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鉴定来自乙型肝炎 delta 病毒基因组的 RNA 片段上 ASF/SF2 的结合位点。

Identification of a binding site for ASF/SF2 on an RNA fragment derived from the hepatitis delta virus genome.

机构信息

Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Canada.

出版信息

PLoS One. 2013;8(1):e54832. doi: 10.1371/journal.pone.0054832. Epub 2013 Jan 18.

Abstract

The hepatitis delta virus (HDV) is a small (~1700 nucleotides) RNA pathogen which encodes only one open reading frame. Consequently, HDV is dependent on host proteins to replicate its RNA genome. Recently, we reported that ASF/SF2 binds directly and specifically to an HDV-derived RNA fragment which has RNA polymerase II promoter activity. Here, we localized the binding site of ASF/SF2 on the HDV RNA fragment by performing binding experiments using purified recombinant ASF/SF2 combined with deletion analysis and site-directed mutagenesis. In addition, we investigated the requirement of ASF/SF2 for HDV RNA replication using RNAi-mediated knock-down of ASF/SF2 in 293 cells replicating HDV RNA. Overall, our results indicate that ASF/SF2 binds to a purine-rich region distant from both the previously published initiation site of HDV mRNA transcription and binding site of RNAP II, and suggest that this protein is not involved in HDV replication in the cellular system used.

摘要

乙型肝炎 delta 病毒 (HDV) 是一种小的 (~1700 个核苷酸) RNA 病原体,仅编码一个开放阅读框。因此,HDV 依赖于宿主蛋白来复制其 RNA 基因组。最近,我们报道 ASF/SF2 直接结合并特异性地结合到具有 RNA 聚合酶 II 启动子活性的 HDV 衍生 RNA 片段上。在这里,我们通过使用纯化的重组 ASF/SF2 进行结合实验,结合缺失分析和定点突变,定位了 ASF/SF2 在 HDV RNA 片段上的结合位点。此外,我们使用 RNAi 介导的 ASF/SF2 在复制 HDV RNA 的 293 细胞中敲低,研究了 ASF/SF2 对 HDV RNA 复制的要求。总的来说,我们的结果表明,ASF/SF2 结合到一个嘌呤丰富的区域,远离先前报道的 HDV mRNA 转录起始位点和 RNAP II 结合位点,这表明该蛋白不参与所用细胞系统中的 HDV 复制。

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