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Eukaryotic Cell, December 2006, p. 2120-2127, Vol. 5, No. 12
1535-9778/06/$08.00+0     doi:10.1128/EC.00121-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Identification of Translational Regulation Target Genes during Filamentous Growth in Saccharomyces cerevisiae: Regulatory Role of Caf20 and Dhh1

Young-Un Park, Hyangsuk Hur, Minhan Ka, and Jinmi Kim^*

Department of Microbiology, School of Bioscience and Biotechnology, Chungnam National University, Daejeon 305-764, Republic of Korea

Received 21 April 2006/ Accepted 2 October 2006

Top Abstract Introduction Materials and Methods Results Discussion References

 
The dimorphic transition of yeast to the hyphal form is regulated by the mitogen-activated protein kinase and cyclic AMP-dependent protein kinase A pathways in Saccharomyces cerevisiae. Signaling pathway-responsive transcription factors such as Ste12, Tec1, and Flo8 are known to mediate filamentation-specific transcription. We were interested in investigating the translational regulation of specific mRNAs during the yeast-to-hyphal-form transition. Using polyribosome fractionation and RT-PCR analysis, we identified STE12, GPA2, and CLN1 as translation regulation target genes during filamentous growth. The transcript levels for these genes did not change, but their mRNAs were preferentially associated with polyribosomes during the hyphal transition. The intracellular levels of Ste12, Gpa2, and Cln1 proteins increased under hyphal-growth conditions. The increase in Ste12 protein level was partially blocked by mutations in the CAF20 and DHH1 genes, which encode an eIF4E inhibitor and a decapping activator, respectively. In addition, the caf20 and dhh1 mutations resulted in defects in filamentous growth. The filamentation defects caused by caf20 and dhh1 mutations were suppressed by STE12 overexpression. These results suggest that Caf20 and Dhh1 control yeast filamentation by regulating STE12 translation.

Top Abstract Introduction Materials and Methods Results Discussion References

 
The cellular morphology of diploid Saccharomyces cerevisiae frequently switches between the yeast and filamentous forms depending on nutritional signals (16). Several signal transduction modules, including the mitogen-activated protein kinase (MAPK) cascade and the cyclic AMP-dependent protein kinase A (PKA) pathway, are known to participate in this switch (14, 21, 31, 36). The MAPK cascade involves Ste20, Ste11, Ste7, Kss1, and the transcription factors Ste12 and Tec1 (15, 21, 29, 30). The PKA pathway involves Gpr1, Gpa2, Ras2, Tpk2, and the transcription factors Flo8 and Sfl1 (22, 26, 31, 32). These signaling pathways control the transcription of a number of filamentation-specific genes, including FLO11 (19, 23, 29).

Although the signaling pathways and transcriptional regulation of yeast filamentous growth have been studied in considerable detail, little is known about translational regulation related to the transition from the yeast to the filamentous form. In this study, we searched for specific mRNAs that are preferentially translated during the yeast-to-hyphal-form transition. Genome-wide analysis of mRNA translation profiles indicates that the loading of ribosomes onto individual mRNA species varies broadly (20, 28). The association of mRNA transcripts in polyribosomes reflects the rate of synthesis of their corresponding proteins (3, 45). By purifying polyribosome fractions and employing RT-PCR analysis, we found that the mRNA transcripts of STE12, GPA2, and CLN1 were preferentially recruited to polyribosomes during filamentation compared to during normal vegetative growth, even though their levels in the total cell extracts were not changed. Consistently, the protein levels of Ste12, Gpa2, and Cln1 also increased during filamentation. The up-regulation of STE12 mRNA translation during filamentous growth appeared to be partly dependent on CAF20 and DHH1, which encode an eIF4E (the cap-binding protein) inhibitor and an mRNA decapping activator, respectively. Both CAF20 and DHH1 were shown to be important for filamentous growth in yeast.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Strains, plasmids, and growth conditions. The S. cerevisiae strains and plasmids used in this study are listed in Table 1. Standard yeast media were prepared using the established procedure (1). Synthetic low-ammonium medium (SLAD) was prepared as described previously (16). 5-FOA (5-fluoro-orotic acid) medium was composed of 0.67% yeast nitrogen without amino acid, 2% dextrose, and 0.1% 5-FOA (1). Standard methods of yeast transformation and genetic crosses were used for the constructions of all strains.

