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一种由HIV编码的反义长链非编码RNA通过表观遗传调控病毒转录。

An HIV-encoded antisense long noncoding RNA epigenetically regulates viral transcription.

作者信息

Saayman Sheena, Ackley Amanda, Turner Anne-Marie W, Famiglietti Marylinda, Bosque Alberto, Clemson Matthew, Planelles Vicente, Morris Kevin V

机构信息

Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, USA.

Department of Pathology, University of Utah, Salt Lake City, Utah, USA.

出版信息

Mol Ther. 2014 Jun;22(6):1164-1175. doi: 10.1038/mt.2014.29. Epub 2014 Feb 28.

Abstract

The abundance of long noncoding RNAs (lncRNAs) and their wide range of functional roles in human cells are fast becoming realized. Importantly, lncRNAs have been identified as epigenetic modulators and consequently play a pivotal role in the regulation of gene expression. A human immunodeficiency virus-encoded antisense RNA transcript has recently been reported and we sought to characterize this RNA and determine its potential role in viral transcription regulation. The intrinsic properties of this human immunodeficiency virus-expressed lncRNA were characterized and the data presented here suggest that it functions as an epigenetic brake to modulate viral transcription. Suppression of this long antisense transcript with small single-stranded antisense RNAs resulted in the activation of viral gene expression. This lncRNA was found to localize to the 5' long-term repeats (LTR) and to usurp components of endogenous cellular pathways that are involved in lncRNA directed epigenetic gene silencing. Collectively, we find that this viral expressed antisense lncRNA is involved in modulating human immunodeficiency virus gene expression and that this regulatory effect is due to an alteration in the epigenetic landscape at the viral promoter.

摘要

人们很快就认识到长链非编码RNA(lncRNAs)在人类细胞中的丰富性及其广泛的功能作用。重要的是,lncRNAs已被确定为表观遗传调节剂,因此在基因表达调控中起着关键作用。最近报道了一种人类免疫缺陷病毒编码的反义RNA转录本,我们试图对这种RNA进行表征,并确定其在病毒转录调控中的潜在作用。对这种人类免疫缺陷病毒表达的lncRNA的内在特性进行了表征,此处呈现的数据表明它作为一种表观遗传制动器来调节病毒转录。用小单链反义RNA抑制这种长反义转录本会导致病毒基因表达的激活。发现这种lncRNA定位于5'长期重复序列(LTR),并篡夺参与lncRNA介导的表观遗传基因沉默的内源性细胞途径的成分。总体而言,我们发现这种病毒表达的反义lncRNA参与调节人类免疫缺陷病毒基因表达,并且这种调节作用是由于病毒启动子处表观遗传格局的改变。

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