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RNA聚合酶II对丁型肝炎病毒RNA的转录

Transcription of hepatitis delta virus RNA by RNA polymerase II.

作者信息

Chang Jinhong, Nie Xingcao, Chang Ho Eun, Han Ziying, Taylor John

机构信息

Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111-2497, USA.

出版信息

J Virol. 2008 Feb;82(3):1118-27. doi: 10.1128/JVI.01758-07. Epub 2007 Nov 21.

Abstract

Previous studies have indicated that the replication of the RNA genome of hepatitis delta virus (HDV) involves redirection of RNA polymerase II (Pol II), a host enzyme that normally uses DNA as a template. However, there has been some controversy about whether in one part of this HDV RNA transcription, a polymerase other than Pol II is involved. The present study applied a recently described cell system (293-HDV) of tetracycline-inducible HDV RNA replication to provide new data regarding the involvement of host polymerases in HDV transcription. The data generated with a nuclear run-on assay demonstrated that synthesis not only of genomic RNA but also of its complement, the antigenome, could be inhibited by low concentrations of amanitin specific for Pol II transcription. Subsequent studies used immunoprecipitation and rate-zonal sedimentation of nuclear extracts together with double immunostaining of 293-HDV cells, in order to examine the associations between Pol II and HDV RNAs, as well as the small delta antigen, an HDV-encoded protein known to be essential for replication. Findings include evidence that HDV replication is somehow able to direct the available delta antigen to sites in the nucleoplasm, almost exclusively colocalized with Pol II in what others have described as transcription factories.

摘要

先前的研究表明,丁型肝炎病毒(HDV)的RNA基因组复制涉及RNA聚合酶II(Pol II)的重定向,Pol II是一种通常以DNA为模板的宿主酶。然而,关于在HDV RNA转录的这一部分中是否涉及Pol II以外的聚合酶,一直存在一些争议。本研究应用了最近描述的四环素诱导型HDV RNA复制细胞系统(293-HDV),以提供关于宿主聚合酶参与HDV转录的新数据。通过核转录分析产生的数据表明,低浓度的特异性针对Pol II转录的鹅膏菌素不仅可以抑制基因组RNA的合成,还可以抑制其互补物抗原基因组的合成。随后的研究使用核提取物的免疫沉淀和速率区带沉降,以及对293-HDV细胞进行双重免疫染色,以研究Pol II与HDV RNA之间的关联,以及小δ抗原,一种已知对复制至关重要的HDV编码蛋白。研究结果包括证据表明,HDV复制能够以某种方式将可用的δ抗原引导至核质中的位点,几乎完全与Pol II共定位于其他人所描述的转录工厂中。

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