Identifying transcription factor functions and targets by phenotypic activation

被引:141
作者
Chua, Gordon
Morris, Quaid D.
Sopko, Richelle
Robinson, Mark D.
Ryan, Owen
Chan, Esther T.
Frey, Brendan J.
Andrews, Brenda J.
Boone, Charles
Hughes, Timothy R.
机构
[1] Univ Toronto, Banting & Best Dept Med Res, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Dept Comp Sci, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Dept Elect & Comp Engn, Toronto, ON M5S 1A8, Canada
[4] Univ Toronto, Dept Med Genet & Microbiol, Toronto, ON M5S 1A8, Canada
关键词
microarray; overexpression; yeast;
D O I
10.1073/pnas.0605140103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mapping transcriptional regulatory networks is difficult because many transcription factors (TFs) are activated only under specific conditions. We describe a generic strategy for identifying genes and pathways induced by individual TFs that does not require knowledge of their normal activation cues. Microarray analysis of 55 yeast TFs that caused a growth phenotype when overexpressed showed that the majority caused increased transcript levels of genes in specific physiological categories, suggesting a mechanism for growth inhibition. Induced genes typically included established targets and genes with consensus promoter motifs, if known, indicating that these data are useful for identifying potential new target genes and binding sites. We identified the sequence 5'-TCACGCAA as a binding sequence for Hms1p, a TF that positively regulates pseudohyphal growth and previously had no known motif. The general strategy outlined here presents a straightforward approach to discovery of TF activities and mapping targets that could be adapted to any organism with transgenic technology.
引用
收藏
页码:12045 / 12050
页数:6
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