Mapping pathways and phenotypes by systematic gene overexpression

被引:508
作者
Sopko, R
Huang, DQ
Preston, N
Chua, G
Papp, B
Kafadar, K
Snyder, M
Oliver, SG
Cyert, M
Hughes, TR
Boone, C
Andrews, B
机构
[1] Univ Toronto, Dept Med Genet & Microbiol, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Banting & Best Dept Med Res, Toronto, ON M5G 1L6, Canada
[3] Univ Toronto, Terrence Donnelly Ctr Cellular & Biomol Res, Toronto, ON M5S 3E1, Canada
[4] Univ Manchester, Sch Biol Sci, Fac Life Sci, Manchester M13 9PT, Lancs, England
[5] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06620 USA
[6] Stanford Univ, Dept Biol Sci, Lokey Lab 147, Stanford, CA 94305 USA
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1016/j.molcel.2005.12.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many disease states result from gene overexpression, often in a specific genetic context. To explore gene overexpression phenotypes systematically, we assembled an array of 5280 yeast strains, each containing an inducible copy of an S. cerevisiae gene, covering > 80% of the genome. Approximately 15% of the overexpressed genes (769) reduced growth rate. This gene set was enriched for cell cycle-regulated genes, signaling molecules, and transcription factors. Overexpression of most toxic genes resulted in phenotypes different from known deletion mutant phenotypes, suggesting that overexpression phenotypes usually reflect a specific regulatory imbalance rather than disruption of protein complex stoichiometry. Global overexpression effects were also assayed in the context of a cyclin-dependent kinase mutant (pho85 Delta). The resultant gene set was enriched for Pho85p targets and identified the yeast calcineurin-responsive transcription factor Crz1p as a substrate. Large-scale application of this approach should provide a strategy for identifying target molecules regulated by specific signaling pathways.
引用
收藏
页码:319 / 330
页数:12
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