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PMID: 17387179 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Extracellular matrix-regulated gene expression requires cooperation of SWI/SNF and transcription factors.

The Journal of biological chemistry ·Vol. 282 ·No. 20 ·2007-05-18 ·Pages 14992-9

Xu R, Spencer VA, Bissell MJ

Abstract

Extracellular cues play crucial roles in the transcriptional regulation of tissue-specific genes, but whether and how these signals lead to chromatin remodeling is not understood and subject to debate. Using chromatin immunoprecipitation assays and mammary-specific genes as models, we show here that extracellular matrix molecules and prolactin cooperate to induce histone acetylation and binding of transcription factors and the SWI/SNF complex to the beta- and gamma-casein promoters. Introduction of a dominant negative Brg1, an ATPase subunit of SWI/SNF complex, significantly reduced both beta- and gamma-casein expression, suggesting that SWI/SNF-dependent chromatin remodeling is required for transcription of mammary-specific genes. Chromatin immunoprecipitation analyses demonstrated that the ATPase activity of SWI/SNF is necessary for recruitment of RNA transcriptional machinery, but not for binding of transcription factors or for histone acetylation. Co-immunoprecipitation analyses showed that the SWI/SNF complex is associated with STAT5, CCAAT/enhancer-binding protein beta, and glucocorticoid receptor. Thus, extracellular matrix- and prolactin-regulated transcription of the mammary-specific casein genes requires the concerted action of chromatin remodeling enzymes and transcription factors.

MeSH Terms
Acetylation Adenosine Triphosphatases/metabolism Animals CCAAT-Enhancer-Binding Protein-beta/metabolism Caseins/biosynthesis Cell Line Chromatin Assembly and Disassembly/physiology Chromatin Immunoprecipitation Chromosomal Proteins, Non-Histone/metabolism DNA Helicases/genetics,metabolism Extracellular Matrix/metabolism Female Genes, Dominant/genetics Histones/metabolism Mammary Glands, Animal/cytology,metabolism Mice Mutation Nuclear Proteins/genetics,metabolism Organ Specificity/physiology Pregnancy Prolactin/metabolism Promoter Regions, Genetic/physiology Protein Binding/physiology Protein Processing, Post-Translational/physiology Receptors, Glucocorticoid/metabolism STAT5 Transcription Factor/metabolism Transcription Factors/genetics,metabolism Transcription, Genetic/physiology
Chemicals
CCAAT-Enhancer-Binding Protein-beta Caseins Chromosomal Proteins, Non-Histone Histones Nuclear Proteins Receptors, Glucocorticoid STAT5 Transcription Factor SWI-SNF-B chromatin-remodeling complex Transcription Factors Prolactin Adenosine Triphosphatases Smarca4 protein, mouse DNA Helicases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Xu Ren
Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.
Spencer Virginia A
Bissell Mina J
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Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2007-05-18
Epub
2007-00-26
Pages
14992-9
Language
English
Region
United States
NLM ID
2985121R
PMCID
PMC2933196
Subset
IM
Grants
NCI NIH HHS · R01 CA057621 · United States
NCI NIH HHS · R01 CA057621-13 · United States
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