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Erk1/2 Activity Promotes Chromatin Features and RNAPII Phosphorylation at Developmental Promoters in Mouse ESCs

机译:Erk1 / 2活性促进小鼠ESCs中的染色体启动子上的染色质特征和RNAPII磷酸化。

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Erk1/2 activation contributes to mouse ES cell pluripotency. We found a direct role of Erk1/2 in modulating chromatin features required for regulated developmental gene expression. Erk2 binds to specific DNA sequence motifs typically accessed by Jarid2 and PRC2. Negating Erk1/2 activation leads to increased nucleosome occupancy and decreased occupancy of PRC2 and poised RNAPII at Erk2-PRC2-targeted developmental genes. Surprisingly, Erk2-PRC2-targeted genes are specifically devoid of TFIIH, known to phosphorylate RNA polymerase II (RNAPII) at serine-5, giving rise to its initiated form. Erk2 interacts with and phosphorylates RNAPII at its serine 5 residue, which is consistent with the presence of poised RNAPII as a function of Erk1/2 activation. These findings underscore a key role for Erk1/2 activation in promoting the primed status of developmental genes in mouse ES cells and suggest that the transcription complex at developmental genes is different than the complexes formed at other genes, offering alternative pathways of regulation.
机译:Erk1 / 2激活有助于小鼠ES细胞的多能性。我们发现Erk1 / 2在调节染色质功能所需的调控发育基因表达中的直接作用。 Erk2与通常由Jarid2和PRC2访问的特定DNA序列基序结合。在Erk2-PRC2靶向的发育基因处,否定Erk1 / 2激活会导致核小体占有率增加,PRC2和RNAPII平衡占有率降低。出乎意料的是,靶向Erk2-PRC2的基因没有特异的TFIIH,已知该蛋白会在丝氨酸-5处磷酸化RNA聚合酶II(RNAPII),从而产生其起始形式。 Erk2在其丝氨酸5残基处与RNAPII相互作用并使其磷酸化,这与作为Erk1 / 2激活功能的平衡RNAPII的存在是一致的。这些发现强调了Erk1 / 2激活在促进小鼠ES细胞中发育基因的启动状态中的关键作用,并表明发育基因上的转录复合物不同于其他基因上形成的复合物,从而提供了替代的调控途径。

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