首页> 外文期刊>Molecular and Cellular Biology >BRG1 and BRM Chromatin-Remodeling Complexes Regulate the Hypoxia Response by Acting as Coactivators for a Subset of Hypoxia-Inducible Transcription Factor Target Genes
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BRG1 and BRM Chromatin-Remodeling Complexes Regulate the Hypoxia Response by Acting as Coactivators for a Subset of Hypoxia-Inducible Transcription Factor Target Genes

机译:BRG1和BRM染色质重塑复合物通过作为缺氧诱导转录因子靶基因亚集的共激活物来调节缺氧反应。

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Chromatin remodeling is an active process, which represses or enables the access of transcription machinery to genes in response to external stimuli, including hypoxia. However, in hypoxia, the specific requirement, as well as the molecular mechanism by which the chromatin-remodeling complexes regulate gene expression, remains unclear. In this study, we report that the Brahma (BRM) and Brahma-related gene 1 (BRG1) ATPase-containing SWI/SNF chromatin-remodeling complexes promote the expression of the hypoxia-inducible transcription factor 1α (HIF1α) and HIF2α genes and also promote hypoxic induction of a subset of HIF1 and HIF2 target genes. We show that BRG1 or BRM knockdown in Hep3B and RCC4T cells reduces hypoxic induction of HIF target genes, while reexpression of BRG1 or BRM in BRG1/BRM-deficient SW13 cells increases HIF target gene activation. Mechanistically, HIF1 and HIF2 increase the hypoxic induction of HIF target genes by recruiting BRG1 complexes to HIF target gene promoters, which promotes nucleosome remodeling of HIF target gene promoters in a BRG1 ATPase-dependent manner. Importantly, we found that the function of BRG1 complexes in hypoxic SW13 and RCC4T cells is dictated by the HIF-mediated hypoxia response and could be opposite from their function in normoxic SW13 and RCC4T cells.
机译:染色质重塑是一个活跃的过程,可抑制或使转录机制能够响应外部刺激(包括缺氧)而进入基因。然而,在缺氧状态下,染色质重塑复合物调节基因表达的具体要求以及分子机制尚不清楚。在这项研究中,我们报道了梵天(BRM)和梵天相关基因1(BRG1)ATPase包含SWI / SNF染色质重塑复合物可促进缺氧诱导转录因子1α(HIF1α)和HIF2α基因的表达,以及促进缺氧诱导HIF1和HIF2目标基因的子集。我们显示在Hep3B和RCC4T细胞中BRG1或BRM敲低减少了HIF靶基因的低氧诱导,而在BRG1 / BRM缺陷的SW13细胞中BRG1或BRM的重新表达增加了HIF靶基因的激活。从机制上讲,HIF1和HIF2通过将BRG1复合物募集到HIF靶基因启动子上来增加HIF靶基因的低氧诱导作用,从而以BRG1 ATPase依赖性方式促进HIF靶基因启动子的核小体重塑。重要的是,我们发现BRG1复合物在低氧SW13和RCC4T细胞中的功能由HIF介导的缺氧反应所决定,并且可能与其在常氧SW13和RCC4T细胞中的功能相反。

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