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TABLE 1. Strains and plasmids used in this study

Cell lysis and polyribosome fractionation. Yeast cells were grown at 30°C in YEPD (yeast extract-peptone-dextrose) or SLAD to an A₆₀₀ of 0.8 to 1.0. Prior to cell collection, cycloheximide was added to a final concentration of 50 µg/ml. Cells were pelleted by centrifugation and washed with 1/30 culture volume of breaking buffer A (BBA; 20 mM Tris-Cl [pH 7.5], 50 mM NaCl, 10 mM MgCl₂, 1 mM dithiothreitol, 50 µg/ml cycloheximide, and 20 µg/ml heparin) on ice (34). Cells were resuspended in 1.5 cell volumes of BBA and lysed by vortexing in the presence of 1 volume of glass beads. Lysates were clarified by centrifugation at 4,200 rpm for 5 min, and the supernatants were centrifuged at 13,000 rpm for 20 min. Twenty-five A₂₆₀ units of lysates were fractionated on 5-to-45% sucrose gradients as described previously (12). Gradients were centrifuged at 35,000 rpm in an SW41 rotor (Beckman) at 4°C for 3.5 h and were then fractionated with monitoring of A₂₅₄.

RNA analysis and RT-PCR. Total RNA was isolated from each fraction with an RNeasy kit (QIAGEN). cDNA synthesis was performed using 20 µg/ml RNA in 10 µg/ml oligo(dT), 50 mM Tris-Cl (pH 8.3), 75 mM KCl, 3 mM MgCl₂, 10 mM dithiothreitol, 2.5 mM deoxynucleoside triphosphates (dNTPs), and Moloney murine leukemia virus reverse transcriptase (Gibco BRL). Reactions were carried out at 37°C for 1 h and followed by heat inactivation at 75°C for 30 min. Each PCR was performed using 5 µl of the cDNA reaction mixture, 2.5 mM dNTPs, 1 unit of Taq polymerase, and a pair of gene-specific PCR primers (40 pmol). The amplification was carried out through 30 cycles at 94°C for 30 s, at 52°C for 30 s, and at 72°C for 50 s.

Tagging genes with HA. For tagging target genes with three hemagglutinins, we used an HA-URA3-HA cassette of the pQF296.10 plasmid as described previously (17). The HA integration sites of Flo8-HA and Flo11-HA proteins were as described previously (17, 22). The HA tagging of Gpa2-HA, Ste12-HA, and Cln1-HA proteins was C terminal (see Fig. 2A). The HA-URA3-HA region was PCR amplified using the DNA of the pQF296.10 plasmid as a template and a pair of primers for each target gene. The PCR products were transformed into the 10560-2B strain. Integration of a HA-URA3-HA cassette at each target open reading frame was confirmed by PCR analysis. The URA3 pop-outs from homologous recombination were selected on a 5-FOA plate.

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FIG. 2. Construction of HA-tagged strains. (A) Structures of Flo11-HA, Gpa2-HA, Ste12-HA, Cln1-HA, and Flo8-HA proteins. The HA integration site of each construction is indicated. (B) Functional assays of HA-tagged genes. Haploid invasive phenotypes were tested with patches of yeast strains (wild-type strain 10560-2B and HA-tagged strains JK371 to JK375) on solid-agar plates. After incubation, the plates were photographed before (top) and after (bottom) the cells were washed.

