期刊
SCIENCE
卷 344, 期 6180, 页码 208-211出版社
AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1250217
关键词
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资金
- National Human Genome Research Institute [RO1 003317-07]
- Canadian Cancer Society Research Institute [020380]
- Canadian Institute for Health Research [MOP-81340, MOP-79368, MOP-700724]
- Canadian Research Chair
- Charles H. Best Institute
- Belgian National Fund for Scientific Research
- French National Research Agency
- Marie Curie Fellowship
- Leukemia and Lymphoma Society
- Robert A. Welch Foundation
- NIH [GM103504, GM44530]
- Interuniversity Poles of Attraction Program
Genome-wide characterization of the in vivo cellular response to perturbation is fundamental to understanding how cells survive stress. Identifying the proteins and pathways perturbed by small molecules affects biology and medicine by revealing the mechanisms of drug action. We used a yeast chemogenomics platform that quantifies the requirement for each gene for resistance to a compound in vivo to profile 3250 small molecules in a systematic and unbiased manner. We identified 317 compounds that specifically perturb the function of 121 genes and characterized the mechanism of specific compounds. Global analysis revealed that the cellular response to small molecules is limited and described by a network of 45 major chemogenomic signatures. Our results provide a resource for the discovery of functional interactions among genes, chemicals, and biological processes.
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