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PMID: 10635321 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

An early developmental transcription factor complex that is more stable on nucleosome core particles than on free DNA.

Molecular cell ·Vol. 4 ·No. 6 ·1999-12-00 ·Pages 961-9

Cirillo LA, Zaret KS

Abstract

In vivo footprinting studies have shown that transcription factor binding sites for HNF3 and GATA-4 are occupied on the albumin gene enhancer in embryonic endoderm, prior to the developmental activation of liver gene transcription. We have investigated how these factors can stably occupy silent chromatin. Remarkably, we find that HNF3, but not GATA-4 or a GAL4 control protein, binds far more stably to nucleosome core particles than to free DNA. In the presence of HNF3, GATA-4 binds stably to an HNF3-positioned nucleosome. Histone acetylation does not affect HNF3 binding. This is evidence for stable nucleosome binding by a transcription factor and shows that a winged helix protein is sufficient to initiate the assembly of an enhancer complex on nonacetylated nucleosomes.

MeSH Terms
Animals Binding Sites Chromatin/genetics,metabolism DNA/genetics,metabolism DNA-Binding Proteins/genetics,metabolism Escherichia coli Forkhead Transcription Factors GATA4 Transcription Factor Mice Nucleosomes/genetics,metabolism Trans-Activators/genetics,metabolism Transcription Factors/genetics,metabolism
Chemicals
Chromatin DNA-Binding Proteins FOXI1 protein, human FOXJ1 protein, human Forkhead Transcription Factors GATA4 Transcription Factor Nucleosomes Trans-Activators Transcription Factors DNA
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Cirillo L A
Department of Molecular Biology, Cell Biology, and Biochemistry, Brown University, Providence, Rhode Island 02912, USA.
Zaret K S
Article Info
Journal
Molecular cell
Abbr.
Mol Cell
ISSN
1097-2765
Published
1999-12-00
Pages
961-9
Language
English
Region
United States
NLM ID
9802571
Subset
IM
Grants
NIGMS NIH HHS · GM47903 · United States
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