescues the mating defect of the ras1 mutant, indicating that RAS1 functions upstream of GPB1 in the mating process (4, 81). Several GPCR genes in C. neoformans, including Ste3a, Ste3{alpha}, and Gpr4, have also been characterized. The Ste3 homologs are important for mating and have a mating type-specific role in virulence (20). Gpr4 is dispensable for infection, but it may function as an amino acid sensor and interact with Gpa1 for regulating the cAMP-PKA pathway (154).

Ste12{alpha} may function downstream of Cpk1 because overexpression of Ste12{alpha} suppresses the defects of the cpk1 mutant in mating and haploid fruiting. However, overexpression of Ste11{alpha} or Cpk1 can restore haploid fruiting in the ste12{alpha} mutant, suggesting that Ste12{alpha} does not function downstream from Cpk1 in a strictly linear pathway (31). Interestingly, Ste12{alpha} and Ste12a are important for virulence in a serotype-specific manner. Unlike the ste11a, ste7, and cpk1 mutants, the ste12 mutants in serotype D are significantly reduced in virulence (22, 156). In contrast, the PAK kinase Ste20{alpha} contributes to virulence in serotype A but not in serotype D strains (145).

Other human pathogenic fungi. The FUS3/KSS1 homologs have been identified in several other human pathogens, including A. fumigatus, Penicillium marneffei, and Pneumocystis carinii (44). However, their function in pathogenesis has not been characterized. In P. carinii, phosphorylation assays and expression analyses of a few candidate components of the PCM MAPK pathway, including PcSte11, PcSte20, and PcSte3, have suggested that this MAPK pathway may play regulatory roles in the life cycle and infection processes of this opportunistic pathogen (143). In P. marneffei, StlA (Ste12 homolog) is dispensable for asexual development and dimorphic switching but can complement the sexual reproduction defect of the A. nidulans steA mutant (14).


arrow
CELL WALL INTEGRITY PATHWAY
 
Several orthologs of yeast SLT2 in plant and human pathogens have been characterized. In general, this MAPK pathway is important for pathogenesis and cell wall integrity.

Plant pathogenic fungi. The MPS1 MAPK is essential for conidiation, appressorial penetration, and plant infection in M. grisea (152). The mps1 deletion mutant is significantly reduced in aerial hyphal growth and conidiation, but it displays no obvious changes in the growth rate. Unlike Pmk1, Mps1 is dispensable for appressorium formation. Appressoria formed by the mps1 mutant fail to penetrate and develop infectious hyphae but still elicit plant defense responses. Vegetative hyphae of the mutant have a weakened cell wall, undergo autolysis in aging colonies, and are hypersensitive to cell wall-lytic enzymes (152). The M. grisea genome contains distinct homologs of many components of the yeast Pkc1-Slt2 pathway (32), including Pkc, Bck1, Mmk2, Rom2, Rlm1, and Swi6. However, it lacks significant homologs of the receptor genes of the yeast Pkc1-Slt2 pathway except for one gene with limited homology to Wsc1 (e-value, 1e-4). Receptors may not be well conserved, and M. grisea may have novel receptors for recognizing plant or environmental signals.

Functional characterization of the SLT2 homolog in several other plant pathogenic fungi (Table 2) has indicated that this MAPK is well conserved among fungal pathogens and plays important roles during plant infection. In C. lagenarium, MAF1 is required for the early stages of appressorium formation (70). Elongated germ tubes of the maf1 mutant fail to form appressoria. In C. purpurea, CPMK2 also is necessary for penetration, and the cpmk2 mutant retains only a limited ability to colonize host tissues (96). In M. graminicola, mgslt2 mutants are normal in penetration of stomata but fail to colonize and grow invasively in plants (92). The bmp3 mutant of B. cinerea is defective in penetrating dead onion epidermal cells and developing necrotic lesions (127). In F. graminearum, the mgv1 mutant is reduced in deoxynivalenol accumulation (55) and hypersensitive to plant defensin MsDef1 (122). Mgv1 also is essential for hyphal fusion and heterokaryon formation (55).


View this table:
[in this window]
[in a new window]

  		TABLE 2. SLT2 homologs in pathogenic fungi

In contrast to its conserved role in pathogenesis, the function of this MAPK in cell wall integrity, conidiation, and stress responses varies among fungal pathogens. Similar to the mps1 mutant, the cpmk2 and mgv1 mutants in C. purpurea and F. graminearum have weakened cell walls and increased susceptibility to cell wall-lytic enzymes and certain compounds that interfere with the cell wall, such as nikkomycin Z (a chitin synthase inhibitor) and calcofluor white (55, 96). In contrast, deletion of the SLT2 ortholog has no obvious effect on sensitivities to cell wall-lytic enzymes and inhibitors in M. graminicola and B. cinerea (127). Interestingly, the Mgslt2 mutant is hypersensitive to several azole fungicides, including miconazole and cyproconazole. The bmp3 mutant has increased sensitivity to paraquat and the phenylpyrrole fungicide fludioxonil, but it is not hypersensitive to the azoles, elevated temperatures, or H2O2 (127).

The SLT2 orthologs are also required for conidiation in C. lagenarium and C. purpurea. However, conidiation is normal in the mgv1 mutant of F. graminearum and the mgslt2 mutant of M. graminicola (Table 2). The bmp3 mutant of B. cinerea produces fewer macroconidia but more microconidia than the wild type (127). It also is defective in sclerotium formation and germ tube responses to surfaces. Unlike the pmk1, maf1, and mgslt2 mutants, the mgv1 and bmp3 mutants exhibit reduced growth rates on solid media. However, vegetative growth in liquid cultures is normal in the mgv1 mutant. The pleiotropic phenotypes observed for these mutants indicate that this MAPK pathway may regulate various growth or differentiation processes in different plant pathogenic fungi.

Model saprophytic filamentous fungi. In A. nidulans, MpkA plays an important role in conidium germination and hyphal tip growth. The mpkA mutant has a reduced growth rate, and its hyphal tips tend to swell (19). Conidia often grow isotropically and fail to produce germ tubes under normal culture conditions. In Podospora anserina, crippled growth is an epigenetic cell degeneration phenomenon caused by C, a cytoplasmic and infectious hereditary unit that resembles a prion. PaASK1, a BCK1 homolog, is required for C production. The paask1 mutant is defective in hyphal pigmentation, differentiation of aerial hyphae, and fruiting body development. Mutants deleted of the downstream MEK PaMkk1 or MAPK PaMpk1 have the same phenotype as the paask1 mutant (65). Overexpression of PaASK1 or PaMPK1 facilitates C propagation and enhances crippled growth in wild-type strains. The activation and nuclear localization of PaMpk1 appear to be correlated with the presence of the C element in vegetative hyphae (65). The autolysis and pigmentation defects of the mps1 mutants of M. grisea and C. heterostrophus may be related to cell degeneration.

Human pathogens. In C. albicans, Mkc1 (Slt2 homolog) is involved in regulating cell wall integrity and required for growth at elevated temperatures (109). Homozygous mkc1 deletion mutants exhibit increased susceptibility to caffeine, glusulase, and some inhibitors of cell wall synthesis. Growth rates and cell viabilities of mkc1 mutants are reduced in cultures grown at 42°C. In addition, Mkc1 has been implicated in morphological transitions and pathogenesis (36, 107). The mkc1 mutants are also reduced in invasive growth on Spider medium and produce shorter hyphal cells (for a review, see the work of Alonso-Monge et al. [2]). In infection assays with a murine model, mkc1 mutants are attenuated in virulence. The mkc1 mutants have increased sensitivities to nitric oxide (NO) in in vitro assays and reduced abilities to inhibit NO production by macrophages (99).

The Mkc1 pathway is also involved in responses to other stresses. The activation of Mkc1 is triggered by various oxidants, certain osmotic stresses, antifungal drugs targeted at cell wall and membrane syntheses, calcium ion, and low-temperature shock (108). The phosphorylation of Mkc1 in response to oxidative stress is partially dependent on the CaHOG1 pathway (5), suggesting cross talk between these two pathways. The activation of Mkc1 by oxidative stress is blocked in the capkc1 mutant (108), indicating that C. albicans has a similar PKC-Slt2 cell wall integrity pathway. The capkc1 deletion mutants are normal in the yeast-to-hypha transition but have an osmotically remediable cell lysis defect. Cercosporamide, a selective inhibitor of Pkc1, has synergistic fungicidal effects with caspofungin (a ß-1,3-glucan synthase inhibitor) in C. albicans (136). In S. cerevisiae, Wsc1 acts as the dedicated sensor for caspofungin-induced cell wall damage to activate the Pkc1-Slt2 pathway. Short exposure to caspofungin results in the up-regulation of MKC1, and the mkc1 mutant has increased sensitivity to caspofungin (149). Mkc1 is also activated by physical contact in C. albicans. The mkc1 mutants are defective in invasive hyphal growth on YPS agar and normal biofilm formation, two contact-dependent responses (76).

In C. neoformans, the MPK1 MAPK gene is required for growth at elevated temperatures and the maintenance of cell wall integrity (73). The growth defect of the mpk1 deletion mutant at 37°C can be remedied by an osmotic stabilizer such as 1 M sorbitol. Phosphorylation of Mpk1 is induced by antifungal compounds nikkomycin Z and caspofungin. The mpk1 mutant is significantly attenuated in virulence and hypersensitive to fludioxonil or cell wall synthesis inhibitors, but it is normal in the production of melanin and capsule (69, 73). The growth defect at 37°C and weakened cell wall of the mpk1 mutant may be responsible for its reduced virulence.

