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Chromatin Remodeling Complex Interacts with ADD1/SREBP1c To Mediate Insulin-Dependent Regulation of Gene Expression

机译:染色质重塑复合物与ADD1 / SREBP1c相互作用以介导胰岛素依赖性基因表达调控。

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摘要

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.
机译:胰岛素通过调节脂质和葡萄糖代谢在全身能量稳态中起关键作用。在脂肪和肝组织中,ADD1 / SREBP1c是介导胰岛素依赖性基因表达调控的关键转录因子。尽管已经对ADD1 / SREBP1c的转录和蛋白水解激活进行了深入研究,但尚不清楚胰岛素在染色质水平上用ADD1 / SREBP1c调节其靶基因表达的机制。在这里,我们揭示了SWI / SNF染色质重塑因子与ADD1 / SREBP1c相互作用并积极调节胰岛素依赖性基因的表达。胰岛素增强了SWI / SNF染色质重塑因子向其靶基因启动子的募集,伴随着染色质结构以及基因表达的变化。此外,BAF155 / SRG3(SWI / SNF复合体的组成部分)的体内过表达大大促进了胰岛素靶基因的表达和胰岛素敏感性。两者合计,我们的结果表明SWI / SNF染色质重塑复合物不仅通过与ADD1 / SREBP1c相互作用在体内赋予胰岛素依赖性基因表达,而且还赋予体内胰岛素敏感性。

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