Sopko Richelle, Huang Dongqing, Preston Nicolle, Chua Gordon, Papp Balázs, Kafadar Kimberly, Snyder Mike, Oliver Stephen G, Cyert Martha, Hughes Timothy R, Boone Charles, Andrews Brenda
Department of Medical Genetics and Microbiology, University of Toronto, 1 King's College Circle, Toronto, Ontario M5S 1A8, Canada.
Mol Cell. 2006 Feb 3;21(3):319-30. doi: 10.1016/j.molcel.2005.12.011.
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 (pho85Delta). 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.
许多疾病状态是由基因过表达导致的,通常发生在特定的基因背景下。为了系统地探究基因过表达的表型,我们构建了一个包含5280个酵母菌株的阵列,每个菌株都含有一个酿酒酵母基因的可诱导拷贝,覆盖了基因组的80%以上。大约15%的过表达基因(769个)降低了生长速率。这个基因集在细胞周期调控基因、信号分子和转录因子方面富集。大多数毒性基因的过表达导致的表型不同于已知的缺失突变体表型,这表明过表达表型通常反映了一种特定的调节失衡,而不是蛋白质复合物化学计量的破坏。在细胞周期蛋白依赖性激酶突变体(pho85Delta)的背景下也检测了全局过表达效应。所得的基因集在Pho85p靶标方面富集,并鉴定出酵母钙调神经磷酸酶反应性转录因子Crz1p为底物。这种方法的大规模应用应该为识别由特定信号通路调控的靶分子提供一种策略。