Functional discovery via a compendium of expression profiles

被引:1925
作者
Hughes, TR
Marton, MJ
Jones, AR
Roberts, CJ
Stoughton, R
Armour, CD
Bennett, HA
Coffey, E
Dai, HY
He, YDD
Kidd, MJ
King, AM
Meyer, MR
Slade, D
Lum, PY
Stepaniants, SB
Shoemaker, DD
Gachotte, D
Chakraburtty, K
Simon, J
Bard, M
Friend, SH
机构
[1] Rosetta Inpharmat Inc, Kirkland, WA 98034 USA
[2] Indiana Univ Purdue Univ, Dept Biol, Indianapolis, IN 46202 USA
[3] Med Coll Wisconsin, Dept Biochem, Milwaukee, WI 53226 USA
[4] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
关键词
D O I
10.1016/S0092-8674(00)00015-5
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
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.
引用
收藏
页码:109 / 126
页数:18
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