Several other components of the putative Pkc1-Mpk1 pathway in C. neoformans, including homologs of yeast Rho1, Bck1, Mkk2, Lrg1, Rom2, Rom20, and Rom21, have been characterized, but their functions in virulence remain to be examined (21, 49). Although both Bck1 and Mkk2 homologs are critical for maintaining cell wall integrity and growth at elevated temperatures, the mkk2 but not the bck1 deletion mutant is reduced in melanin production. Inhibition of Pkc1 abolishes melanin synthesis in C. neoformans (53). Deletion of the phosphatase Ppg1 also reduces melanin production, but ppg1 mutants have additional defects, such as reduced capsule size. While ROM2 is dispensable, Lrg1 and two other genes (SSD1 and PUF4) are important for cell wall integrity in C. neoformans, which lacks homologs of several yeast membrane-associated stress sensors (49). Therefore, the regulatory mechanisms for maintaining cell wall integrity in S. cerevisiae and C. neoformans appear to be different. The C. neoformans genome also lacks significant homologs of several yeast membrane-associated stress sensors, including Slg1, Wsc2, and Mid2 (49).

The Slt2 homolog has been identified but not functionally characterized for several other human pathogens, including A. fumigatus, P. carinii, P. marneffei, Histoplasma capsulatum, Blastomyces dermatitidis, and Coccidioides posadasii. In P. carinii, expression of the MKP1 MAPK gene and PcBCK1 can partially complement the yeast slt2 and bck1 mutants, respectively (45, 137), but their functions in P. carinii are not clear. Mkp1 contains a unique phosphorylation motif repeat (TEYMTEY). Dual phosphorylation of Mkp1 at T186 and Y188 is required for its kinase activity but not for its ability to partially complement the slt2 mutant and interact with the transcription factor Rlm1 (45).


arrow
OSMOREGULATION/STRESS RESPONSE PATHWAY
 
Hog1 and its homologs in filamentous fungi have the TGY dual phosphorylation site, a hallmark of stress-activated MAPKs. While Hog1 has limited functions besides osmoregulation in S. cerevisiae, its homolog in pathogens is involved in pathogenesis and response to various stresses.

Plant pathogenic fungi. Unlike what is seen for the other two MAPKs, the role of HOG1 homologs in pathogenesis differs drastically among plant pathogens, probably due to differences in host defensive responses or infection mechanisms. In M. grisea, OSM1 is dispensable for plant infection (38). Although the osm1 mutant is hypersensitive to desiccation and hyperosmotic stress, it has no defect in conidiation and appressorium function. In the presence of 0.4 M NaCl, conidia of the osm1 mutant form multiple appressoria, suggesting that OSM1 suppresses inappropriate activation of the PMK1 pathway under hyperosmotic conditions. Deletion of histidine kinase gene HIK1, homologous to OS-1, also has no effect on appressorium function and virulence (103). Unlike the N. crassa os-1 mutant, the hik1 mutant is more sensitive to high concentrations of sugars but not salts, suggesting that M. grisea can distinguish between hyperosmotic stresses caused by these compounds.

Mutants deleted of the HOG1 homolog in C. parasitica, Bipolaris oryzae, C. lagenarium, and M. graminicola also are sensitive to hyperosmotic stresses (71, 93, 102, 119). While the osc1 and srm1 deletion mutants of C. lagenarium and B. oryzae are fully pathogenic, the M. graminicola mghog1 mutant and the B. cinerea bcsak1 mutant are nonpathogenic (Table 3). The mghog1 mutant fails to switch to filamentous growth on water agar plates and is defective in melanization and formation of infectious germ tubes (93). In B. cinerea, macroconidiation but not microconidiation is regulated by BcSak1. The bcsak1 mutant is derepressed in sclerotium formation but blocked in appressorium formation and plant penetration (133). In C. parasitica, cpmk1 mutants are reduced in virulence and form cankers smaller than those formed by the wild-type strain (119). In several plant pathogenic fungi, this MAPK pathway also regulates responses to oxidative stress and UV irradiation (71, 102). In general, deletion of the Hog1 homolog increases the sensitivity to various oxidants.


View this table:
[in this window]
[in a new window]

  		TABLE 3. HOG1 homologs in pathogenic fungi

In several filamentous fungi, including N. crassa, C. lagenarium, and M. grisea, mutants blocked in the HOG pathway are resistant to phenylpyrrole, dicarboximide, and aromatic hydrocarbon fungicides (71, 103, 157). Treatments with these fungicides stimulate the activation of the Hog1 homolog, glycerol accumulation, and cell swelling or bursting, indicating that fungicidal effects may result from the overstimulation of the osmoregulation pathway. In B. cinerea, the bcsak1 mutant is resistant to dicarboximide but still sensitive to phenylpyrrole or aromatic hydrocarbon fungicides. In contrast, the deletion of BOS1 (OS-1 homolog) confers resistance to all these fungicides. The bos1 mutant also differs from the sak1 mutant in virulence and appressorium formation (133, 142). Phenotypic differences between the bos1 and bcsak1 mutants may be related to the isolates used in these studies, but it is also possible that the HOG pathway in B. cinerea is more complex than that of other fungi.

Model saprophytic filamentous fungi. In N. crassa, the Os-2 MAPK cascade plays an important role in osmoregulation, fungicide resistance, and response to oxidative stress (111, 157). Unlike Os-4 (MEK) and Os-5 (MEKK), Os-1 is required only for Os-2 activation by fludioxonil or low osmotic stress. Phosphorylation of Os-2 is still detectable in the os-1 mutant by hyperosmolarity or heat shock (111), suggesting the involvement of other osmosensors. For the two putative response regulators, only Rrg-1 functions upstream from the Os-2 cascade for osmoregulation (59). Rrg-2 is dispensable for osmoregulation but is involved in response to oxidative stress (8).

In A. nidulans, SakA (HogA) is involved in the repression of sexual development, survival of conidia, and response to hyperosmotic and oxidative stresses (51, 64). Under hyperosmotic conditions, reduced growth rate, hyperbranching, abnormal nuclear distribution, and lack of septation near hyphal tips are observed in the sakA mutant incubated at 30°C. However, the same growth and branching defects are not detectable when the mutant is cultured at 37°C. A. nidulans must have an additional gene(s) involved in regulating response to osmotic stress. One candidate is MpkC, which is also activated by Pbs2. Although the deletion of MpkC has no obvious effect on stress response, the sakA mpkC double mutant may be nonviable (46).

Human pathogens. The HOG1 homologs have been implicated in responses to oxidative and hyperosmotic stresses in a few human pathogens. In C. albicans, CaHog1 is activated by various stress conditions, including high osmolarity, salts, oxidants, heavy metals, farnesol, and UV irradiation (for a review, see the work of Alonso-Monge et al. [2]). Several upstream components of the CaHog1 pathway have also been characterized, including PBS2, SSK1, and SHO1 (5, 23, 125). Activation of Hog1 by oxidative stress is Pbs2 dependent and is mediated by the Ssk1 branch. Because ssk1 sho1 double mutants still respond to hyperosmotic stress and grow on high-osmolarity media, additional upstream input may exist in C. albicans for CaHog1 activation. Among three putative C. albicans histidine kinase genes, NIK1, CHK1, and SLN1, that have been characterized, none has a clearly defined role in CaHog1 activation (2, 74). Although the deletion of SLN1 results in the constitutive activation of CaHog1 and a lower growth rate, the sln1 mutant, similar to the nik1 mutant, is viable when grown under hyperosmotic conditions. Chk1 regulates responses to oxidative stress and but is dispensable for Hog1 activation.

The CaHOG1 pathway also plays a role in cell wall biosynthesis and integrity. The cahog1 and capbs2 deletion mutants have increased susceptibility to ß-1,3-glucanases and are defective in chlamydospore formation (1, 42). Approximately 25% of genes with altered expression levels in the ssk1 mutant are related to cell wall and stress adaptation functions, including CHK1, HSP12, AHP1, and FLO1 (23). In addition, the CaHOG1 pathway has a repressive effect on filamentous growth, and it is important for pathogenesis (2). The cahog1 and capbs2 mutants are derepressed in hyphal formation, resistant to iprodione and fludioxonil, and reduced in virulence, probably due to the increased sensitivity to oxidative stress generated by the host immune cells. The ssk1 deletion mutant is hypersensitive to oxidative stress and human neutrophils and avirulent in an invasive murine model (94). Although their molecular mechanisms remain to be determined, the NIK1, CHK1, and SLN1 histidine kinase genes all are required for virulence and cell wall integrity in C. albicans (for a review, see the work of Kruppa and Calderone [74]).

In C. neoformans, Pbs2 and Hog1 are functionally conserved for regulating responses to UV radiation and hyperosmotic stress in both a highly virulent serotype A stain, H99, and a less virulent serotype D strain, JEC21. However, their functions in responses to elevated temperature (40°C) and oxidative stress appear to be different (6). While the hog1 mutant of H99 is hypersensitive to H2O2, the JEC21 hog1 mutant is resistant. In H99 but not in JEC21, the Hog1 MAPK cascade negatively regulates the mating processes and production of melanin and capsule. The mating ability and production of mating pheromone, capsule, and melanin are increased in the hog1 and pbs2 mutants of H99. In H99, fludioxonil treatment activates the Hog1 pathway and causes growth arrest, glycerol accumulation, and cell swelling. The hog1 and pbs2 mutants are resistant to fludioxonil (69). Hog1 is constitutively phosphorylated in H99 under normal conditions and rapidly dephosphorylated after exposure to 1 M NaCl. In JEC21 and a few other serotype D strains tested, like Hog1 in yeast, Hog1 in C. neoformans is rapidly phosphorylated in response to hyperosmotic stress. Nuclear localization of Hog1 is associated with its activation in H99 but less dependent on its phosphorylation in JEC21. The unique activation pattern of Hog1 is widespread in serotype A strains and in some clinical serotype D isolates, suggesting that C. neoformans may have adapted this pathway to control differentiation and virulence at the subspecies level, probably specific to environmental niches.

