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A positioned+1 nucleosome enhances promoter-proximal pausing

机译:定位的+1核小体增强启动子近端暂停

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摘要

Chromatin distribution is not uniform along the human genome. In most genes there is a promoter-associated nucleosome free region (NFR) followed by an array of nucleosomes towards the gene body in which the first (+1) nucleosome is strongly positioned. The function of this characteristic chromatin distribution in transcription is not fully understood. Here we show in vivo that the +1 nucleosome plays a role in modulating RNA polymerase II (RNAPII) promoter-proximal pausing. When a +1 nucleosome is strongly positioned, elongating RNAPII has a tendency to stall at the promoter-proximal region, recruits more negative elongation factor (NELF) and produces less mRNA. The nucleosome-induced pause favors pre-mRNA quality control by promoting the addition of the cap to the nascent RNA. Moreover, the uncapped RNAs produced in the absence of a positioned nucleosome are degraded by the 5'-3' exonuclease XRN2. Interestingly, reducing the levels of the chromatin remodeler ISWI factor SNF2H decreases +1 nucleosome positioning and increases RNAPII pause release. This work demonstrates a function for +1 nucleosome in regulation of transcription elongation, pre-mRNA processing and gene expression.
机译:沿人类基因组的染色质分布不均匀。在大多数基因中,有一个与启动子相关的无核小体区域(NFR),其后是一系列朝向第一个(+1)核小体牢固定位的基因体的核小体。这种特征性染色质分布在转录中的功能尚未完全了解。在这里,我们在体内显示+1核小体在调节RNA聚合酶II(RNAPII)启动子近端暂停中起作用。当+1核小体牢固定位时,延伸的RNAPII趋于停在启动子附近区域,募集更多的负延伸因子(NELF)并产生更少的mRNA。核小体诱导的停顿通过促进将帽添加到新生RNA中而有利于mRNA之前的质量控制。此外,在不存在定位核小体的情况下产生的未封端RNA被5'-3'核酸外切酶XRN2降解。有趣的是,降低染色质重塑剂ISWI因子SNF2H的水平可降低+1核小体的定位并增加RNAPII暂停释放。这项工作证明了+1核小体在转录延伸,mRNA前加工和基因表达调控中的功能。

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