Large Scale Identification of Genes Involved in Cell Surface Biosynthesis and Architecture in Saccharomyces cerevisiae

Author:

Lussier Marc1,White Ann-Marie2,Sheraton Jane1,di Paolo Tiziano1,Treadwell Julie1,Southard Susan B2,Horenstein Craig I2,Chen-Weiner Joan2,Ram Arthur F J3,Kapteyn Johan C3,Roemer Terry W4,Vo Dahn H1,Bondoc Dana C1,Hall John1,Zhong Wu Wei1,Sdicu Anne-Marie1,Davies Julian5,Klis Frans M3,Robbins Phillips W2,Bussey Howard1

Affiliation:

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

2. Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139

3. Institute for Molecular Cell Biology, BioCentrum Amsterdam, 1098 SM Amsterdam, The Netherlands

4. Department of Biology, Yale University, New Haven, Connecticut 06520

5. Department of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia, Canada

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.

Publisher

Oxford University Press (OUP)

Subject

Genetics

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