生物
简编
计算生物学
药物发现
编码
功能(生物学)
酿酒酵母
遗传学
刺蕊草属
基因
生物信息学
医学
历史
考古
传统医学
作者
Timothy R. Hughes,Matthew J. Marton,Allan R. Jones,CJ Roberts,Roland Stoughton,Christopher D. Armour,Holly A. Bennett,Ernest M. Coffey,Hongyue Dai,Yudong D. He,M. Kidd,Amy King,Michael R. Meyer,David Slade,Pek Yee Lum,S. Stepaniants,Daniel Shoemaker,Daniel Gachotte,Kalpana Chakraburtty,Julian A. Simon,Martin Bard,Stephen Friend
出处
期刊:Cell
[Elsevier]
日期:2000-07-01
卷期号:102 (1): 109-126
被引量:2567
标识
DOI:10.1016/s0092-8674(00)00015-5
摘要
Ascertaining the impact of uncharacterized perturbations on the cell is a fundamental problem in biology. Here, we describe how a single assay can be used to monitor hundreds of different cellular functions simultaneously. We constructed a reference database or “compendium” of expression profiles corresponding to 300 diverse mutations and chemical treatments in S. cerevisiae, and we show that the cellular pathways affected can be determined by pattern matching, even among very subtle profiles. The utility of this approach is validated by examining profiles caused by deletions of uncharacterized genes: we identify and experimentally confirm that eight uncharacterized open reading frames encode proteins required for sterol metabolism, cell wall function, mitochondrial respiration, or protein synthesis. We also show that the compendium can be used to characterize pharmacological perturbations by identifying a novel target of the commonly used drug dyclonine.
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