Control of pancreas and liver gene expression by HNF transcription factors

被引:1057
作者
Odom, DT
Zizlsperger, N
Gordon, DB
Bell, GW
Rinaldi, NJ
Murray, HL
Volkert, TL
Schreiber, J
Rolfe, PA
Gifford, DK
Fraenkel, E
Bell, GI
Young, RA
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] MIT, Comp Sci Lab, Cambridge, MA 02139 USA
[4] Univ Chicago, Dept Biochem & Mol Biol, Chicago, IL 60637 USA
[5] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[6] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
关键词
D O I
10.1126/science.1089769
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
The transcriptional regulatory networks that specify and maintain human tissue diversity are largely uncharted. To gain insight into this circuitry, we used chromatin immunoprecipitation combined with promoter microarrays to identify systematically the genes occupied by the transcriptional regulators HNF1alpha, HNF4alpha, and HNF6, together with RNA polymerase II, in human liver and pancreatic islets. We identified tissue-specific regulatory circuits formed by HNF1alpha, HNF4alpha, and HNF6 with other transcription factors, revealing how these factors function as master regulators of hepatocyte and islet transcription. Our results suggest how misregulation of HNF4alpha can contribute to type 2 diabetes.
引用
收藏
页码:1378 / 1381
页数:4
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