Functional profiling of the Saccharomyces cerevisiae genome

被引:3169
作者
Giaever, G
Chu, AM
Ni, L
Connelly, C
Riles, L
Véronneau, S
Dow, S
Lucau-Danila, A
Anderson, K
André, B
Arkin, AP
Astromoff, A
El Bakkoury, M
Bangham, R
Benito, R
Brachat, S
Campanaro, S
Curtiss, M
Davis, K
Deutschbauer, A
Entian, KD
Flaherty, P
Foury, F
Garfinkel, DJ
Gerstein, M
Gotte, D
Güldener, U
Hegemann, JH
Hempel, S
Herman, Z
Jaramillo, DF
Kelly, DE
Kelly, SL
Kötter, P
LaBonte, D
Lamb, DC
Lan, N
Liang, H
Liao, H
Liu, L
Luo, CY
Lussier, M
Mao, R
Menard, P
Ooi, SL
Revuelta, JL
Roberts, CJ
Rose, M
Ross-Macdonald, P
Scherens, B
机构
[1] Stanford Univ, Stanford Genome Technol Ctr, Palo Alto, CA 94304 USA
[2] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA 94305 USA
[3] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[4] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[5] Johns Hopkins Univ, Sch Med, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
[6] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[7] McGill Univ, Dept Biol, Montreal, PQ H3A 1B1, Canada
[8] Rosetta Inpharmat Inc, Kirkland, WA 98034 USA
[9] Catholic Univ Louvain, FYSA, B-1348 Louvain, Belgium
[10] Free Univ Brussels, Lab Physiol Cellulaire, Gosselies, Belgium
[11] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[12] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[13] Univ Calif Berkeley, Lawrence Berkeley Lab, Phys Biosci Div, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[14] Free Univ Brussels, IRMW, B-1070 Brussels, Belgium
[15] Univ Salamanca, CSIC, Inst Microbiol & Bioquim, Dept Genet & Microbiol, E-37007 Salamanca, Spain
[16] Univ Basel, Biozentrum, Dept Mol Microbiol, CH-4056 Basel, Switzerland
[17] Univ Padua, Dept Biol, I-35121 Padua, Italy
[18] Goethe Univ Frankfurt, Inst Microbiol, EUROSCARF, D-60439 Frankfurt, Germany
[19] Univ Calif Berkeley, Dept Elect Engn & Comp Sci, Berkeley, CA 94720 USA
[20] NCI, Ctr Canc Res, Gene Regulat & Chromosome Biol Lab, Frederick, MD 21702 USA
[21] Univ Dusseldorf, Inst Mikrobiol, D-40225 Dusseldorf, Germany
[22] Univ Wales, Inst Biol Sci, Aberystwyth SY23 3DA, Dyfed, Wales
[23] Concordia Univ, Dept Biol, Montreal, PQ H3G 1M8, Canada
[24] Katholieke Univ Leuven, Lab Gene Technol, B-3001 Heverlee, Belgium
基金
英国医学研究理事会;
关键词
D O I
10.1038/nature00935
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Determining the effect of gene deletion is a fundamental approach to understanding gene function. Conventional genetic screens exhibit biases, and genes contributing to a phenotype are often missed. We systematically constructed a nearly complete collection of gene-deletion mutants (96% of annotated open reading frames, or ORFs) of the yeast Saccharomyces cerevisiae. DNA sequences dubbed 'molecular bar codes' uniquely identify each strain, enabling their growth to be analysed in parallel and the fitness contribution of each gene to be quantitatively assessed by hybridization to high-density oligonucleotide arrays. We show that previously known and new genes are necessary for optimal growth under six well-studied conditions: high salt, sorbitol, galactose, pH 8, minimal medium and nystatin treatment. Less than 7% of genes that exhibit a significant increase in messenger RNA expression are also required for optimal growth in four of the tested conditions. Our results validate the yeast gene-deletion collection as a valuable resource for functional genomics.
引用
收藏
页码:387 / 391
页数:5
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