The hog1 and pbs2 mutants have attenuated virulence in infection assays with a murine cryptococcosis model. The pbs2 mutant is less virulent than the hog1 mutant, suggesting that Pbs2 has additional downstream targets that contribute to virulence. Similar to the hog1 and pbs2 mutants, deletion of a response regulator homologous to Ssk1 results in resistance to fludioxonil, enhanced mating efficiency, and increased sensitivity to various stresses (7). The ssk1 mutant also produces more melanin and capsule. However, the ssk1 mutant is less sensitive to hyperosmotic stress than the pbs2 and hog1 mutants. Although Ssk1 is required for Hog1 phosphorylation under normal conditions and in response to fludioxonil, Hog1 is still activated by high osmolarity in the ssk1 mutant. Therefore, Ssk1 is a major but not the only response regulator of the Pbs2-Hog1 pathway and is important but not essential for osmoregulation. A second response regulator is an Skn7 homolog, which governs resistance to oxidants and Na+ ions but may be not functionally related to the Hog1 pathway (150).

C. neoformans has seven putative histidine kinase genes (TCO1 to TCO7). One of them (TCO6) appears to be essential, but deletion of any other TCO genes individually does not cause hypersensitivity to high osmolarity or UV irradiation (7). Tco1 likely is a key sensor for negative regulation of melanin synthesis via the Hog1 pathway but has no effect on capsule production. Tco2 may play a role in Hog1 activation in response to oxidative stress. The tco2 mutant has increased sensitivity to oxidative stress but is less sensitive than the hog1 or pbs2 mutant. Tco2 also has overlapping functions with Tco1 in mediating fludioxonil sensitivity and Hog1 dephosphorylation in response to methylglyoxal (7). The tco1 tco2 double mutant but not the tco1 mutant or the tco2 mutant is as sensitive to hyperosmolarity as the hog1 mutant or the pbs2 mutant. Therefore, the Hog1 MAPK pathway may have multiple upstream sensors with shared and distinct functions.

In A. fumigatus, SakA and MpkC MAPKs both have the TGY phosphorylation motif, but they differ in functions. SakA is required for responses to heat shock, hyperosmotic, and oxidative stresses. It is also involved in the negative regulation of conidium germination under nitrogen- or carbon-deficient conditions (41, 155). In contrast, MpkC is dispensable for stress responses and conidium germination, but it may be involved in nutrient sensing, because the mpkC deletion mutant is defective in hyphal growth and conidium germination with sorbitol or mannitol as the sole carbon source. The expression pattern of mpkC also differs from that of sakA under various growth conditions, and only the sakA mutant is resistant to fludioxonil (66, 124). For putative upstream sensors, an Sln1 homolog, tcsB, and the OS-1 homolog fos-1 are dispensable for the response to hyperosmotic or oxidative stress (41, 120), but fos1 may play a role in cell wall assembly and conidiophore development.


arrow
CONCLUDING REMARKS
 
The Fus3/Kss1 homolog is more extensively studied than the other two MAPKs in fungal pathogens. In general, this well-conserved MAPK pathway is essential for regulating plant infection processes in phytopathogenic fungi, but it plays a lesser or no role in the virulence of human pathogens (Fig. 2). In the multihost pathogen F. oxysporum, the fmk1 mutant is nonpathogenic on plants but fully pathogenic in the murine model (113). In plant pathogens, this MAPK pathway may regulate the penetration of host physical barriers, such as cuticle and cell wall, which are not encountered by human pathogens. The Slt2 homologs also are essential for plant infection, but the functions of the HOG1 pathway vary among phytopathogenic fungi. In human pathogens, both the HOG1 and cell wall integrity pathways play important roles in virulence, probably for adaptation to physiological conditions and immune responses in the host. Interestingly, three classes of existing fungicides interfere with the HOG pathway in several fungi. Components of this pathway may be suitable as targets for developing new fungicides.


Figure 2
View larger version (22K):
[in this window]
[in a new window]

  		FIG. 2. MAPK pathways in fungal pathogens. The core components of three MAPK signal pathways in four selected fungal pathogens are in circles for Magnaporthe grisea, squares for Ustilago maydis, ovals for Candida albicans, and rectangles for Cryptococcus neoformans. Components that have been functionally characterized are in italic. The roles of these genes in fungal pathogenesis are shaded in black for essential, gray for important but not essential, and white for dispensable.

Although the MEKK-MEK-MAPK cascades are conserved, the upstream signal inputs and downstream transcription factors in pathogens are different from those of S. cerevisiae. Fungal pathogens may have novel receptors for sensing host and environmental signals to regulate penetration and infectious growth. Although Ras proteins have been shown to activate downstream MAPKs in several fungi, sequenced fungal genomes lack significant homologs of receptor kinase genes that function upstream from Ras in mammalian cells. Related to this subject, pathway specificity in fungal pathogens is not well studied. To date, no Ste5 homolog or Ste5-like scaffold protein in pathogenic fungi has been identified. With genomic resources becoming available for more and more fungi, comparative and functional genomic analyses will be useful to identify the missing regulatory and structural components of these MAPK pathways and their downstream targets or network of transcription factors.

Another interesting area is the interaction between the MAPK cascades and other signaling pathways. Several studies have indicated that cross talk occurs among MAPK pathways in fungal pathogens (42, 43, 69). However, the exact molecular mechanisms regulating their interaction are not clear, and the relationship between these pathways during infection may be more complex than what has been observed in in vitro cultures. MAPKs are also known to interact with the cAMP signaling in pathogenesis, differentiation, and stress response in U. maydis, C. neoformans, and other fungi (40, 79). Further characterization of these signal transduction pathways and their interaction in various fungal pathogens is necessary for a better understanding of fungal development and pathogenesis.


arrow
ACKNOWLEDGMENTS
 
We thank Paul Tudzynski, Youliang Peng, and Antonio Di Pietro for communicating unpublished results. We also thank Larry Dunkle and Stephen Goodwin for critical reading of the manuscript.

This is journal article no. 18184 of the Purdue University Agricultural Experiment Station.


arrow
FOOTNOTES
 
* Corresponding author. Mailing address: Department of Botany and Plant Pathology, Purdue University, West Lafayette, IN 47907. Phone: (765) 496-6918. Fax: (765) 496-6918. E-mail: jinrong{at}purdue.edu Back

