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酿酒酵母中参与细胞表面生物合成和结构的基因的大规模鉴定。

Large scale identification of genes involved in cell surface biosynthesis and architecture in Saccharomyces cerevisiae.

作者信息

Lussier M, White A M, Sheraton J, di Paolo T, Treadwell J, Southard S B, Horenstein C I, Chen-Weiner J, Ram A F, Kapteyn J C, Roemer T W, Vo D H, Bondoc D C, Hall J, Zhong W W, Sdicu A M, Davies J, Klis F M, Robbins P W, Bussey H

机构信息

Department of Biology, McGill University, Montréal, Québec, Canada.

出版信息

Genetics. 1997 Oct;147(2):435-50. doi: 10.1093/genetics/147.2.435.

DOI:10.1093/genetics/147.2.435
PMID:9335584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1208169/
Abstract

The sequenced yeast genome offers a unique resource for the analysis of eukaryotic cell function and enables genome-wide screens for genes involved in cellular processes. We have identified genes involved in cell surface assembly by screening transposon-mutagenized cells for altered sensitivity to calcofluor white, followed by supplementary screens to further characterize mutant phenotypes. The mutated genes were directly retrieved from genomic DNA and then matched uniquely to a gene in the yeast genome database. Eighty-two genes with apparent perturbation of the cell surface were identified, with mutations in 65 of them displaying at least one further cell surface phenotype in addition to their modified sensitivity to calcofluor. Fifty of these genes were previously known, 17 encoded proteins whose function could be anticipated through sequence homology or previously recognized phenotypes and 15 genes had no previously known phenotype.

摘要

测序的酵母基因组为真核细胞功能分析提供了独特的资源,并能够对参与细胞过程的基因进行全基因组筛选。我们通过筛选转座子诱变细胞对荧光增白剂的敏感性变化来鉴定参与细胞表面组装的基因,随后进行补充筛选以进一步表征突变体表型。突变基因直接从基因组DNA中获取,然后与酵母基因组数据库中的基因进行唯一匹配。我们鉴定出了82个明显影响细胞表面的基因,其中65个基因的突变除了对荧光增白剂的敏感性改变外,还表现出至少一种其他细胞表面表型。这些基因中有50个是先前已知的,17个编码的蛋白质其功能可通过序列同源性或先前识别的表型预测,还有15个基因以前没有已知的表型。

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本文引用的文献

1
Completion of the Saccharomyces cerevisiae genome sequence allows identification of KTR5, KTR6 and KTR7 and definition of the nine-membered KRE2/MNT1 mannosyltransferase gene family in this organism.酿酒酵母基因组序列的完成使得KTR5、KTR6和KTR7得以鉴定,并明确了该生物体中由九个成员组成的KRE2/MNT1甘露糖基转移酶基因家族。
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Life with 6000 genes.拥有6000个基因的生命。
Science. 1996 Oct 25;274(5287):546, 563-7. doi: 10.1126/science.274.5287.546.
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Green fluorescent protein as a marker for gene expression and subcellular localization in budding yeast.绿色荧光蛋白作为芽殖酵母中基因表达和亚细胞定位的标记物。
Yeast. 1996 Jun 30;12(8):773-86. doi: 10.1002/(SICI)1097-0061(19960630)12:8%3C773::AID-YEA972%3E3.0.CO;2-L.
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The identification of transposon-tagged mutations in essential genes that affect cell morphology in Saccharomyces cerevisiae.在酿酒酵母中鉴定影响细胞形态的必需基因中的转座子标签突变。
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Stepwise assembly of the lipid-linked oligosaccharide in the endoplasmic reticulum of Saccharomyces cerevisiae: identification of the ALG9 gene encoding a putative mannosyl transferase.酿酒酵母内质网中脂质连接寡糖的逐步组装:编码假定甘露糖基转移酶的ALG9基因的鉴定。
Proc Natl Acad Sci U S A. 1996 Jul 9;93(14):7160-5. doi: 10.1073/pnas.93.14.7160.
9
Genetic analysis of the bipolar pattern of bud site selection in the yeast Saccharomyces cerevisiae.酿酒酵母芽殖位点选择双极模式的遗传分析。
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