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1:
Nature.
1999 Nov 25;402(6760):413-8.
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Comment in:
Nature. 1999 Nov 25;402(6760):362-3.
Large-scale analysis of the yeast genome by transposon tagging and gene disruption.
Ross-Macdonald P
,
Coelho PS
,
Roemer T
,
Agarwal S
,
Kumar A
,
Jansen R
,
Cheung KH
,
Sheehan A
,
Symoniatis D
,
Umansky L
,
Heidtman M
,
Nelson FK
,
Iwasaki H
,
Hager K
,
Gerstein M
,
Miller P
,
Roeder GS
,
Snyder M
.
Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520-8103, USA.
Economical methods by which gene function may be analysed on a genomic scale are relatively scarce. To fill this need, we have developed a transposon-tagging strategy for the genome-wide analysis of disruption phenotypes, gene expression and protein localization, and have applied this method to the large-scale analysis of gene function in the budding yeast Saccharomyces cerevisiae. Here we present the largest collection of defined yeast mutants ever generated within a single genetic background--a collection of over 11,000 strains, each carrying a transposon inserted within a region of the genome expressed during vegetative growth and/or sporulation. These insertions affect nearly 2,000 annotated genes, representing about one-third of the 6,200 predicted genes in the yeast genome. We have used this collection to determine disruption phenotypes for nearly 8,000 strains using 20 different growth conditions; the resulting data sets were clustered to identify groups of functionally related genes. We have also identified over 300 previously non-annotated open reading frames and analysed by indirect immunofluorescence over 1,300 transposon-tagged proteins. In total, our study encompasses over 260,000 data points, constituting the largest functional analysis of the yeast genome ever undertaken.
Publication Types:
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
PMID: 10586881 [PubMed - indexed for MEDLINE]
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