Chromatin remodeling complex interacts with ADD1/SREBP1c to mediate insulin-dependent regulation of gene expression

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Insulin plays a critical role in whole-body energy homeostasis by regulating lipid and glucose metabolism. In fat and liver tissues, ADD1/SREBP1c is a key transcription factor to mediate insulin-dependent regulation of gene expression. Although transcriptional and proteolytic activation of ADD1/SREBP1c has been studied intensively, the mechanism by which insulin regulates expression of its target genes with ADD1/SREBP1c at the chromatin level is unclear. Here, we reveal that SWI/SNF chromatin remodeling factors interact with the ADD1/SREBP1c and actively regulate insulin-dependent gene expression. Insulin enhanced recruitment of SWI/SNF chromatin remodeling factors to its target gene promoters with concomitant changes in the chromatin structures as well as gene expression. Furthermore, in vivo overexpression of BAF155/SRG3, a component of the SWI/SNF complex, substantially promoted insulin target gene expression and insulin sensitivity. Taken together, our results suggest that the SWI/SNF chromatin remodeling complexes confer not only insulin-dependent gene expression but also insulin sensitivity in vivo via interaction with ADD1/SREBP1c.
Publisher
AMER SOC MICROBIOLOGY
Issue Date
2007-01
Language
English
Article Type
Article
Keywords

ELEMENT-BINDING PROTEIN-1C; FATTY-ACID SYNTHESIS; PHOSPHOENOLPYRUVATE CARBOXYKINASE GTP; LIPOPROTEIN RECEPTOR GENE; LIVER-X-RECEPTOR; DIABETES-MELLITUS; TRANSCRIPTIONAL ACTIVITY; ADIPOCYTE DETERMINATION; HISTONE METHYLATION; NUCLEAR SREBP-1C

Citation

MOLECULAR AND CELLULAR BIOLOGY, v.27, no.2, pp.438 - 452

ISSN
0270-7306
DOI
10.1128/MCB.00490-06
URI
http://hdl.handle.net/10203/198377
Appears in Collection
MSE-Journal Papers(저널논문)
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