EC Accepts, published online ahead of print on 19 June 2009

This Article Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Google Scholar Articles by Encinar del Dedo, J. Articles by Vázquez de Aldana, C. R. PubMed PubMed Citation Articles by Encinar del Dedo, J. Articles by Vázquez de Aldana, C. R. Pubmed/NCBI databases Substance via MeSH

 Previous Article  |  Next Article 

Eukaryotic Cell doi:10.1128/EC.00148-09
Copyright (c) 2009, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

The -glucanase Eng2 is required for ascus-wall endolysis after sporulation in fission yeast

Javier Encinar del Dedo, M. Encarnación Dueñas-Santero, 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

^* To whom correspondence should be addressed. Email: cvazquez{at}usal.es.

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 - and -glucan synthases. Once the spores are completely mature, the wall of the asci 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--1,3-glucanase Agn2. Here we focus on the characterization of the endo--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 an repressible promoter. Furthermore, a point mutation that destroys the catalytic activity of the protein results in a phenotype similar to the mutant strain. Finally, we demonstrate that exogenous addition of purified Eng2 releases the ascospores from asci generated by an eng2 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.