Ragni Enrico, Coluccio Alison, Rolli Eleonora, Rodriguez-Peña José Manuel, Colasante Gaia, Arroyo Javier, Neiman Aaron M, Popolo Laura
Dipartimento di Scienze Biomolecolari e Biotecnologie, Università degli Studi di Milano, Via Celoria 26, 20133 Milano, Italy.
Eukaryot Cell. 2007 Feb;6(2):302-16. doi: 10.1128/EC.00321-06. Epub 2006 Dec 22.
The GAS multigene family of Saccharomyces cerevisiae is composed of five paralogs (GAS1 to GAS5). GAS1 is the only one of these genes that has been characterized to date. It encodes a glycosylphosphatidylinositol-anchored protein functioning as a beta(1,3)-glucan elongase and required for proper cell wall assembly during vegetative growth. In this study, we characterize the roles of the GAS2 and GAS4 genes. These genes are expressed exclusively during sporulation. Their mRNA levels showed a peak at 7 h from induction of sporulation and then decreased. Gas2 and Gas4 proteins were detected and reached maximum levels between 8 and 10 h from induction of sporulation, a time roughly coincident with spore wall assembly. The double null gas2 gas4 diploid mutant showed a severe reduction in the efficiency of sporulation, an increased permeability of the spores to exogenous substances, and production of inviable spores, whereas the single gas2 and gas4 null diploids were similar to the parental strain. An analysis of spore ultrastructure indicated that the loss of Gas2 and Gas4 proteins affected the proper attachment of the glucan to the chitosan layer, probably as a consequence of the lack of coherence of the glucan layer. The ectopic expression of GAS2 and GAS4 genes in a gas1 null mutant revealed that these proteins are redundant versions of Gas1p specialized to function in a compartment at a pH value close to neutral.
酿酒酵母的GAS多基因家族由五个旁系同源基因(GAS1至GAS5)组成。GAS1是迄今为止已被表征的这些基因中唯一的一个。它编码一种糖基磷脂酰肌醇锚定蛋白,作为β(1,3)-葡聚糖延伸酶发挥作用,并且在营养生长期间正确的细胞壁组装中是必需的。在本研究中,我们表征了GAS2和GAS4基因的作用。这些基因仅在孢子形成过程中表达。它们的mRNA水平在诱导孢子形成后7小时达到峰值,然后下降。Gas2和Gas4蛋白被检测到,并在诱导孢子形成后8至10小时达到最高水平,这个时间大致与孢子壁组装一致。双缺失gas2 gas4二倍体突变体的孢子形成效率严重降低,孢子对外源物质的通透性增加,并且产生不可存活的孢子,而单缺失gas2和gas4的二倍体与亲本菌株相似。对孢子超微结构的分析表明,Gas2和Gas4蛋白的缺失影响了葡聚糖与壳聚糖层的正确附着,这可能是由于葡聚糖层缺乏连贯性所致。GAS2和GAS4基因在gas1缺失突变体中的异位表达表明,这些蛋白是Gas1p的冗余版本,专门在接近中性pH值的区室中发挥作用。