{triangledown} Published ahead of print on 22 August 2007. Back


arrow
REFERENCES
 
    1
  1. Alonso-Monge, R., F. Navarro-Garcia, E. Roman, A. I. Negredo, B. Eisman, U. Nombela, and J. Pla. 2003. The Hog1 mitogen-activated protein kinase is essential in the oxidative stress response and chlamydospore formation in Candida albicans. Eukaryot. Cell 2:351-361.[Abstract/Free Full Text]
    2. 2
  2. Alonso-Monge, R., E. Roman, C. Nombela, and J. Pla. 2006. The MAP kinase signal transduction network in Candida albicans. Microbiology 152:905-912.[Abstract/Free Full Text]
    3. 3
  3. Alspaugh, J. A., L. M. Cavallo, J. R. Perfect, and J. Heitman. 2000. RAS1 regulates filamentation, mating and growth at high temperature of Cryptococcus neoformans. Mol. Microbiol. 36:352-365.[CrossRef][Medline]
    4. 4
  4. Alspaugh, J. A., J. R. Perfect, and J. Heitman. 1997. Cryptococcus neoformans mating and virulence are regulated by the G-protein alpha subunit GPA1 and cAMP. Genes Dev. 11:3206-3217.[Abstract/Free Full Text]
    5. 5
  5. Arana, D. M., C. Nombela, R. Alonso-Monge, and J. Pla. 2005. The Pbs2 MAP kinase kinase is essential for the oxidative-stress response in the fungal pathogen Candida albicans. Microbiology 151:1033-1049.[Abstract/Free Full Text]
    6. 6
  6. Bahn, Y. S., K. Kojima, G. M. Cox, and J. Heitman. 2005. Specialization of the HOG pathway and its impact on differentiation and virulence of Cryptococcus neoformans. Mol. Biol. Cell 16:2285-2300.[Abstract/Free Full Text]
    7. 7
  7. Bahn, Y. S., K. Kojima, G. M. Cox, and J. Heitman. 2006. A unique fungal two-component system regulates stress responses, drug sensitivity, sexual development, and virulence of Cryptococcus neoformans. Mol. Biol. Cell 17:3122-3135.[Abstract/Free Full Text]
    8. 8
  8. Banno, S., R. Noguchi, K. Yamashita, F. Fukumori, M. Kimura, I. Yamaguchi, and M. Fujimura. 2007. Roles of putative His-to-Asp signaling modules HPT-1 and RRG-2, on viability and sensitivity to osmotic and oxidative stresses in Neurospora crassa. Curr. Genet. 51:197-208.[CrossRef][Medline]
    9. 9
  9. Bardwell, L. 2004. A walk-through of the yeast mating pheromone response pathway. Peptides 25:1465-1476.[CrossRef][Medline]
    10. 10
  10. Basse, C. W., and G. Steinberg. 2004. Ustilago maydis, model system for analysis of the molecular basis of fungal pathogenicity. Mol. Plant Pathol. 5:83-92.[CrossRef]
    11. 11
  11. Bennett, R. J., and A. D. Johnson. 2005. Mating in Candida albicans and the search for a sexual cycle. Annu. Rev. Microbiol. 59:233-255.[CrossRef][Medline]
    12. 12
  12. Bhattacharyya, R. P., A. Remenyi, M. C. Good, C. J. Bashor, A. M. Falick, and W. A. Lim. 2006. The Ste5 scaffold allosterically modulates signaling output of the yeast mating pathway. Science 311:822-826.[Abstract/Free Full Text]
    13. 13
  13. Biswas, K., and J. Morschhauser. 2005. The Mep2p ammonium permease controls nitrogen starvation-induced filamentous growth in Candida albicans. Mol. Microbiol. 56:649-669.[CrossRef][Medline]
    14. 14
  14. Borneman, A. R., M. J. Hynes, and A. Andrianopoulos. 2001. An STE12 homolog from the asexual, dimorphic fungus Penicillium marneffei complements the defect in sexual development of an Aspergillus nidulans steA mutant. Genetics 157:1003-1014.[Abstract/Free Full Text]
    15. 15
  15. Brachmann, A., J. Schirawski, P. Muller, and R. Kahmann. 2003. An unusual MAP kinase is required for efficient penetration of the plant surface by Ustilago maydis. EMBO J. 22:2199-2210.[CrossRef][Medline]
    16. 16
  16. Braun, B. R., and A. D. Johnson. 2000. TUP1, CPH1 and EFG1 make independent contributions to filamentation in Candida albicans. Genetics 155:57-67.[Abstract/Free Full Text]
    17. 17
  17. Brefort, T., P. Muller, and R. Kahmann. 2005. The high-mobility-group domain transcription factor Rop1 is a direct regulator of prf1 in Ustilago maydis. Eukaryot. Cell 4:379-391.[Abstract/Free Full Text]
    18. 18
  18. Bruno, K. S., F. Tenjo, L. Li, J. E. Hamer, and J. R. Xu. 2004. Cellular localization and role of kinase activity of PMK1 in Magnaporthe grisea. Eukaryot. Cell 3:1525-1532.[Abstract/Free Full Text]
    19. 19
  19. Bussink, H. J., and S. A. Osmani. 1999. A mitogen-activated protein kinase (MPKA) is involved in polarized growth in the filamentous fungus Aspergillus nidulans. FEMS Microbiol. Lett. 173:117-125.[Medline]
    20. 20
  20. Chang, Y. C., G. F. Miller, and K. J. Kwon-Chung. 2003. Importance of a developmentally regulated pheromone receptor of Cryptococcus neoformans for virulence. Infect. Immun. 71:4953-4960.[Abstract/Free Full Text]
    21. 21
  21. Chang, Y. C., and L. A. Penoyer. 2000. Properties of various RHO1 mutant alleles of Cryptococcus neoformans. J. Bacteriol. 182:4987-4991.[Abstract/Free Full Text]
    22. 22
  22. Chang, Y. C., B. L. Wickes, G. F. Miller, L. A. Penoyer, and K. J. Kwon-Chung. 2000. Cryptococcus neoformans STE12 alpha regulates virulence but is not essential for mating. J. Exp. Med. 191:871-881.[Abstract/Free Full Text]
    23. 23
  23. Chauhan, N., D. Inglis, E. Roman, J. Pla, D. Li, J. A. Calera, and R. Calderone. 2003. Candida albicans response regulator gene SSK1 regulates a subset of genes whose functions are associated with cell wall biosynthesis and adaptation to oxidative stress. Eukaryot. Cell 2:1018-1024.[Abstract/Free Full Text]
    24. 24
  24. Chen, C. B., A. Harel, R. Gorovoits, O. Yarden, and M. B. Dickman. 2004. MAPK regulation of sclerotial development in Sclerotinia sclerotiorum is linked with pH and cAMP sensing. Mol. Plant-Microbe Interact. 17:404-413.[Medline]
    25. 25
  25. Chen, J. Y., J. Chen, S. Lane, and H. P. Liu. 2002. A conserved mitogen-activated protein kinase pathway is required for mating in Candida albicans. Mol. Microbiol. 46:1335-1344.[CrossRef][Medline]
    26. 26
  26. Cho, Y., R. A. Cramer, K. Kim, J. Davis, T. K. Mitchell, P. Figuli, B. A. Pryor, E. Lemasters, and C. B. Lawrence. 2007. The Fus3/Kss1 MAP kinase homolog Amk1 regulates the expression of genes encoding hydrolytic enzymes in Alternaria brassicicola. Fungal Genet. Biol. 44:543-553.[CrossRef][Medline]
    27. 27
  27. Choi, E. S., H. J. Chung, M. J. Kim, S. M. Park, B. J. Cha, M. S. Yang, and D. H. Kim. 2005. Characterization of the ERK homologue CpMK2 from the chestnut blight fungus Cryphonectria parasitica. Microbiology 151:1349-1358.[Abstract/Free Full Text]
    28. 28
  28. Chou, S., S. Lane, and H. P. Liu. 2006. Regulation of mating and filamentation genes by two distinct Ste12 complexes in Saccharomyces cerevisiae. Mol. Cell. Biol. 26:4794-4805.[Abstract/Free Full Text]
    29. 29
  29. Clarke, D. L., G. L. Woodlee, C. M. McClelland, T. S. Seymour, and B. L. Wickes. 2001. The Cryptococcus neoformans STE11 alpha gene is similar to other fungal mitogen-activated protein kinase kinase kinase (MAPKKK) genes but is mating type specific. Mol. Microbiol. 40:200-213.[CrossRef][Medline]
    30. 30
  30. Cousin, A., R. Mehrabi, M. Guilleroux, M. Dufresne, T. Van der Lee, C. Waalwijk, T. Langin, and G. H. J. Kema. 2006. The MAP kinase-encoding gene MgFus3 of the non-appressorium phytopathogen Mycosphaerella graminicola is required for penetration and in vitro pycnidia formation. Mol. Plant Pathol. 7:269-278.[CrossRef]
    31. 31
  31. Davidson, R. C., C. B. Nichols, G. M. Cox, J. R. Perfect, and J. Heitman. 2003. A MAP kinase cascade composed of cell type specific and non-specific elements controls mating and differentiation of the fungal pathogen Cryptococcus neoformans. Mol. Microbiol. 49:469-485.[CrossRef][Medline]
    32. 32
  32. Dean, R. A., N. J. Talbot, D. J. Ebbole, M. Farman, et al. 2005. The genome sequence of the rice blast fungus Magnaporthe grisea. Nature 434:980-986.[CrossRef][Medline]
    33. 33
  33. Delgado-Jarana, J. S., A. L. Martinez-Rocha, R. Roldan-Rodriguez, M. I. G. Roncero, and A. Di Pietro. 2005. Fusarium oxysporum G-protein beta subunit Fgb1 regulates hyphal growth, development, and virulence through multiple signaling pathways. Fungal Genet. Biol. 42:61-72.[CrossRef][Medline]
    34. 34
  34. Deng, F. Y., T. D. Allen, and D. L. Nuss. 2007. Ste12 transcription factor homologue CpST12 is down-regulated by hypovirus infection and required for virulence and female fertility of the chestnut blight fungus Cryphonectria parasitica. Eukaryot. Cell 6:235-244.[Abstract/Free Full Text]
    35. 35
  35. DeZwaan, T. M., A. M. Carroll, B. Valent, and J. A. Sweigard. 1999. Magnaporthe grisea Pth11p is a novel plasma membrane protein that mediates appressorium differentiation in response to inductive substrate cues. Plant Cell 11:2013-2030.[Abstract/Free Full Text]
    36. 36
  36. Diez-Orejas, R., G. Molero, F. Navarro-Garcia, J. Pla, C. Nombela, and M. Sanchez-Perez. 1997. Reduced virulence of Candida albicans MKC1 mutants: a role for mitogen-activated protein kinase in pathogenesis. Infect. Immun. 65:833-837.[Abstract]
    37. 37
  37. Di Pietro, A., F. I. Garcia-Maceira, E. Meglecz, and M. I. G. Roncero. 2001. A MAP kinase of the vascular wilt fungus Fusarium oxysporum is essential for root penetration and pathogenesis. Mol. Microbiol. 39:1140-1152.[CrossRef][Medline]
    38. 38
  38. Dixon, K. P., J. R. Xu, N. Smirnoff, and N. J. Talbot. 1999. Independent signaling pathways regulate cellular turgor during hyperosmotic stress and appressorium-mediated plant infection by Magnaporthe grisea. Plant Cell 11:2045-2058.[Abstract/Free Full Text]
    39. 39
  39. Doehlemann, G., P. Berndt, and M. Hahn. 2006. Different signalling pathways involving a G alpha protein, cAMP and a MAP kinase control germination of Botrytis cinerea conidia. Mol. Microbiol. 59:821-835.[CrossRef][Medline]
    40. 40
  40. D'Souza, C. A., and J. Heitman. 2001. Conserved cAMP signaling cascades regulate fungal development and virulence. FEMS Microbiol. Rev. 25:349-364.[CrossRef][Medline]
    41. 41
  41. Du, C., J. Sarfati, J. P. Latge, and R. Calderone. 2006. The role of the sakA (Hog1) and tcsB (S1n1) genes in the oxidant adaptation of Aspergillus fumigatus. Med. Mycol. 44:211-218.[CrossRef][Medline]
    42. 42
