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Single-molecule imaging reveals control of parental histone recycling by free histones during DNA replication

机译:单分子成像显示在DNA复制期间通过自由组蛋白的父母组蛋白再循环的控制

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During replication, nucleosomes are disrupted ahead of the replication fork, followed by their reassembly on daughter strands from the pool of recycled parental and new histones. However, because no previous studies have managed to capture the moment that replication forks encounter nucleosomes, the mechanism of recycling has remained unclear. Here, through real-time single-molecule visualization of replication fork progression in Xenopus egg extracts, we determine explicitly the outcome of fork collisions with nucleosomes. Most of the parental histones are evicted from the DNA, with histone recycling, nucleosome sliding, and replication fork stalling also occurring but at lower frequencies. Critically, we find that local histone recycling becomes dominant upon depletion of endogenous histones from extracts, revealing that free histone concentration is a key modulator of parental histone dynamics at the replication fork. The mechanistic details revealed by these studies have major implications for our understanding of epigenetic inheritance.
机译:在复制期间,核体在复制叉之前被破坏,然后在来自再生父母和新的组蛋白池中的女儿股票上的重新组装。然而,由于没有先前的研究已经设法捕获复制叉遇到核心的那一刻,回收的机制仍不清楚。这里,通过实时单分子可视化卵泛蛋蛋提取物中的复制叉进展,我们明确地确定了与核体的叉碰撞的结果。大多数父母组蛋白被从DNA驱逐,并且也存在组蛋白再循环,核心的滑动和复制叉分流,而是在较低频率下发生。批判性地,我们发现局部组蛋白回收在来自提取物中的内源性组蛋白的耗尽时占主导地位,揭示了自由组蛋白浓度是复制叉上父母组蛋白动力学的关键调节剂。这些研究揭示的机制细节对我们对表观遗传的理解具有重大影响。

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