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Eukaryotic Cell, August 2009, p. 1278-1286, Vol. 8, No. 8
1535-9778/09/$08.00+0     doi:10.1128/EC.00148-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

β-Glucanase Eng2 Is Required for Ascus Wall Endolysis after Sporulation in the Fission Yeast Schizosaccharomyces pombe{triangledown}

Javier Encinar del Dedo, Encarnación Dueñas, Yolanda Arnáiz, Francisco del Rey, and Carlos R. Vázquez de Aldana*

Instituto de Microbiología Bioquímica, Dpto. Microbiología y Genética, CSIC/Universidad de Salamanca, Campus Miguel de Unamuno, 37007 Salamanca, Spain

Received 22 May 2009/ Accepted 16 June 2009

Meiosis is the developmental program by which sexually reproducing diploid organisms generate haploid gametes. In yeast, meiosis is followed by spore morphogenesis. When Schizosaccharomyces pombe diploid cells undergo meiosis, they differentiate into asci containing four haploid ascospores that are highly resistant to environmental stress. The formation of the ascospore wall requires the activity of several enzymes involved in the biosynthesis and modification of its components, such as {alpha}- and β-glucan synthases. Once the spores are completely mature, the wall of the ascus undergoes an endolytic process that results in the release of ascospores from the ascus, allowing their dispersal into the environment. This process requires the activity of the endo-{alpha}-1,3-glucanase Agn2. Here, we focus on the characterization of the endo-β-1,3-glucanase Eng2, which is also required for ascospore release from the ascus. Although Eng2 is present during the mitotic cycle, the protein accumulates after meiosis II. The expression of eng2+ is required for the efficient release of ascospores, as shown by placing eng2+ under the control of a repressible promoter. Furthermore, a point mutation that destroys the catalytic activity of the protein results in a phenotype similar to that of the mutant strain. Finally, we demonstrate that exogenous addition of purified Eng2 releases the ascospores from asci generated by an eng2{Delta} mutant. We propose that Eng2 would act together with Agn2 to completely hydrolyze the ascus wall, thereby assisting in the release of ascospores in S. pombe.

* Corresponding author. Mailing address: Instituto de Microbiología Bioquímica, CSIC/Universidad de Salamanca, Edificio Departamental, Campus Miguel de Unamuno, 37007 Salamanca, Spain. Phone: 34-923-252092. Fax: 34-923-224876. E-mail: cvazquez{at}usal.es

{triangledown} Published ahead of print on 19 June 2009.

Eukaryotic Cell, August 2009, p. 1278-1286, Vol. 8, No. 8
1535-9778/09/$08.00+0     doi:10.1128/EC.00148-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.





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