Immunoblot analysis. Total protein preparation and immunoblotting were conducted as previously described (18). HA-tagged proteins were detected with the anti-HA monoclonal antibody 12CA5 (1:1,000 dilution; Boehringer Mannheim). The tubulin proteins were detected using an Anti-Tubulin Cocktail (InnoGenex). HRP-conjugated anti-mouse antibody was utilized as a secondary antibody.

Northern blot analysis. Total RNA was prepared as previously described (10). Twenty micrograms of total yeast RNA was fractionated by electrophoresis through a 1.0% formaldehyde gel and was subsequently transferred to a Nytran membrane (Hoefer). Blotting was performed as described elsewhere (38). The PCR products of FLO11 (ORF 3541 to 4074), GPA2 (408 to 1164), STE12 (1095 to 1759), CLN1 (428 to 1165), FLO8 (1081 to 1979), and ACT1 (49 to 770) were used as probes. Probes were labeled with a Random Prime labeling system (Amersham).

Construction of deletion mutants. Deletion mutations of CAF20, DHH1, and TIF1 were constructed using PCR-based gene disruption methods (27, 44). The disruption marker LEU2 was PCR amplified using primers containing a 51-bp sequence homologous to the target gene and an 18-bp sequence from the LEU2 marker. The PCR products were transformed into a haploid strain of the a or mating type. Integration of LEU2 at each gene was confirmed by PCR analysis of genomic DNA from each transformant.

Top Abstract Introduction Materials and Methods Results Discussion References

 
STE12, GPA2, and CLN1 mRNA transcripts are preferentially recruited to polyribosomes under filamentous-growth conditions. Little is known about the translational regulation of specific mRNAs during the yeast-to-hyphal-form transition. Based on the finding that actively translated mRNAs are associated with polyribosomes, we analyzed the polyribosomal mRNAs and searched for genes actively translated during hyphal induction. A diploid yeast strain was cultured in either YEPD medium (yeast form) or SLAD (pseudohyphal form) at 30°C for 8 h. At this time point, cells in SLAD are in the early stage of the hyphal transition. This is sufficient to induce hyphal-form-specific gene expression. Total cellular mRNAs were fractionated through a 5-to-45% sucrose gradient, and the abundance of target mRNAs in polyribosomal fractions was analyzed by RT-PCR using gene-specific primers (Fig. 1). The specific mRNA molecules examined include those of two protein kinases (Ste20 and Ste11), five transcription factors (Ste12, Tec1, Flo8, Msn1, and Mss11), a cyclin (Cln1), two membrane-bound signaling molecules (Mep2 and Gpa2), and the cell surface protein Flo11 (13, 14, 24, 26). As shown previously (23), the levels of FLO11 total RNAs were higher under conditions promoting hyphal growth than conditions promoting yeast growth (Fig. 1A). Accordingly, polyribosomal FLO11 mRNAs were more abundant in the hyphal culture than the yeast culture (Fig. 1C). Importantly, we found that even though the mRNA levels of STE12, GPA2, and CLN1 were not induced under nitrogen starvation conditions (Fig. 1A), these transcripts were enriched in the polyribosomal fractions (Fig. 1C). Total and polysomal levels of FLO8 mRNA did not change during the yeast-to-hyphal-form transition. Similarly, the transcripts of six other genes (STE20, STE11, TEC1, MSN1, MSS11, and MEP2) were not enriched in the polyribosomal fractions (data not shown). These results suggest that the mRNA of STE12, GPA2, and CLN1 were preferentially recruited to polyribosomes for translation during the yeast pseudohyphal differentiation.

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FIG. 1. Polyribosomal profiles of FLO11, GPA2, STE12, CLN1, and FLO8 mRNAs in yeast and pseudohyphal cultures. (A) Total RNAs of FLO11, GPA2, STE12, CLN1, and FLO8 from YEPD (yeast form) and SLAD (pseudohyphal-form) cultures analyzed by RT-PCR. (B) Polyribosome fractionations. Cell lysates from YEPD or SLAD cultures were analyzed by sucrose gradient sedimentation at 35,000 rpm at 4°C for 3.5 h. (C) RT-PCR analysis of FLO11, GPA2, STE12, CLN1, and FLO8 mRNAs from polyribosomal fractions. Lanes 1 to 8 correspond to the fraction numbers in panel B. RT-PCR was performed with a set of gene-specific primers.

