Control of Pancreas and Liver Gene Expression by HNF Transcription Factors

Author:

Odom Duncan T.1234,Zizlsperger Nora1234,Gordon D. Benjamin1234,Bell George W.1234,Rinaldi Nicola J.1234,Murray Heather L.1234,Volkert Tom L.1234,Schreiber Jörg1234,Rolfe P. Alexander1234,Gifford David K.1234,Fraenkel Ernest1234,Bell Graeme I.1234,Young Richard A.1234

Affiliation:

1. Whitehead Institute for Biomedical Research, 9 Cambridge Center, Cambridge, MA 02142, USA.

2. Department of Biology, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139, USA.

3. MIT Laboratory of Computer Science, 200 Technology Square, Cambridge, MA 02139, USA.

4. Departments of Biochemistry and Molecular Biology, Medicine, and Human Genetics, University of Chicago, Chicago, IL 60637, USA.

Abstract

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 HNF1α, HNF4α, and HNF6, together with RNA polymerase II, in human liver and pancreatic islets. We identified tissue-specific regulatory circuits formed by HNF1α, HNF4α, 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 HNF4α can contribute to type 2 diabetes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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