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Transcription facilitates sister chromatid cohesion on chromosomal arms

机译:转录可促进染色体臂上的姐妹染色单体凝聚

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摘要

Cohesin is a multi-subunit protein complex essential for sister chromatid cohesion, gene expression and DNA damage repair. Although structurally well studied, the underlying determinant of cohesion establishment on chromosomal arms remains enigmatic. Here, we show two populations of functionally distinct cohesin on chromosomal arms using a combination of genomics and single-locus specific DNA-FISH analysis. Chromatin bound cohesin at the loading sites co-localizes with Pds5 and Eso1 resulting in stable cohesion. In contrast, cohesin independent of its loader is unable to maintain cohesion and associates with chromatin in a dynamic manner. Cohesive sites coincide with highly expressed genes and transcription inhibition leads to destabilization of cohesin on chromatin. Furthermore, induction of transcription results in de novo recruitment of cohesive cohesin. Our data suggest that transcription facilitates cohesin loading onto chromosomal arms and is a key determinant of cohesive sites in fission yeast.
机译:粘着蛋白是一种多亚基蛋白复合物,对姐妹染色单体的粘着,基因表达和DNA损伤修复至关重要。尽管在结构上进行了很好的研究,但在染色体臂上建立内聚力的基本决定因素仍然是个谜。在这里,我们使用基因组学和单基因座特异性DNA-FISH分析相结合的方法,在染色体臂上显示了两个功能不同的粘着蛋白种群。染色质结合的黏着蛋白在加载位点与Pds5和Eso1共定位,从而产生稳定的黏着力。相反,独立于其上样剂的粘着蛋白不能维持粘着力,并以动态方式与染色质缔合。内聚位点与高度表达的基因一致,转录抑制导致染色质上内聚肽的不稳定。此外,转录的诱导导致粘性粘着蛋白从头募集。我们的数据表明,转录促进粘着蛋白加载到染色体臂上,并且是裂变酵母中粘着位点的关键决定因素。

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