Large Scale Identification of Genes Involved in Cell Surface Biosynthesis and Architecture in <i>Saccharomyces cerevisiae</i>

Marc Lussier(McGill University), Ann-Marie White(Center for Cancer Research), Jane Sheraton(McGill University), Tiziano di Paolo(McGill University), Julie Treadwell(McGill University), Susan B. Southard(Center for Cancer Research), C.I. Horenstein(Center for Cancer Research), Joan Chen-Weiner(Center for Cancer Research), Arthur F. J. Ram, Johan C. Kapteyn, Terry Roemer(Yale University), DAHN H. VO(McGill University), Dana C Bondoc(McGill University), John D. Hall(McGill University), Wu Wei Zhong(McGill University), Anne‐Marie Sdicu(McGill University), Julian Davies(University of British Columbia), Frans M. Klis, Phillips W. Robbins(Center for Cancer Research), Howard Bussey(McGill University)
Genetics
October 1, 1997
Cited by 368Open Access
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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.


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