Ste12, Gpa2, and Cln1 protein levels increase during filamentous growth. To determine whether the levels of Ste12, Gpa2, and Cln1 proteins increase during the yeast-to-hyphal-form transition, we inserted the HA epitope into the chromosome copy of the FLO11, STE12, GPA2, CLN1, and FLO8 genes in a haploid strain (see Materials and Methods). All of the HA-tagged genes except GPA2 appeared to be functional in the filamentous phenotype, as assayed by a haploid invasive-growth test (Fig. 2). Diploid strains, which were constructed by mating the HA-tagged strains with the opposite mating type, behaved like a wild-type strain in a pseudohyphal-growth test (data not shown).

HA-tagged diploid strains were grown to the late exponential phase. The cultures were then shifted to filamentation-inducing medium (SLAD), and total protein was isolated after 2, 4, and 8 h. At the 4- and 8-h time points, the level of Flo11-HA protein in the hyphal culture was higher than in the yeast form (Fig. 3A). Northern blotting showed that the level of FLO11 transcripts was also increased in the hyphal culture (Fig. 3B). These results confirm the previous finding that FLO11 induction is at the transcriptional level. The levels of Ste12-HAp, Gpa2-HAp, and Cln1-HAp increased during pseudohyphal growth, but their transcript levels remained unchanged (Fig. 3B). These results correlated with an enrichment of STE12, GPA2, and CLN1 mRNAs in the polyribosome fractions. The level of Flo8-HAp was the same under yeast and pseudohyphal-form growth conditions. These results suggest that expression of STE12, GPA2, and CLN1 is controlled at the translational level during the yeast-to-pseudohyphal-form transition.

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FIG. 3. Increased levels of Gpa2, Ste12, and Cln1 proteins during the pseudohyphal transition. (A) Western blots of Flo11-HA (JK376), Gpa2-HA (JK377), Ste12-HA (JK378), Cln1-HA (JK379), and Flo8-HA (JK380) strains in YEPD medium or SLAD. Tubulins, commonly used as a loading control, showed an increase in the protein level in SLAD. Flo8-HA showed a constant level of proteins. (B) Northern blots of Flo11-HA, Gpa2-HA, Ste12-HA, Cln1-HA, and Flo8-HA strains in YEPD medium or SLAD. Act1 is a loading control.

Caf20 and Dhh1 regulate STE12 expression during filamentous growth. We next considered whether any components of the translational machinery play a regulatory role in expression of STE12. Deletion mutations of CAF20 (eIF4E-binding protein) or TIF1 (eIF4A) were constructed in strain 1278b, commonly used for studying filamentous growth. At the early step of translation initiation, the cap-binding protein eIF4E binds to m⁷G caps at the 5' termini of mRNA and subsequently associates with eIF4G (33, 43). Caf20 is known to compete with eIF4G for binding to eIF4E and to inhibit cap-dependent translation (2, 9, 35). The RNA helicase eIF4A is another binding partner of eIF4G and is thought to unwind the 5' secondary structure of mRNA. Two duplicate genes, TIF1 and TIF2, encode eIF4A, and disruption of both is lethal to the cell (39). As shown in Fig. 4A, caf20/caf20 and tif1/tif1 diploid mutant strains showed lower levels of Ste12-HAp than the wild type under filamentous-growth conditions. The relative levels of Ste12p were 0.53 for caf20 and 0.74 for tif1 (Fig. 4B). The effects of the caf20 or tif1 mutations did not appear to be due to general translational repression in the filamentation-inducing medium, because these mutations did not affect the level of Cln1-HAp or Flo8-HAp.