  42. Eisman, B., R. Alonso-Monge, E. Roman, D. Arana, C. Nombela, and J. Pla. 2006. The Cek1 and Hog1 mitogen-activated protein kinases play complementary roles in cell wall biogenesis and chlamydospore formation in the fungal pathogen Candida albicans. Eukaryot. Cell 5:347-358.[Abstract/Free Full Text]
    43. 43
  43. Eliahu, N., A. Igbaria, M. S. Rose, B. A. Horwitz, and S. Lev. 2007. Melanin biosynthesis in the maize pathogen Cochliobolus heterostrophus depends on two mitogen-activated protein kinases, Chk1 and Mps1, and the transcription factor Cmr1. Eukaryot. Cell 6:421-429.[Abstract/Free Full Text]
    44. 44
  44. Fernandes, L., M. A. M. Araújo, A. Amaral, et al. 2005. Cell signaling pathways in Paracoccidioides brasiliensis—inferred from comparisons with other fungi. Genet. Mol. Res. 4:216-231.[Medline]
    45. 45
  45. Fox, D., and A. G. Smulian. 1999. Mitogen-activated protein kinase Mkp1 of Pneumocystis carinii complements the slt2 defect in the cell integrity pathway of Saccharomyces cerevisiae. Mol. Microbiol. 34:451-462.[CrossRef][Medline]
    46. 46
  46. Furukawa, K., Y. Hoshi, T. Maeda, T. Nakajima, and K. Abe. 2005. Aspergillus nidulans HOG pathway is activated only by two-component signalling pathway in response to osmotic stress. Mol. Microbiol. 56:1246-1261.[CrossRef][Medline]
    47. 47
  47. Ganem, S., S. W. Lu, B. Lee, D. Chou, R. Hadar, B. G. Turgeon, and B. A. Horwitz. 2004. G-protein beta subunit of Cochliobolus heterostrophus involved in virulence, asexual and sexual reproductive ability, and morphogenesis. Eukaryot. Cell 3:1653-1663.[Abstract/Free Full Text]
    48. 48
  48. Garrido, E., U. Voss, P. Muller, S. Castillo-Lluva, R. Kahmann, and J. Perez-Martin. 2004. The induction of sexual development and virulence in the smut fungus Ustilago maydis depends on Crk1, a novel MAPK protein. Genes Dev. 18:3117-3130.[Abstract/Free Full Text]
    49. 49
  49. Gerik, K. J., M. J. Donlin, C. E. Soto, A. M. Banks, I. R. Banks, M. A. Maligie, C. P. Selitrennikoff, and J. K. Lodge. 2005. Cell wall integrity is dependent on the PKC1 signal transduction pathway in Cryptococcus neoformans. Mol. Microbiol. 58:393-408.[CrossRef][Medline]
    50. 50
  50. Gustin, M. C., J. Albertyn, M. Alexander, and K. Davenport. 1998. MAP kinase pathways in the yeast Saccharomyces cerevisiae. Microbiol. Mol. Biol. Rev. 62:1264-1300.[Abstract/Free Full Text]
    51. 51
  51. Han, K. H., and R. A. Prade. 2002. Osmotic stress-coupled maintenance of polar growth in Aspergillus nidulans. Mol. Microbiol. 43:1065-1078.[CrossRef][Medline]
    52. 52
  52. Heinisch, J. J. 2005. Baker's yeast as a tool for the development of antifungal kinase inhibitors—targeting protein kinase C and the cell integrity pathway. Biochim. Biophys. Acta 1754:171-182.[Medline]
    53. 53
  53. Heung, L. J., C. Luberto, A. Plowden, Y. A. Hannun, and M. Del Poeta. 2004. The sphingolipid pathway regulates Pkc1 through the formation of diacylglycerol in Cryptococcus neoformans. J. Biol. Chem. 279:21144-21153.[Abstract/Free Full Text]
    54. 54
  54. Hohmann, S. 2002. Osmotic stress signaling and osmoadaptation in yeasts. Microbiol. Mol. Biol. Rev. 66:300-372.[Abstract/Free Full Text]
    55. 55
  55. Hou, Z., C. Xue, Y. Peng, T. Katan, H. C. Kistler, and J. R. Xu. 2002. A mitogen-activated protein kinase gene (MGV1) in Fusarium graminearum is required for female fertility, heterokaryon formation, and plant infection. Mol. Plant-Microbe Interact. 15:1119-1127.[Medline]
    56. 56
  56. Hu, G., A. Kamp, R. Linning, S. Naik, and G. Bakkeren. 2007. Complementation of Ustilago maydis MAPK mutants by a wheat leaf rust, Puccinia triticina homolog: potential for functional analyses of rust genes. Mol. Plant-Microbe Interact. 20:637-647.[CrossRef][Medline]
    57. 57
  57. Jenczmionka, N. J., F. J. Maier, A. P. Losch, and W. Schafer. 2003. Mating, conidiation and pathogenicity of Fusarium graminearum, the main causal agent of the head-blight disease of wheat, are regulated by the MAP kinase gpmk1. Curr. Genet. 43:87-95.[Medline]
    58. 58
  58. Jenczmionka, N. J., and W. Schafer. 2005. The Gpmk1 MAP kinase of Fusarium graminearum regulates the induction of specific secreted enzymes. Curr. Genet. 47:29-36.[CrossRef][Medline]
    59. 59
  59. Jones, C. A., S. E. Greer-Phillips, and K. A. Borkovich. 2007. The response regulator RRG-1 functions upstream of a mitogen-activated protein kinase pathway impacting asexual development, female fertility, osmotic stress, and fungicide resistance in Neurospora crassa. Mol. Biol. Cell 18:2123-2136.[Abstract/Free Full Text]
    60. 60
  60. Jung, U. S., A. K. Sobering, M. J. Romeo, and D. E. Levin. 2002. Regulation of the yeast Rlm1 transcription factor by the Mpk1 cell wall integrity MAP kinase. Mol. Microbiol. 46:781-789.[CrossRef][Medline]
    61. 61
  61. Kadosh, D., and A. D. Johnson. 2005. Induction of the Candida albicans filamentous growth program by relief of transcriptional repression: a genome-wide analysis. Mol. Biol. Cell 16:2903-2912.[Abstract/Free Full Text]
    62. 62
  62. Kaffarnik, F., P. Muller, M. Leibundgut, R. Kahmann, and M. Feldbrugge. 2003. PKA and MAPK phosphorylation of Prf1 allows promoter discrimination in Ustilago maydis. EMBO J. 22:5817-5826.[CrossRef][Medline]
    63. 63
  63. Kahmann, R., and J. Kamper. 2004. Ustilago maydis: how its biology relates to pathogenic development. New Phytol. 164:31-42.[CrossRef]
    64. 64
  64. Kawasaki, L., O. Sanchez, K. Shiozaki, and J. Aguirre. 2002. SakA MAP kinase is involved in stress signal transduction, sexual development and spore viability in Aspergillus nidulans. Mol. Microbiol. 45:1153-1163.[CrossRef][Medline]
    65. 65
  65. Kicka, S., C. Bonnet, A. K. Sobering, L. P. Ganesan, and P. Silar. 2006. A mitotically inheritable unit containing a MAP kinase module. Proc. Natl. Acad. Sci. USA 103:13445-13450.[Abstract/Free Full Text]
    66. 66
  66. Kim, J. H., B. C. Campbell, N. Mahoney, K. L. Chan, and G. S. May. 2006. Targeting antioxidative signal transduction and stress response system: control of pathogenic Aspergillus with phenolics that inhibit mitochondrial function. J. Appl. Microbiol. 101:181-189.[CrossRef][Medline]
    67. 67
  67. Kinane, J., and R. P. Oliver. 2003. Evidence that the appressorial development in barley powdery mildew is controlled by MAP kinase activity in conjunction with the cAMP pathway. Fungal Genet. Biol. 39:94-102.[CrossRef][Medline]
    68. 68
  68. Klose, J., M. M. de Sa, and J. W. Kronstad. 2004. Lipid-induced filamentous growth in Ustilago maydis. Mol. Microbiol. 52:823-835.[CrossRef][Medline]
    69. 69
  69. Kojima, K., Y. S. Bahn, and J. Heitman. 2006. Calcineurin, Mpk1 and Hog1 MAPK pathways independently control fludioxonil antifungal sensitivity in Cryptococcus neoformans. Microbiology 152:591-604.[Abstract/Free Full Text]
    70. 70
  70. Kojima, K., T. Kikuchi, Y. Takano, E. Oshiro, and T. Okuno. 2002. The mitogen-activated protein kinase gene MAF1 is essential for the early differentiation phase of appressorium formation in Colletotrichum lagenarium. Mol. Plant-Microbe Interact. 15:1268-1276.[Medline]
    71. 71
  71. Kojima, K., Y. Takano, A. Yoshimi, C. Tanaka, T. Kikuchi, and T. Okuno. 2004. Fungicide activity through activation of a fungal signaling pathway. Mol. Microbiol. 53:1785-1796.[CrossRef][Medline]
    72. 72
  72. Kothe, G. O., and S. J. Free. 1998. The isolation and characterization of NRC-1 and NRC-2, two genes encoding protein kinases that control growth and development in Neurospora crassa. Genetics 149:117-130.[Abstract/Free Full Text]
    73. 73
  73. Kraus, P. R., D. S. Fox, G. M. Cox, and J. Heitman. 2003. The Cryptococcus neoformans MAP kinase Mpk1 regulates cell integrity in response to antifungal drugs and loss of calcineurin function. Mol. Microbiol. 48:1377-1387.[CrossRef][Medline]
    74. 74
  74. Kruppa, M., and R. Calderone. 2006. Two-component signal transduction in human fungal pathogens. FEMS Yeast Res. 6:149-159.[CrossRef][Medline]
    75. 75
  75. Kulkarni, R. D., M. R. Thon, H. Q. Pan, and R. A. Dean. 2005. Novel G-protein-coupled receptor-like proteins in the plant pathogenic fungus Magnaporthe grisea. Genome Biol. 6:R24.[CrossRef][Medline]
    76. 76
  76. Kumamoto, C. A. 2005. A contact-activated kinase signals Candida albicans invasive growth and biofilm development. Proc. Natl. Acad. Sci. USA 102:5576-5581.[Abstract/Free Full Text]
    77. 77
  77. Lane, S., C. Birse, S. Zhou, R. Matson, and H. P. Liu. 2001. DNA array studies demonstrate convergent regulation of virulence factors by Cph1, Cph2, and Efg1 in Candida albicans. J. Biol. Chem. 276:48988-48996.[Abstract/Free Full Text]
    78. 78
  78. Leberer, E., D. Harcus, D. Dignard, L. Johnson, S. Ushinsky, D. Y. Thomas, and K. Schroppel. 2001. Ras links cellular morphogenesis to virulence by regulation of the MAP kinase and cAMP signalling pathways in the pathogenic fungus Candida albicans. Mol. Microbiol. 42:673-687.[CrossRef][Medline]
    79. 79
  79. Lee, N., C. A. D'Souza, and J. W. Kronstad. 2003. Of smuts, blasts, mildews, and blights: cAMP signaling in phytopathogenic fungi. Annu. Rev. Phytopathol. 41:399-427.[CrossRef][Medline]
    80. 80
  80. Lee, N., and J. W. Kronstad. 2002. ras2 controls morphogenesis, pheromone response, and pathogenicity in the fungal pathogen Ustilago maydis. Eukaryot. Cell 1:954-966.[Abstract/Free Full Text]
    81. 81
  81. Lengeler, K. B., R. C. Davidson, C. A. D'Souza, T. Harashima, W. Shen, P. Wang, X. W. Pan, M. S. Waugh, and J. Heitman. 2000. Signal transduction cascades regulating fungal development and virulence. Microbiol. Mol. Biol. Rev. 64:746-785.[Abstract/Free Full Text]
    82. 82
  82. Lev, S., and B. A. Horwitz. 2003. A mitogen-activated protein kinase pathway modulates the expression of two cellulase genes in Cochliobolus heterostrophus during plant infection. Plant Cell 15:835-844.[Abstract/Free Full Text]
    83. 83
  83. Lev, S., A. Sharon, R. Hadar, H. Ma, and A. Horwitz Benjamin. 1999. A mitogen-activated protein kinase of the corn leaf pathogen Cochliobolus heterostrophus is involved in conidiation, appressorium formation, and pathogenicity: diverse roles for mitogen-activated protein kinase homologs in foliar pathogens. Proc. Natl. Acad. Sci. USA 96:13542-13547.[Abstract/Free Full Text]
