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MyoD-BAF60c 依赖信号被募集到基于 Brg1 的 SWI/SNF 染色质重塑复合物中。

Signal-dependent incorporation of MyoD-BAF60c into Brg1-based SWI/SNF chromatin-remodelling complex.

机构信息

Muscle Development and Regeneration Program, Sanford-Burnham Institute for Medical Research, La Jolla, CA, USA.

出版信息

EMBO J. 2012 Jan 18;31(2):301-16. doi: 10.1038/emboj.2011.391. Epub 2011 Nov 8.

Abstract

Tissue-specific transcriptional activators initiate differentiation towards specialized cell types by inducing chromatin modifications permissive for transcription at target loci, through the recruitment of SWItch/Sucrose NonFermentable (SWI/SNF) chromatin-remodelling complex. However, the molecular mechanism that regulates SWI/SNF nuclear distribution in response to differentiation signals is unknown. We show that the muscle determination factor MyoD and the SWI/SNF subunit BAF60c interact on the regulatory elements of MyoD-target genes in myoblasts, prior to activation of transcription. BAF60c facilitates MyoD binding to target genes and marks the chromatin for signal-dependent recruitment of the SWI/SNF core to muscle genes. BAF60c phosphorylation on a conserved threonine by differentiation-activated p38α kinase is the signal that promotes incorporation of MyoD-BAF60c into a Brg1-based SWI/SNF complex, which remodels the chromatin and activates transcription of MyoD-target genes. Our data support an unprecedented two-step model by which pre-assembled BAF60c-MyoD complex directs recruitment of SWI/SNF to muscle loci in response to differentiation cues.

摘要

组织特异性转录激活因子通过募集 SWItch/Sucrose NonFermentable (SWI/SNF) 染色质重塑复合物,在靶基因上诱导允许转录的染色质修饰,从而启动向特化细胞类型的分化。然而,调节 SWI/SNF 核分布以响应分化信号的分子机制尚不清楚。我们表明,在肌母细胞中转录激活之前,肌肉决定因子 MyoD 和 SWI/SNF 亚基 BAF60c 在 MyoD 靶基因的调节元件上相互作用。BAF60c 促进 MyoD 与靶基因结合,并为信号依赖性募集 SWI/SNF 核心到肌肉基因标记染色质。分化激活的 p38α 激酶对保守苏氨酸的磷酸化是促进 MyoD-BAF60c 纳入基于 Brg1 的 SWI/SNF 复合物的信号,该复合物重塑染色质并激活 MyoD 靶基因的转录。我们的数据支持一个前所未有的两步模型,其中预组装的 BAF60c-MyoD 复合物在分化信号的作用下指导 SWI/SNF 向肌肉基因座的募集。

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