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FIG. 4. Effects of caf20, dhh1, and tif1 mutations on the induction of Ste12-HA protein during the pseudohyphal transition. (A) Western blots of Ste12-HA, Cln1-HA, and Flo8-HA. Plasmid pJI255 (STE12-HA), pJI256 (CLN1-HA), or pJI257 (FLO8-HA) was introduced into wild-type strain JK353 and mutant diploid strains JK383 (caf20/caf20), JK386 (tif1/tif1), JK354 (kem1/kem1), and JK389 (dhh1/dhh1). After growth for 8 h in YEPD medium or SLAD, total proteins were analyzed by Western blotting. (B) Relative levels of Ste12-HA protein in SLAD. The results are averages for three independent Western experiments. (C) Northern blots of STE12-HA in SLAD.

The regulation of translation initiation and the stability of mRNAs are intimately linked (41). We asked whether mutations in mRNA decapping or degradation enzymes affect the expression of STE12. Previously, our group reported that the deletion mutation of KEM1/XRN1, which encodes a major cytoplasmic 5'-3' exoribonuclease, causes a defect in haploid invasive and diploid filamentous growth (18). DHH1 encodes a DEAD box RNA helicase and has been reported to be an activator of decapping (8, 11). DHH1 and KEM1/XRN1 have been shown to be the components of the mRNA processing bodies (5, 25). Recent results suggest that Dhh1 also functions as a repressor of translation (7). The level of Ste12 protein was examined in the dhh1/dhh1 and kem1/kem1 mutant strains. As shown in Fig. 4A, the kem1 mutation did not affect the level of Ste12 protein under filamentous-growth conditions. These results rule out the possibility that the kem1 mutation affects the stability of STE12 mRNAs and thus alters STE12 expression. In the dhh1/dhh1 mutant strains, the Ste12p level did not increase during filamentation. The level of Ste12p in dhh1 mutant cells was 0.14 relative to that in the wild type (Fig. 4B). Northern blotting showed that the caf20, dhh1, and tif1 mutations have no effect on STE12-HA transcripts (Fig. 4C). Our results suggest that CAF20, DHH1, and TIF1 are required for STE12 expression at the protein level during filamentous growth.

caf20/caf20 and dhh1/dhh1 mutants show defects in filamentous growth. The transcription factor Ste12 is essential for activation of filamentation-specific genes. We investigated whether the low levels of Ste12 protein in caf20/caf20, dhh1/dhh1, and tif1/tif1 mutant cells result in defects in filamentous growth. Pseudohyphal phenotypes of these mutant strains were tested. The colony morphologies on SLAD were examined before and after washing (Fig. 5A). The caf20/caf20 mutants exhibited pseudohyphal colony morphology with an unusual colony edge. The differences from the wild type were more evident in the agar invasion phenotype. The dhh1/dhh1 mutants were defective in the pseudohyphal colony morphologies and agar invasion phenotypes. The tif1/tif1 mutants, however, did not show any defects in the pseudohyphal phenotypes.

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FIG. 5. Pseudohyphal defects of caf20/caf20 and dhh1/dhh1 mutant strains. (A) Colony morphologies. Wild-type strain JK353 and mutant strains JK383 (caf20/caf20), JK386 (tif1/tif1), and JK389 (dhh1/dhh1) were tested on SLAD plates. After 5 days of incubation, the colonies were photographed before (top) and after (bottom) cells were washed off the agar plate. (B) Enlarged view of the cells on the SLAD plate after 10 h of incubation.

We next examined the cellular morphologies on the SLAD plates by light microscopy (Fig. 5B). After 10 h, the colony-forming cells of the wild-type strain were elongated and formed pseudohyphae, whereas caf20/caf20 and dhh1/dhh1 cells were in the yeast form. These results indicate that caf20 and dhh1 mutations show defects in pseudohyphal development.

