Large Scale Identification of Genes Involved in Cell Surface Biosynthesis and Architecture in Saccharomyces cerevisiae
Author(s) -
Marc Lussier,
Ann-Marie White,
Jane Sheraton,
Tiziano di Paolo,
Julie Treadwell,
Susan B. Southard,
C.I. Horenstein,
Joan Chen-Weiner,
Arthur F. J. Ram,
Johan C. Kapteyn,
Terry Roemer,
DAHN H. VO,
Dana C Bondoc,
John D. Hall,
Wu Wei Zhong,
AnneMarie Sdicu,
Julian Davies,
Frans M. Klis,
Phillips W. Robbins,
Howard Bussey
Publication year - 1997
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1093/genetics/147.2.435
Subject(s) - biology , gene , saccharomyces cerevisiae , genetics , genome , phenotype , mutant , transposable element , genetic screen , homology (biology)
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.
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