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丁型肝炎病毒的分子生物学

The molecular biology of hepatitis delta virus.

作者信息

Lai M M

机构信息

Howard Hughes Medical Institute, University of Southern California School of Medicine, Los Angeles 90033, USA.

出版信息

Annu Rev Biochem. 1995;64:259-86. doi: 10.1146/annurev.bi.64.070195.001355.

Abstract

Hepatitis delta virus (HDV) contains a circular, viroid-like RNA genome, the only animal viral RNA of its kind. It possesses a ribozyme activity, which can autocatalytically cleave and ligate itself. The ribozyme has a unique structural requirement different from other known ribozymes. HDV RNA undergoes RNA-dependent RNA replication via a double rolling circle mechanism, which is probably mediated by cellular RNA polymerase II, utilizing modified cellular transcription machineries. HDV RNA encodes a single protein, hepatitis delta antigen, which is a nuclear, RNA-binding phosphoprotein and required for viral RNA replication. During replication, HDV RNA undergoes a specific RNA editing event to extend its open reading frame and produce a longer, isoprenylated delta antigen, which suppresses RNA replication and initiates viral particle assembly. Ribozyme, cell-mediated RNA-dependent RNA replication, and RNA editing are some of the unique properties and unresolved issues of the molecular biology of HDV.

摘要

丁型肝炎病毒(HDV)含有一个环状、类病毒样的RNA基因组,是此类唯一的动物病毒RNA。它具有核酶活性,能够自我催化切割和连接。该核酶具有与其他已知核酶不同的独特结构要求。HDV RNA通过双滚环机制进行RNA依赖性RNA复制,这可能由细胞RNA聚合酶II介导,利用经过修饰的细胞转录机制。HDV RNA编码一种单一蛋白质,即丁型肝炎抗原,它是一种核内、RNA结合磷蛋白,是病毒RNA复制所必需的。在复制过程中,HDV RNA经历特定的RNA编辑事件,以延长其开放阅读框并产生更长的、异戊二烯化的丁型肝炎抗原,该抗原抑制RNA复制并启动病毒颗粒组装。核酶、细胞介导的RNA依赖性RNA复制以及RNA编辑是HDV分子生物学的一些独特特性和尚未解决的问题。

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