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Inactivation of the budding yeast cohesin loader Scc2 alters gene expression both globally and in response to a single DNA double strand break

机译:萌芽的酵母黏附素装载剂Scc2的失活会改变全局表达以及对单个DNA双链断裂的响应

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摘要

Genome integrity is fundamental for cell survival and cell cycle progression. Important mechanisms for keeping the genome intact are proper sister chromatid segregation, correct gene regulation and efficient repair of damaged DNA. Cohesin and its DNA loader, the Scc2/4 complex have been implicated in all these cellular actions. The gene regulation role has been described in several organisms. In yeast it has been suggested that the proteins in the cohesin network would effect transcription based on its role as insulator. More recently, data are emerging indicating direct roles for gene regulation also in yeast. Here we extend these studies by investigating whether the cohesin loader Scc2 is involved in regulation of gene expression. We performed global gene expression profiling in the absence and presence of DNA damage, in wild type and Scc2 deficient G2/M arrested cells, when it is known that Scc2 is important for DNA double strand break repair and formation of damage induced cohesion. We found that not only the DNA damage specific transcriptional response is distorted after inactivation of Scc2 but also the overall transcription profile. Interestingly, these alterations did not correlate with changes in cohesin binding.
机译:基因组完整性是细胞存活和细胞周期进程的基础。保持基因组完整的重要机制是正确的姐妹染色单体分离,正确的基因调控和对受损DNA的有效修复。粘着蛋白及其DNA装载剂Scc2 / 4复合物已参与所有这些细胞活动。基因调节作用已经在几种生物中描述过。在酵母中,已经提出粘附蛋白网络中的蛋白质将基于其作为绝缘体的作用而影响转录。最近,越来越多的数据表明酵母中基因调控的直接作用。在这里,我们通过研究黏着蛋白加载器Scc2是否参与基因表达的调控来扩展这些研究。当已知Scc2对DNA双链断裂修复和损伤诱导的内聚力形成很重要时,我们在野生型和Scc2缺陷型G2 / M阻滞细胞中不存在和存在DNA损伤的情况下进行了全局基因表达谱分析。我们发现,Scc2失活后,不仅DNA损伤特异性转录反应发生畸变,而且整体转录谱也发生了变化。有趣的是,这些改变与黏着蛋白结合的改变不相关。

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