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环形内含子长非编码 RNA。

Circular intronic long noncoding RNAs.

机构信息

State Key Laboratory of Molecular Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.

出版信息

Mol Cell. 2013 Sep 26;51(6):792-806. doi: 10.1016/j.molcel.2013.08.017. Epub 2013 Sep 12.

Abstract

We describe the identification and characterization of circular intronic long noncoding RNAs in human cells, which accumulate owing to a failure in debranching. The formation of such circular intronic RNAs (ciRNAs) can be recapitulated using expression vectors, and their processing depends on a consensus motif containing a 7 nt GU-rich element near the 5' splice site and an 11 nt C-rich element close to the branchpoint site. In addition, we show that ciRNAs are abundant in the nucleus and have little enrichment for microRNA target sites. Importantly, knockdown of ciRNAs led to the reduced expression of their parent genes. One abundant such RNA, ci-ankrd52, largely accumulates to its sites of transcription, associates with elongation Pol II machinery, and acts as a positive regulator of Pol II transcription. This study thus suggests a cis-regulatory role of noncoding intronic transcripts on their parent coding genes.

摘要

我们描述了在人类细胞中识别和表征环形内含子长非编码 RNA 的方法,这些 RNA 由于去分支化失败而积累。可以使用表达载体再现这种环形内含子 RNA(ciRNA)的形成,其加工取决于包含靠近 5' 剪接位点的 7 个核苷酸 GU 丰富元件和靠近分支点的 11 个核苷酸 C 丰富元件的共识基序。此外,我们还表明,ciRNA 在核内丰富,并且对 microRNA 靶位点的富集程度较低。重要的是,ciRNA 的敲低导致其亲本基因的表达减少。一种丰富的此类 RNA,ci-ankrd52,主要积累在其转录部位,与延伸 Pol II 机制相关,并作为 Pol II 转录的正调节剂。因此,这项研究表明非编码内含子转录本对其亲本编码基因具有顺式调控作用。

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