Invasive growth of the haploid mutant strains was tested on YEPD medium (Fig. 6A). The caf20 and dhh1 mutants were markedly defective in invasive growth. The invasive growth of the tif1 mutant, however, was similar to that of the wild type. The invasive-growth phenotypes of the mutant strains were in good correlation with FLO11-lacZ expression in the mutant cells (Fig. 6B). These results indicate that CAF20 and DHH1 play critical roles in both haploid invasive growth and diploid pseudohyphal development.

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FIG. 6. Invasive-growth defect of caf20 and dhh1 mutants. (A) Wild-type strain 10560-2B and mutant strains JK381 (caf20), JK384 (tif1), and JK387 (dhh1) were tested on YEPD. Cell suspensions of each strain were applied to the plates and incubated for 3 days. The plates were photographed before and after cells were washed off the agar surface. (B) The ß-galactosidase activities of plasmid FLO11-lacZ were measured in wild-type strain 10560-2B and mutant strains JK381 (caf20), JK384 (tif1), and JK387 (dhh1). ß-Galactosidase assays were essentially the same as previously described (40).

Filamentous growth defects caused by caf20/caf20 and dhh1/dhh1 mutations are suppressed by overexpression of STE12. To determine whether the overexpression of STE12 suppresses the filamentation defects caused by caf20 and dhh1 mutations, we introduced a 2µ-based plasmid carrying STE12 with its own promoter into diploid mutant strains. As shown in Fig. 7A, STE12 overexpression restored both the filamentous colony morphology and the agar invasion phenotype to the caf20/caf20 and dhh1/dhh1 mutant strains. The level of Ste12p in each overexpressing strain, which was analyzed with the STE12-HA allele, was consistent with its suppression phenotype (Fig. 7B). STE12 overexpression enhanced filamentation in the caf20/caf20 strain to nearly the same extent as in the wild-type strain. STE12 overexpression in the dhh1/dhh1 strain, by contrast, only slightly enhanced filamentation and resulted in a reduced colony size. On the basis of these results, we propose that the filamentation phenotypes in the caf20/caf20 and dhh1/dhh1 mutant strains are closely related to their low levels of Ste12p.

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FIG. 7. Suppression of caf20 and dhh1 mutations by overexpression of STE12. (A) Pseudohyphal phenotypes of caf20/caf20 and dhh1/dhh1 mutant strains carrying the STE12 overexpression plasmid. A wild-type strain (JK353) and mutant strains JK383 (caf20/caf20) and JK389 (dhh1/dhh1) were transformed with vector pRS426 or 2µ STE12 (pJI274) and tested on SLAD plates. After 5 days of incubation, the colony morphology was photographed before (top) and after (bottom) cells were washed off the agar plate. The caf20/caf20 strain with the CAF20 plasmid (pJI276) and the dhh1/dhh1 strain with the DHH1 plasmid (pJI277) were also included. (B) Ste12p levels in caf20/caf20 and dhh1/dhh1 mutant strains carrying the STE12 overexpression plasmid. Wild-type strain JK353 and mutant strains JK383 (caf20/caf20) and JK389 (dhh1/dhh1) carrying either pJI255 (CEN STE12::HA) or pJI274 (2µ STE12::HA) were grown for 8 h in SLAD. Total proteins were analyzed by Western blotting.

Top Abstract Introduction Materials and Methods Results Discussion References

 
The signaling pathways and the transcriptional regulations associated with filamentous growth of S. cerevisiae have been analyzed in considerable detail, but understanding of the regulation at the protein level is limited (14, 19, 21). Here, we identified three genes, STE12, GPA2, and CLN1, that are up-regulated at the protein level during the yeast-to-pseudohyphal-form transition. The increased levels of these proteins could be due to increased translation or greater protein stability. On the basis of our data, it is likely that these regulations are at the translational level. Polyribosomal mRNAs for STE12, GPA2, and CLN1 were abundant under hyphal-culture conditions, indicating that they were actively translated. We also showed that Caf20, which is a cap-dependent translation inhibitor, is involved in the up-regulation of Ste12 protein during filamentous growth.

