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New Approach to Identification of Genes Controlling Cell Wall Biogenesis in the Yeast Saccharomyces cerevisiae

机译:鉴定啤酒酵母中控制细胞壁生物发生的基因的新方法

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摘要

MCD4 codes for a protein presumably adding the phosphoethanolamine moiety to the first mannose residue of glycosylphosphatidylinositol (GPI) precursors in the yeast Saccharomyces cerevisiae.The role of this modification is still unclear.The phenotypic effects of some MCD4 mutations are probably unrelated to defects in GPI synthesis,suggesting additional functions for Mcd4p.To study the Mcd4p functions in more detail,a search for the genes whose mutations are lethal or semilethal in combination with the ssu21 mutation of MCD4 was performed.Six such mutations were isolated,including some mutations causing sensitivity to SDS and/or calcofluor white.Genes complementing two out of the six mutations were cloned and identified as MNN9,which is involved in the formation of outer chains of N-linked glycans of secreted proteins,and GWT1,which codes for an endoplasmic reticulum protein involved in GPI biosynthesis.In both cases,growth inhibition was probably caused by defective biogenesis of the cell wall and a misfolding of secreted proteins.The proposed approach is suitable for seeking new genes controlling cell wall biogenesis.
机译:MCD4编码一种蛋白质,可能是将磷酸乙醇胺部分添加到了酿酒酵母中的糖基磷脂酰肌醇(GPI)前体的第一个甘露糖残基上,这种修饰的作用尚不清楚,某些MCD4突变的表型效应可能与GPI的缺陷无关为了进一步研究Mcd4p的功能,结合MCD4的ssu21突变进行了具有致命或半致命突变的基因的搜索。分离出六个这样的突变,包括一些引起敏感性的突变。克隆到六个突变中的两个互补的基因,并将其鉴定为MNN9和GWT1,其中MNN9与分泌蛋白的N-连接聚糖的外链形成有关,GWT1编码内质网在两种情况下,生长抑制都可能是由GPI生物合成的缺陷引起的。细胞壁和分泌蛋白的错误折叠。该方法适用于寻找控制细胞壁生物发生的新基因。

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