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核受体共激活因子在过氧化物酶体增殖物激活受体γ介导的脂肪生成和脂肪细胞能量代谢中的作用。

Nuclear Receptor Cofactors in PPARgamma-Mediated Adipogenesis and Adipocyte Energy Metabolism.

机构信息

McArdle Laboratory for Cancer Research, University of Wisconsin, 1400 University Avenue, Madison, WI 53706, USA.

出版信息

PPAR Res. 2007;2007:53843. doi: 10.1155/2007/53843.

Abstract

Transcriptional cofactors are integral to the proper function and regulation of nuclear receptors. Members of the peroxisome proliferator-activated receptor (PPAR) family of nuclear receptors are involved in the regulation of lipid and carbohydrate metabolism. They modulate gene transcription in response to a wide variety of ligands, a process that is mediated by transcriptional coactivators and corepressors. The mechanisms by which these cofactors mediate transcriptional regulation of nuclear receptor function are still being elucidated. The rapidly increasing array of cofactors has brought into focus the need for a clear understanding of how these cofactors interact in ligand- and cell-specific manners. This review highlights the differential effects of the assorted cofactors regulating the transcriptional action of PPARgamma and summarizes the recent advances in understanding the physiological functions of corepressors and coactivators.

摘要

转录共激活因子是核受体正常功能和调节所必需的。过氧化物酶体增殖物激活受体(PPAR)家族的核受体成员参与脂质和碳水化合物代谢的调节。它们通过转录共激活因子和核心抑制因子来响应各种配体调节基因转录。这些共因子介导核受体功能转录调节的机制仍在阐明中。快速增加的共因子系列突出了需要清楚地了解这些共因子如何以配体和细胞特异性的方式相互作用。这篇综述强调了调节 PPARγ转录作用的各种共因子的不同影响,并总结了理解核心抑制因子和共激活因子生理功能的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c257/1783724/91d24a19553b/PPAR2007-53843.001.jpg

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