Combining functional genomics and chemical biology to identify targets of bioactive compounds

被引:52
|
作者
Ho, Cheuk Hei [1 ,2 ]
Piotrowski, Jeff [3 ]
Dixon, Scott J. [4 ]
Baryshnikoval, Anastasia [1 ,2 ]
Costanzol, Michael [1 ,2 ]
Boone, Charles [1 ,2 ]
机构
[1] Univ Toronto, Banting & Best Dept Med Res, Toronto, ON M55 3E1, Canada
[2] Univ Toronto, Dept Mol Genet, Donnelly Ctr, Toronto, ON M55 3E1, Canada
[3] ASI RIKEN, Mol Ligand Target Team, Wako, Saitama 3510198, Japan
[4] Columbia Univ, Dept Biol Sci, Sherman Fairchild Ctr Life Sci 614A, New York, NY 10027 USA
基金
加拿大自然科学与工程研究理事会;
关键词
MODE-OF-ACTION; CANDIDA-ALBICANS; RNA-INTERFERENCE; DELETION MUTANTS; ESSENTIAL GENES; YEAST; SCREEN; PROTEIN; LIBRARY; IDENTIFICATION;
D O I
10.1016/j.cbpa.2010.10.023
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
Genome sequencing projects have revealed thousands of suspected genes, challenging researchers to develop efficient large-scale functional analysis methodologies. Determining the function of a gene product generally requires a means to alter its function. Genetically tractable model organisms have been widely exploited for the isolation and characterization of activating and inactivating mutations in genes encoding proteins of interest. Chemical genetics represents a complementary approach involving the use of small molecules capable of either inactivating or activating their targets. Saccharomyces cerevisiae has been an important test bed for the development and application of chemical genomic assays aimed at identifying targets and modes of action of known and uncharacterized compounds. Here we review yeast chemical genomic assays strategies for drug target identification.
引用
收藏
页码:66 / 78
页数:13
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