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首页> 外文期刊>Nucleic Acids Research >Acetylation increases access of remodelling complexes to their nucleosome targets to enhance initiation of V(D)J recombination
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Acetylation increases access of remodelling complexes to their nucleosome targets to enhance initiation of V(D)J recombination

机译:乙酰化增加了重塑复合物进入其核小体靶标的途径,从而增强了V(D)J重组的启动

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摘要

Targeted chromatin remodelling is essential for many nuclear processes, including the regulation of V(D)J recombination. ATP-dependent nucleosome remodelling complexes are important players in this process whose activity must be tightly regulated. We show here that histone acetylation regulates nucleosome remodelling complex activity to boost RAG cutting during the initiation of V(D)J recombination. RAG cutting requires nucleosome mobilization from recombination signal sequences. Histone acetylation does not stimulate nucleosome mobilization per se by CHRAC, ACF or their catalytic subunit, ISWI. Instead, we find the more open structure of acetylated chromatin regulates the ability of nucleosome remodelling complexes to access their nucleosome templates. We also find that bromodomain/acetylated histone tail interactions can contribute to this targeting at limited concentrations of remodelling complex. We therefore propose that the changes in higher order chromatin structure associated with histone acetylation contribute to the correct targeting of nucleosome remodelling complexes and this is a novel way in which histone acetylation can modulate remodelling complex activity.
机译:靶向染色质重塑对于许多核过程至关重要,包括V(D)J重组的调控。 ATP依赖的核小体重塑复合物是此过程中的重要参与者,必须严格调节其活性。我们在这里显示,组蛋白乙酰化调节核小体重塑复杂的活动,以在V(D)J重组的启动过程中增强RAG切割。 RAG切割需要从重组信号序列中动员核小体。组蛋白乙酰化本身不会通过CHRAC,ACF或其催化亚基ISWI本身刺激核小体动员。相反,我们发现乙酰化染色质的更开放的结构调节了核小体重构复合物访问其核小体模板的能力。我们还发现,溴结构域/乙酰化的组蛋白尾巴相互作用可在有限浓度的重塑复合物中促进这种靶向。因此,我们提出,与组蛋白乙酰化相关的高级染色质结构的改变有助于核小体重塑复合物的正确靶向,这是组蛋白乙酰化可调节重塑复合物活性的新途径。

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