    84. 84
  84. Li, D., P. Bobrowicz, H. H. Wilkinson, and D. J. Ebbole. 2005. A mitogen-activated protein kinase pathway essential for mating and contributing to vegetative growth in Neurospora crassa. Genetics 170:1091-1104.[Abstract/Free Full Text]
    85. 85
  85. Li, L., C. Y. Xue, K. Bruno, M. Nishimura, and J. R. Xu. 2004. Two PAK kinase genes, CHM1 and MST20, have distinct functions in Magnaporthe grisea. Mol. Plant-Microbe Interact. 17:547-556.[Medline]
    86. 86
  86. Liu, H., A. Suresh, F. S. Willard, D. P. Siderovski, S. Lu, and N. I. Naqvi. 2007. Rgs1 regulates multiple G alpha subunits in Magnaporthe pathogenesis, asexual growth and thigmotropism. EMBO J. 26:690-700.[CrossRef][Medline]
    87. 87
  87. Liu, S., and R. A. Dean. 1997. G protein alpha subunit genes control growth, development, and pathogenicity of Magnaporthe grisea. Mol. Plant-Microbe Interact. 10:1075-1086.[Medline]
    88. 88
  88. Lo, H. J., J. R. Kohler, B. DiDomenico, D. Loebenberg, A. Cacciapuoti, and G. R. Fink. 1997. Nonfilamentous C. albicans mutants are avirulent. Cell 90:939-949.[CrossRef][Medline]
    89. 89
  89. Marques, J. M., R. J. Rodrigues, A. C. de Magalhaes-Sant'Ana, and T. Goncalves. 2006. Saccharomyces cerevisiae Hog1 protein phosphorylation upon exposure to bacterial endotoxin. J. Biol. Chem. 281:24687-24694.[Abstract/Free Full Text]
    90. 90
  90. Martinez-Espinoza, A. D., J. Ruiz-Herrera, C. G. Leon-Ramirez, and S. E. Gold. 2004. MAP kinase and CAMP signaling pathways modulate the pH-induced yeast-to-mycelium dimorphic transition in the corn smut fungus Ustilago maydis. Curr. Microbiol. 49:274-281.[CrossRef][Medline]
    91. 91
  91. Mayorga, M. E., and S. E. Gold. 2001. The ubc2 gene of Ustilago maydis encodes a putative novel adaptor protein required for filamentous growth, pheromone response and virulence. Mol. Microbiol. 41:1365-1379.[CrossRef][Medline]
    92. 92
  92. Mehrabi, R., T. van der Lee, C. Waalwijk, and G. H. J. Kema. 2006. MgSlt2, a cellular integrity MAP kinase gene of the fungal wheat pathogen Mycosphaerella graminicola, is dispensable for penetration but essential for invasive growth. Mol. Plant-Microbe Interact. 19:389-398.[Medline]
    93. 93
  93. Mehrabi, R., L.-H. Zwiers, M. A. de Waard, and G. H. J. Kema. 2006. MgHog1 regulates dimorphism and pathogenicity in the fungal wheat pathogen Mycosphaerella graminicola. Mol. Plant-Microbe Interact. 19:1262-1269.[CrossRef][Medline]
    94. 94
  94. Menon, V., D. M. Li, N. Chauhan, R. Rajnarayanan, A. Dubrovska, A. H. West, and R. Calderone. 2006. Functional studies of the Ssk1p response regulator protein of Candida albicans as determined by phenotypic analysis of receiver domain point mutants. Mol. Microbiol. 62:997-1013.[CrossRef][Medline]
    95. 95
  95. Menotta, M., R. Pierleoni, A. Amicucci, D. Sisti, A. Cerasi, E. Millo, L. Chiarantini, and V. Stocchi. 2006. Characterization and complementation of a Fus3/Kss1 type MAPK from Tuber borchii, TBMK. Mol. Genet. Genomics 276:126-134.[CrossRef][Medline]
    96. 96
  96. Mey, G., K. Held, J. Scheffer, K. B. Tenberge, and P. Tudzynski. 2002. CPMK2, an SLT2-homologous mitogen-activated protein (MAP) kinase, is essential for pathogenesis of Claviceps purpurea on rye: evidence for a second conserved pathogenesis-related MAP kinase cascade in phytopathogenic fungi. Mol. Microbiol. 46:305-318.[CrossRef][Medline]
    97. 97
  97. Mey, G., B. Oeser, M. H. Lebrun, and P. Tudzynski. 2002. The biotrophic, non-appressorium-forming grass pathogen Claviceps purpurea needs a Fus3/Pmk1 homologous mitogen-activated protein kinase for colonization of rye ovarian tissue. Mol. Plant-Microbe Interact. 15:303-312.[Medline]
    98. 98
  98. Miller, M. G., and A. D. Johnson. 2002. White-opaque switching in Candida albicans is controlled by mating-type locus homeodomain proteins and allows efficient mating. Cell 110:293-302.[CrossRef][Medline]
    99. 99
  99. Molero, G., M. V. Guillen, L. Martinez-Solano, C. Gil, J. Pla, C. Nombela, M. Sanchez-Perez, and R. Diez-Orejas. 2005. The importance of the phagocytes' innate response in resolution of the infection induced by a low virulent Candida albicans mutant. Scand. J. Immunol. 62:224-233.[CrossRef][Medline]
    100. 100
  100. Mollapour, M., and P. W. Piper. 2006. Hog1p mitogen-activated protein kinase determines acetic acid resistance in Saccharomyces cerevisiae. FEMS Yeast Res. 6:1274-1280.[CrossRef][Medline]
    101. 101
  101. Moriwaki, A., J. Kihara, C. Mori, and S. Arase. 2007. A MAP kinase gene, BMK1, is required for conidiation and pathogenicity in the rice leaf spot pathogen Bipolaris oryzae. Microbiol. Res. 162:108-114.[CrossRef][Medline]
    102. 102
  102. Moriwaki, A., E. Kubo, S. Arase, and J. Kihara. 2006. Disruption of SRM1, a mitogen-activated protein kinase gene, affects sensitivity to osmotic and ultraviolet stressors in the phytopathogenic fungus Bipolaris oryzae. FEMS Microbiol. Lett. 257:253-261.[CrossRef][Medline]
    103. 103
  103. Motoyama, T., K. Kadokura, T. Ohira, A. Ichiishi, M. Fujimura, I. Yamaguchi, and T. Kudo. 2005. A two-component histidine kinase of the rice blast fungus is involved in osmotic stress response and fungicide action. Fungal Genet. Biol. 42:200-212.[CrossRef][Medline]
    104. 104
  104. Muller, P., J. D. Katzenberger, G. Loubradou, and R. Kahmann. 2003. Guanyl nucleotide exchange factor Sql2 and Ras2 regulate filamentous growth in Ustilago maydis. Eukaryot. Cell 2:609-617.[Abstract/Free Full Text]
    105. 105
  105. Muller, P., A. Leibbrandt, H. Teunissen, S. Cubasch, C. Aichinger, and R. Kahmann. 2004. The Gß-subunit-encoding gene bpp1 controls cyclic-AMP signaling in Ustilago maydis. Eukaryot. Cell 3:806-814.[Abstract/Free Full Text]
    106. 106
  106. Muller, P., G. Weinzierl, A. Brachmann, M. Feldbrugge, and R. Kahmann. 2003. Mating and pathogenic development of the smut fungus Ustilago maydis are regulated by one mitogen-activated protein kinase cascade. Eukaryot. Cell 2:1187-1199.[Abstract/Free Full Text]
    107. 107
  107. Navarro-Garcia, F., R. Alonso-Monge, H. Rico, J. Pla, R. Sentandreu, and C. Nombela. 1998. A role for the MAP kinase gene MKC1 in cell wall construction and morphological transitions in Candida albicans. Microbiology 144:411-424.[Abstract/Free Full Text]
    108. 108
  108. Navarro-Garcia, F., B. Eisman, S. M. Fiuza, C. Nombela, and J. Pla. 2005. The MAP kinase Mkc1p is activated under different stress conditions in Candida albicans. Microbiology 151:2737-2749.[Abstract/Free Full Text]
    109. 109
  109. Navarro-Garcia, F., M. Sanchez, J. Pla, and C. Nombela. 1995. Functional characterization of the MKC1 gene of Candida albicans, which encodes a mitogen-activated protein-kinase homolog related to cell integrity. Mol. Cell. Biol. 15:2197-2206.[Abstract]
    110. 110
  110. Nishimura, M., G. Park, and J. R. Xu. 2003. The G-beta subunit MGB1 is involved in regulating multiple steps of infection-related morphogenesis in Magnaporthe grisea. Mol. Microbiol. 50:231-243.[CrossRef][Medline]
    111. 111
  111. Noguchi, R., S. Banno, R. Ichikawa, F. Fukumori, A. Ichiishi, M. Kimura, I. Yamaguchi, and M. Fujimura. 2007. Identification of OS-2 MAP kinase-dependent genes induced in response to osmotic stress, antifungal agent fludioxonil, and heat shock in Neurospora crassa. Fungal Genet. Biol. 44:208-218.[CrossRef][Medline]
    112. 112
  112. O'Rourke, S. M., and I. Herskowitz. 2002. A third osmosensing branch in Saccharomyces cerevisiae requires the Msb2 protein and functions in parallel with the Sho1 branch. Mol. Cell. Biol. 22:4739-4749.[Abstract/Free Full Text]
    113. 113
  113. Ortoneda, M., J. Guarro, M. P. Madrid, Z. Caracuel, M. I. G. Roncero, E. Mayayo, and A. Di Pietro. 2004. Fusarium oxysporum as a multihost model for the genetic dissection of fungal virulence in plants and mammals. Infect. Immun. 72:1760-1766.[Abstract/Free Full Text]
    114. 114
  114. Pan, X. W., and J. Heitman. 2002. Protein kinase A operates a molecular switch that governs yeast pseudohyphal differentiation. Mol. Cell. Biol. 22:3981-3993.[Abstract/Free Full Text]
    115. 115
  115. Panadero, J., C. Pallotti, S. Rodriguez-Vargas, F. Randez-Gil, and J. A. Prieto. 2006. A downshift in temperature activates the high osmolarity glycerol (HOG) pathway, which determines freeze tolerance in Saccharomyces cerevisiae. J. Biol. Chem. 281:4638-4645.[Abstract/Free Full Text]
    116. 116
  116. Pandey, A., M. G. Roca, N. D. Read, and N. L. Glass. 2004. Role of mitogen-activated protein kinase pathway during conidial germination and hyphal fusion in Neurospora crassa. Eukaryot. Cell 3:348-358.[Abstract/Free Full Text]
    117. 117
  117. Park, G., K. S. Bruno, C. J. Staiger, N. J. Talbot, and J. R. Xu. 2004. Independent genetic mechanisms mediate turgor generation and penetration peg formation during plant infection in the rice blast fungus. Mol. Microbiol. 53:1695-1707.[CrossRef][Medline]
    118. 118
  118. Park, G., C. Xue, X. Zhao, Y. Kim, M. Orbach, and J. R. Xu. 2006. Multiple upstream signals converge on an adaptor protein Mst50 to activate the PMK1 pathway in Magnaporthe grisea. Plant Cell 18:2822-2835.[Abstract/Free Full Text]
    119. 119
  119. Park, S. H., E. S. Choi, M. J. Kim, B. J. Cha, M. S. Yang, and D. H. Kim. 2004. Characterization of HOG1 homologue, CpMK1, from Cryphonectria parasitica and evidence for hypovirus-mediated perturbation of its phosphorylation in response to hypertonic stress. Mol. Microbiol. 51:1267-1277.[CrossRef][Medline]
    120. 120
  120. Pott, G. B., T. K. Miller, J. A. Bartlett, J. S. Palas, and C. P. Selitrennikoff. 2000. The isolation of FOS-1, a gene encoding a putative two-component histidine kinase from Aspergillus fumigatus. Fungal Genet. Biol. 31:55-67.[CrossRef][Medline]
    121. 121
  121. Prados-Rosales, R. C., C. Serena, J. Delgado-Jarana, J. Guarro, and A. Di Pietro. 2006. Distinct signalling pathways coordinately contribute to virulence of Fusarium oxysporum on mammalian hosts. Microbes Infect. 8:2825-2831.[CrossRef][Medline]
