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Sister chromatid cohesion establishment occurs in concert with lagging strand synthesis

机译:姐妹染色单体内聚力的建立与滞后链的合成相一致

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摘要

Cohesion establishment is central to sister chromatid tethering reactions and requires Ctf7/Eco1-dependent acetylation of the cohesin subunit Smc3. Ctf7/Eco1 is essential during S phase, and a number of replication proteins (RFC complexes, PCNA and the DNA helicase Chl1) all play individual roles in sister chromatid cohesion. While the mechanism of cohesion establishment is largely unknown, a popular model is that Ctf7/Eco1 acetylates cohesins encountered by and located in front of the fork. In turn, acetylation is posited both to allow fork passage past cohesin barriers and convert cohesins to a state competent to capture subsequent production of sister chromatids. Here, we report evidence that challenges this pre-replicative cohesion establishment model. Our genetic and biochemical studies link Ctf7/Eco1 to the Okazaki fragment flap endonuclease, Fen1. We further report genetic and biochemical interactions between Fen1 and the cohesion-associated DNA helicase, Chl1. These results raise a new model wherein cohesin deposition and establishment occur in concert with lagging strand-processing events and in the presence of both sister chromatids.
机译:凝聚力的建立对姐妹染色单体束缚反应至关重要,并且需要凝聚素亚基Smc3的Ctf7 / Eco1依赖性乙酰化。 Ctf7 / Eco1在S期必不可少,许多复制蛋白(RFC复合物,PCNA和DNA解旋酶Chl1)在姐妹染色单体内聚中均起着各自的作用。虽然建立内聚力的机制尚不清楚,但一种流行的模型是Ctf7 / Eco1乙酰化前叉所遇到并位于前叉的黏附蛋白。反过来,会发生乙酰化,既可以使叉子穿过黏附素屏障,又可以将黏附素转化为能够捕获后续染色单体的状态。在这里,我们报告的证据挑战了这种复制前的凝聚力建立模型。我们的遗传和生化研究表明Ctf7 / Eco1与Okazaki片段瓣内切核酸酶Fen1相关。我们进一步报告了Fen1与内聚相关DNA解旋酶Chl1之间的遗传和生化相互作用。这些结果提出了一种新模型,其中黏附蛋白的沉积和建立与滞后链加工事件同时存在,并且在两个姐妹染色单体存在下均发生。

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  • 年度 2012
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