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An embryonic stem cell chromatin remodeling complex esBAF is an essential component of the core pluripotency transcriptional network

机译:胚胎干细胞染色质重塑复合物esBAF是核心多能性转录网络的重要组成部分

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摘要

Distinctive SWI/SNF-like ATP-dependent chromatin remodeling esBAF complexes are indispensable for the maintenance and pluripotency of mouse embryonic stem (ES) cells [Ho L, et al. (2009) Proc Natl Acad Sci USA 10.1073/pnas.0812889106]. To understand the mechanism underlying the roles of these complexes in ES cells, we performed high-resolution genome-wide mapping of the core ATPase subunit, Brg, using ChIP-Seq technology. We find that esBAF, as represented by Brg, binds to genes encoding components of the core ES transcriptional circuitry, including Polycomb group proteins. esBAF colocalizes extensively with transcription factors Oct4, Sox2 and Nanog genome-wide, and shows distinct functional interactions with Oct4 and Sox2 at its target genes. Surprisingly, no significant colocalization of esBAF with PRC2 complexes, represented by Suz12, is observed. Lastly, esBAF colocalizes with Stat3 and Smad1 genome-wide, consistent with a direct and critical role in LIF and BMP signaling for maintaining self-renewal. Taken together, our studies indicate that esBAF is an essential component of the core pluripotency transcriptional network, and might also be a critical component of the LIF and BMP signaling pathways essential for maintenance of self-renewal and pluripotency.
机译:独特的SWI / SNF样ATP依赖的染色质重塑esBAF复合物对于小鼠胚胎干(ES)细胞的维持和多能性是必不可少的[Ho L,et al。 (2009)美国国家科学院院刊10.1073 / pnas.0812889106]。为了了解这些复合物在ES细胞中的作用机理,我们使用ChIP-Seq技术对核心ATPase亚基Brg进行了高分辨率的全基因组定位。我们发现,以Brg为代表的esBAF与编码核心ES转录电路组件(包括Polycomb组蛋白)的基因结合。 esBAF在整个基因组中与转录因子Oct4,Sox2和Nanog广泛共定位,并在其靶基因上显示与Oct4和Sox2的独特功能相互作用。令人惊讶的是,未观察到esBAF与以Suz12为代表的PRC2复合物的显着共定位。最后,esBAF与Stat3和Smad1全基因组共定位,这与在LIF和BMP信号传导中维持自我更新的直接和关键作用一致。两者合计,我们的研究表明,esBAF是核心多能性转录网络的重要组成部分,也可能是维持自我更新和多能性所必需的LIF和BMP信号通路的关键组成部分。

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