    122. 122
  122. Ramamoorthy, V., X. Zhao, A. Snyder, J. R. Xu, and D. M. Shah. 2007. Two mitogen-activated protein kinase signalling cascades mediate basal resistance to antifungal plant defensins in Fusarium graminearum. Cell. Microbiol. 9:1491-1506.[CrossRef][Medline]
    123. 123
  123. Rauyaree, P., M. D. Ospina-Giraldo, S. Kang, R. G. Bhat, K. V. Subbarao, S. J. Grant, and K. F. Dobinson. 2005. Mutations in VMK1, a mitogen-activated protein kinase gene, affect microsclerotia formation and pathogenicity in Verticillium dahliae. Curr. Genet. 48:109-116.[CrossRef][Medline]
    124. 124
  124. Reyes, G., A. Romans, C. K. Nguyen, and G. S. May. 2006. Novel mitogen-activated protein kinase MpkC of Aspergillus fumigatus is required for utilization of polyalcohol sugars. Eukaryot. Cell 5:1934-1940.[Abstract/Free Full Text]
    125. 125
  125. Roman, E., C. Nombela, and J. Pla. 2005. The Sho1 adaptor protein links oxidative stress to morphogenesis and cell wall biosynthesis in the fungal pathogen Candida albicans. Mol. Cell. Biol. 25:10611-10627.[Abstract/Free Full Text]
    126. 126
  126. Rottmann, M., S. Dieter, H. Brunner, and S. Rupp. 2003. A screen in Saccharomyces cerevisiae identified CaMCM1, an essential gene in Candida albicans crucial for morphogenesis. Mol. Microbiol. 47:943-959.[CrossRef][Medline]
    127. 127
  127. Rui, O., and M. Hahn. 2007. The Slt2-type MAP kinase Bmp3 of Botrytis cinerea is required for normal saprotrophic growth, conidiation, plant surface sensing and host tissue colonization. Mol. Plant Pathol. 8:173-184.[CrossRef]
    128. 128
  128. Ruiz-Roldan, M. C., F. J. Maier, and W. Schaefer. 2001. PTK1, a mitogen-activated-protein kinase gene, is required for conidiation, appressorium formation, and pathogenicity of Pyrenophora teres on barley. Mol. Plant-Microbe Interact. 14:116-125.[Medline]
    129. 129
  129. Saito, H., and K. Tatebayashi. 2004. Regulation of the osmoregulatory HOG MAPK cascade in yeast. J. Biochem. 136:267-272.[Abstract/Free Full Text]
    130. 130
  130. Sato, T., T. Watanabe, T. Mikami, and T. Matsumoto. 2004. Farnesol, a morphogenetic autoregulatory substance in the dimorphic fungus Candida albicans, inhibits hyphae growth through suppression of a mitogen-activated protein kinase cascade. Biol. Pharm. Bull. 27:751-752.[CrossRef][Medline]
    131. 131
  131. Scheffer, J., C. B. Chen, P. Heidrich, M. B. Dickman, and P. Tudzynski. 2005. A CDC42 homologue in Claviceps purpurea is involved in vegetative differentiation and is essential for pathogenicity. Eukaryot. Cell 4:1228-1238.[Abstract/Free Full Text]
    132. 132
  132. Schwartz, M. A., and H. D. Madhani. 2004. Principles of map kinase signaling specificity in Saccharomyces cerevisiae. Annu. Rev. Genet. 38:725-748.[CrossRef][Medline]
    133. 133
  133. Segmuller, N., U. Ellendorf, B. Tudzynski, and P. Tudzynski. 2007. BcSak1, a stress-activated mitogen-activated protein kinase, is involved in vegetative differentiation and pathogenicity in Botrytis cinerea. Eukaryot. Cell 6:211-221.[Abstract/Free Full Text]
    134. 134
  134. Smith, D. G., M. D. Garcia-Pedrajas, W. Hong, Z. Y. Yu, S. E. Gold, and M. H. Perlin. 2004. An Ste20 homologue in Ustilago maydis plays a role in mating and pathogenicity. Eukaryot. Cell 3:180-189.[Abstract/Free Full Text]
    135. 135
  135. Solomon, P. S., O. D. C. Waters, J. Simmonds, R. M. Cooper, and R. P. Oliver. 2005. The Mak2 MAP kinase signal transduction pathway is required for pathogenicity in Stagonospora nodorum. Curr. Genet. 48:60-68.[CrossRef][Medline]
    136. 136
  136. Sussman, A., K. Huss, L. C. Chio, S. Heidler, M. Shaw, D. Ma, G. X. Zhu, R. M. Campbell, T. S. Park, P. Kulanthaivel, J. E. Scott, J. W. Carpenter, M. A. Strege, M. D. Belvo, J. R. Swartling, A. Fischl, W. K. Yeh, C. Shih, and X. S. Ye. 2004. Discovery of cercosporamide, a known antifungal natural product, as a selective Pkc1 kinase inhibitor through high-throughput screening. Eukaryot. Cell 3:932-943.[Abstract/Free Full Text]
    137. 137
  137. Thomas, C. F., P. K. Vohra, J. G. Park, V. Puri, A. H. Limper, and T. J. Kottom. 2003. Pneumocystis carinii BCK1 functions in a mitogen-activated protein kinase cascade regulating fungal cell-wall assembly. FEBS Lett. 548:59-68.[CrossRef][Medline]
    138. 138
  138. Thorsen, M., Y. J. Di, C. Tangemo, M. Morillas, D. Ahmadpour, C. Van der Does, A. Wagner, E. Johansson, J. Boman, F. Posas, R. Wysocki, and M. J. Tamas. 2006. The MAPK Hog1p modulates Fps1p-dependent arsenite uptake and tolerance in yeast. Mol. Biol. Cell 17:4400-4410.[Abstract/Free Full Text]
    139. 139
  139. Tsuji, G., S. Fujii, S. Tsuge, T. Shiraishi, and Y. Kubo. 2003. The Colletotrichum lagenarium Ste12-like gene CST1 is essential for appressorium penetration. Mol. Plant-Microbe Interact. 16:315-325.[Medline]
    140. 140
  140. Urban, M., E. Mott, T. Farley, and K. Hammond Kosack. 2003. The Fusarium graminearum MAP1 gene is essential for pathogenicity and development of perithecia. Mol. Plant Pathol. 4:347-359.[CrossRef]
    141. 141
  141. Vallim, M. A., K. Y. Miller, and B. L. Miller. 2000. Aspergillus SteA (sterile12-like) is a homeodomain-C2/H2-Zn+2 finger transcription factor required for sexual reproduction. Mol. Microbiol. 36:290-301.[CrossRef][Medline]
    142. 142
  142. Viaud, M., S. Fillinger, W. Liu, J. S. Polepalli, P. Le Pecheur, A. R. Kunduru, P. Leroux, and L. Legendre. 2006. A class III histidine kinase acts as a novel virulence factor in Botrytis cinerea. Mol. Plant-Microbe Interact. 19:1042-1050.[CrossRef][Medline]
    143. 143
  143. Vohra, P. K., J. G. Park, B. Sanyal, and C. F. Thomas. 2004. Expression analysis of PCSTE3, a putative pheromone receptor from the lung pathogenic fungus Pneumocystis carinii. Biochem. Biophys. Res. Commun. 319:193-199.[CrossRef][Medline]
    144. 144
  144. Voigt, C. A., W. Schafer, and S. Salomon. 2005. A secreted lipase of Fusarium graminearum is a virulence factor required for infection of cereals. Plant J. 42:364-375.[CrossRef][Medline]
    145. 145
  145. Wang, P., C. B. Nichols, K. B. Lengeler, M. E. Cardenas, G. M. Cox, J. R. Perfect, and J. Heitman. 2002. Mating-type-specific and nonspecific PAK kinases play shared and divergent roles in Cryptococcus neoformans. Eukaryot. Cell 1:257-272.[Abstract/Free Full Text]
    146. 146
  146. Wang, P., J. R. Perfect, J. Heitman, and P. Wang. 2000. The G-protein beta subunit GPB1 is required for mating and haploid fruiting in Cryptococcus neoformans. Mol. Cell. Biol. 20:352-362.[Abstract/Free Full Text]
    147. 147
  147. Waugh, M. S., C. B. Nichols, C. M. DeCesare, G. M. Cox, J. Heitman, and J. A. Alspaugh. 2002. Ras1 and Ras2 contribute shared and unique roles in physiology and virulence of Cryptococcus neoformans. Microbiology 148:191-201.[Abstract/Free Full Text]
    148. 148
  148. Wei, H., N. Requena, and R. Fischer. 2003. The MAPKK kinase SteC regulates conidiophore morphology and is essential for heterokaryon formation and sexual development in the homothallic fungus Aspergillus nidulans. Mol. Microbiol. 47:1577-1588.[CrossRef][Medline]
    149. 149
  149. Wiederhold, N. P., D. P. Kontoyiannis, R. A. Prince, and R. E. Lewis. 2005. Attenuation of the activity of caspofungin at high concentrations against Candida albicans: possible role of cell wall integrity and calcineurin pathways. Antimicrob. Agents Chemother. 49:5146-5148.[Abstract/Free Full Text]
    150. 150
  150. Wormley, F. L., G. Heinrich, J. L. Miller, J. R. Perfect, and G. M. Cox. 2005. Identification and characterization of an SKN7 homologue in Cryptococcus neoformans. Infect. Immun. 73:5022-5030.[Abstract/Free Full Text]
    151. 151
  151. Xu, J. R. 2000. MAP kinases in fungal pathogens. Fungal Genet. Biol. 31:137-152.[CrossRef][Medline]
    152. 152
  152. Xu, J. R., C. J. Staiger, and J. E. Hamer. 1998. Inactivation of the mitogen-activated protein kinase MPS1 from the rice blast fungus prevents penetration of host cells but allows activation of plant defense responses. Proc. Natl. Acad. Sci. USA 95:12713-12718.[Abstract/Free Full Text]
    153. 153
  153. Xue, C., G. Park, W. Choi, L. Zheng, R. A. Dean, and J. R. Xu. 2002. Two novel fungal virulence genes specifically expressed in appressoria of the rice blast fungus. Plant Cell 14:2107-2119.[Abstract/Free Full Text]
    154. 154
  154. Xue, C. Y., Y. S. Bahn, G. M. Cox, and J. Heitman. 2006. G protein-coupled receptor Gpr4 senses amino acids and activates the cAMP-PKA pathway in Cryptococcus neoformans. Mol. Biol. Cell 17:667-679.[Abstract/Free Full Text]
    155. 155
  155. Xue, T., C. K. Nguyen, A. Romans, and G. S. May. 2004. A mitogen-activated protein kinase that senses nitrogen regulates conidial germination and growth in Aspergillus fumigatus. Eukaryot. Cell 3:557-560.[Abstract/Free Full Text]
    156. 156
  156. Yue, C. L., L. M. Cavallo, J. A. Alspaugh, P. Wang, G. M. Cox, J. R. Perfect, and J. Heitman. 1999. The STE12 alpha homolog is required for haploid filamentation but largely dispensable for mating and virulence in Cryptococcus neoformans. Genetics 153:1601-1615.[Abstract/Free Full Text]
    157. 157
  157. Zhang, Y., R. Lamm, C. Pillonel, S. Lam, and J. R. Xu. 2002. Osmoregulation and fungicide resistance: the Neurospora crassa OS-2 gene encodes a HOG1 mitogen-activated protein kinase homologue. Appl. Environ. Microbiol. 68:532-538.[Abstract/Free Full Text]
    158. 158
  158. Zhao, X., Y. Kim, G. Park, and J.-R. Xu. 2005. A mitogen-activated protein kinase cascade regulating infection-related morphogenesis in Magnaporthe grisea. Plant Cell 17:1317-1329.[Abstract/Free Full Text]
    159. 159
  159. Zhao, X. H., and J. R. Xu. 2007. A highly conserved MAPK-docking site in Mst7 is essential for Pmk1 activation in Magnaporthe grisea. Mol. Microbiol. 63:881-894.[Medline]
    160. 160
  160. Zheng, L., M. Campbell, J. Murphy, S. Lam, and J. R. Xu. 2000. The BMP1 gene is essential for pathogenicity in the gray mold fungus Botrytis cinerea. Mol. Plant-Microbe Interact. 13:724-732.[Medline]

