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痘苗病毒中期和晚期启动子元件受TATA结合蛋白作用。

Vaccinia virus intermediate and late promoter elements are targeted by the TATA-binding protein.

作者信息

Knutson Bruce A, Liu Xu, Oh Jaewook, Broyles Steven S

机构信息

Department of Biochemistry, Purdue University, West Lafayette, IN 47907, USA.

出版信息

J Virol. 2006 Jul;80(14):6784-93. doi: 10.1128/JVI.02705-05.

Abstract

Vaccinia virus replicates in the cytoplasm of the host cell and encodes its own RNA polymerase and transcription factors. The proteins that target the poxvirus RNA polymerase to intermediate- and late-class promoters have not been identified. In this study, representatives of the intermediate and late promoters were characterized at the nucleotide level to identify essential motifs. Both intermediate and late viral promoters are shown to have an essential element suggestive of TATA boxes, which are potential targets for the TATA-binding protein (TBP). Several approaches were used to test for TBP requirement in vaccinia virus transcription, including overexpression of TBP, expression of a dominant negative mutant of TBP, RNA interference, and expression of adenovirus E1A protein, which inactivates TBP. In each case, the results support an essential role for TBP in vaccinia virus intermediate- and late-gene transcription. These findings indicate that poxviruses have integrated TBP as a central feature into an otherwise heterologous transcription system. A model for transcriptional switching, in which both intermediate and late promoter elements are targeted by TBP that recruits viral transcription factors to assemble a functional complex on their cognate promoters and a dysfunctional, repressed complex on the other class, is proposed.

摘要

痘苗病毒在宿主细胞的细胞质中复制,并编码自身的RNA聚合酶和转录因子。尚未鉴定出将痘病毒RNA聚合酶靶向中期和晚期启动子的蛋白质。在本研究中,对中期和晚期启动子的代表进行了核苷酸水平的表征,以鉴定必需基序。中期和晚期病毒启动子均显示具有提示TATA框的必需元件,TATA框是TATA结合蛋白(TBP)的潜在靶标。使用了几种方法来测试痘苗病毒转录中对TBP的需求,包括TBP的过表达、TBP显性负突变体的表达、RNA干扰以及腺病毒E1A蛋白的表达,后者可使TBP失活。在每种情况下,结果都支持TBP在痘苗病毒中期和晚期基因转录中起重要作用。这些发现表明痘病毒已将TBP作为核心特征整合到一个原本异源的转录系统中。提出了一种转录转换模型,其中中期和晚期启动子元件均由TBP靶向,TBP招募病毒转录因子以在其同源启动子上组装功能复合物,并在另一类启动子上组装功能失调的、受抑制的复合物。

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