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Linker Histone H1.2 Directs Genome-wide Chromatin Association of the Retinoblastoma Tumor Suppressor Protein and Facilitates Its Function

机译:接头组蛋白H1.2指导视网膜母细胞瘤肿瘤抑制蛋白的全基因组染色质结合并促进其功能

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The retinoblastoma tumor suppressor protein pRb is a master regulator of cellular proliferation, principally through interaction with E2F and regulation of E2F target genes. Here, we describe the H1.2 linker histone as a major pRb interaction partner. We establish that H1.2 and pRb are found in a chromatin-bound complex on diverse E2F target genes. Interrogating the global influence of H1.2 on the genome-wide distribution of pRb indicated that the E2F target genes affected by H1.2 are functionally linked to cell-cycle control, consistent with the ability of H1.2 to hinder cell proliferation and the elevated levels of chromatin-bound H1-pRb complex, which occur in growth-arrested cells. Our results define a network of E2F target genes as susceptible to the regulatory influence of H1.2, where H1.2 augments global association of pRb with chromatin, enhances transcriptional repression by pRb, and facilitates pRb-dependent cell-cycle arrest.
机译:视网膜母细胞瘤肿瘤抑制蛋白pRb是细胞增殖的主要调节剂,主要通过与E2F相互作用和E2F靶基因的调节来实现。在这里,我们将H1.2接头组蛋白描述为主要的pRb相互作用伙伴。我们确定在各种E2F目标基因的染色质结合复合物中发现了H1.2和pRb。询问H1.2对pRb全基因组分布的全球影响表明,受H1.2影响的E2F靶基因在功能上与细胞周期控制相关,与H1.2阻止细胞增殖和染色质结合的H1-pRb复合物水平升高,发生在生长停滞的细胞中。我们的结果定义了一个易受H1.2调控影响的E2F目标基因网络,其中H1.2增强了pRb与染色质的整体结合,增强了pRb的转录抑制,并促进了pRb依赖性细胞周期的阻滞。

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