Eukaryotic Cell, October 2007, p. 1701-1714, Vol. 6, No. 10
1535-9778/07/$08.00+0     doi:10.1128/EC.00216-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Birkaya, B., Maddi, A., Joshi, J., Free, S. J., Cullen, P. J. (2009). Role of the Cell Wall Integrity and Filamentous Growth Mitogen-Activated Protein Kinase Pathways in Cell Wall Remodeling during Filamentous Growth. Eukaryot Cell 8: 1118-1133 [Abstract] [Full Text]  
  • Mosquera, G., Giraldo, M. C., Khang, C. H., Coughlan, S., Valent, B. (2009). Interaction Transcriptome Analysis Identifies Magnaporthe oryzae BAS1-4 as Biotrophy-Associated Secreted Proteins in Rice Blast Disease. Plant Cell 21: 1273-1290 [Abstract] [Full Text]  
  • Park, G., Pan, S., Borkovich, K. A. (2008). Mitogen-Activated Protein Kinase Cascade Required for Regulation of Development and Secondary Metabolism in Neurospora crassa. Eukaryot Cell 7: 2113-2122 [Abstract] [Full Text]  
  • Mehrabi, R., Ding, S., Xu, J.-R. (2008). MADS-Box Transcription Factor Mig1 Is Required for Infectious Growth in Magnaporthe grisea. Eukaryot Cell 7: 791-799 [Abstract] [Full Text]  

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zhao, X.
Right arrow Articles by Xu, J.-R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zhao, X.
Right arrow Articles by Xu, J.-R.

Copyright © 2009 by the American Society for Microbiology.   For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»