Our findings suggest for the first time that CAF20 and DHH1 participate in filamentous growth. The 4E-BPs, which were the first eIF4E-inhibitory proteins discovered, modulate eIF4E-eIF4G interaction by sequestering available eIF4E (35). In S. cerevisiae, Caf20 was found to be equivalent to 4E-BPs (2). Deletion of CAF20 increases the growth rate in rich media and partially suppresses the effects of mutations in translation initiation factors (2, 9). In vitro translation assays show that p20 inhibits the translation of capped reporter mRNAs (2). There have been fewer studies on the significance of Caf20 as a cap-dependent translation repressor in S. cerevisiae than in cells of higher eukaryotes. Dhh1 was previously reported as a decapping activator but was recently shown also to function as a translational repressor (7, 8, 11). Our finding that the level of the Ste12 protein does not increase in the caf20/caf20 or dhh1/dhh1 mutant cells implies that Caf20 and Dhh1, previously known as general translational repressors, play positive roles in the up-regulation of Ste12 protein under filamentous-growth conditions.

The low level of Ste12p in caf20/caf20 and dhh1/dhh1 mutant cells appeared to be the main reason for the filamentation defects, because overexpression of STE12 in caf20/caf20 and dhh1/dhh1 mutant cells restored the filamentation phenotypes. Each of these mutants, however, has a different phenotype. The caf20/caf20 mutant strain showed a reduced invasiveness, whereas the dhh1/dhh1 mutant strain had a more severe defect in filamentation. In addition, overexpression of STE12 in the dhh1/dhh1 mutant strain resulted in a synthetic phenotype (i.e., reduced colony size) (Fig. 7A). In the present study, we observed mainly a reduced level of Ste12p in the caf20/caf20 or dhh1/dhh1 mutant strains, but it remains possible that the caf20 or dhh1 mutation could affect expression of other filamentation-associated genes, such as SFL1, TEC1, etc. (29, 32). In addition, DHH1 has been implicated in a number of cellular processes, including mRNA decapping, deadenylation, transcription, and G₁/S cell cycle arrest (4, 8). Further analysis of the role of CAF20 and DHH1 in filamentous growth and STE12 expression, therefore, should help clarifying their roles in yeast cells.

Three genes, STE12, GPA2, and CLN1, were identified in our screening as genes that are up-regulated at the protein level during filamentous growth. We observed that the caf20 and dhh1 mutations did not affect the level of Cln1p. These results imply that the up-regulation of CLN1 mRNA translation is independent of CAF20 and DHH1. The Cln1p level appeared to be further increased by the STE11-4 hyperactive allele under the filamentous-growth conditions, whereas the Ste12p level was not affected by this allele (data not shown). These results suggest that different mechanisms regulate CLN1 and STE12 expression. We are currently investigating other components of the translation initiation and mRNA decay pathways that appear to participate in translational regulation during filamentation.

 
We thank Gerald. R. Fink and Haoping Liu for strains and plasmids and Alan G. Hinnebusch for helpful advice on polyribosome fractionation.

This work was supported by a grant from the Korean Science and Engineering Foundation (R04-2000-000-00040-0) and the Korea Research Foundation Grant, funded by the Korean Government (MOEHRD) (KRF-2004-041-C00350), to J. Kim.

 
* Corresponding author. Mailing address: Department of Microbiology, School of Bioscience and Biotechnology, Chungnam National University, Yuseong-Gu, Gung-Dong 220, Daejeon 305-764, Republic of Korea. Phone: 82-42-821-6416. Fax: 82-42-822-7367. E-mail: jmkim{at}cnu.ac.kr.

Published ahead of print on 13 October 2006.

Top Abstract Introduction Materials and Methods Results Discussion References

 

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Eukaryotic Cell, December 2006, p. 2120-2127, Vol. 5, No. 12
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