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一种新兴副粘病毒——索苏加病毒的病毒聚合酶基因内启动子元件2的功能分析

Functional analysis of promoter element 2 within the viral polymerase gene of an emerging paramyxovirus, Sosuga virus.

作者信息

Akter Lipi, Kawasaki Junna, Rakib Tofazzal Md, Okura Takashi, Kato Fumihiro, Kojima Shohei, Oda Kosuke, Matsumoto Yusuke

机构信息

Transboundary Animal Diseases Research Center, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima, Kagoshima, Japan.

Graduate School of Medicine, Chiba University, Chiba, Chiba, Japan.

出版信息

Microbiol Spectr. 2025 Apr 10;13(5):e0053425. doi: 10.1128/spectrum.00534-25.

Abstract

Paramyxovirus genomes carry bipartite promoters at the 3' ends of both their genome and antigenome, thereby initiating RNA synthesis, which requires the viral polymerase to recognize two elements: the primary promoter element 1 (PE1) and the secondary promoter element 2 (PE2). We have previously shown that the antigenomic PE2 (agPE2) in many viruses in the subfamily is located within the coding region of the viral RNA polymerase L gene. Sosuga virus (SOSV), belonging to the subfamily, is highly pathogenic to humans, thus necessitating high-level containment facilities for infectious virus research. The use of a minigenome system permits studies of viral RNA synthesis at lower biosafety levels. Because minigenomes of negative-strand RNA viruses generally comprise only the untranslated regions, agPE2 within the L coding region-such as those found in like SOSV-is typically omitted. However, generating an SOSV minigenome that retains agPE2 led to a pronounced increase in activity, enabling a detailed examination of the role of agPE2 in SOSV replication. In many , the agPE2 not only acts as a promoter but also encodes part of the L protein, resulting in a distinct motif at the C-terminus of the L protein. We have further shown that this motif is preserved even in that no longer contain the agPE2 within the L gene.IMPORTANCEParamyxoviruses are classified into three major subfamilies: , , and . All paramyxovirus genomes and antigenomes possess bipartite promoters, comprising two elements: promoter element 1 (PE1) at the 3' end and promoter element 2 (PE2) located internally. We previously revealed that, in many , the antigenomic PE2 lies within the coding region of the viral RNA polymerase L gene. In this study, we used Sosuga virus, a member of the subfamily, to elucidate the role of antigenomic PE2 in viral replication. Because the PE2 region encodes part of the L protein, its presence leads to a distinctive motif at the C-terminus of L protein. Notably, this motif is conserved in all , including those that do not harbor the antigenomic PE2 within their L gene, indicating its importance in viral propagation.

摘要

副粘病毒基因组在其基因组和反基因组的3'端都带有二分体启动子,从而启动RNA合成,这需要病毒聚合酶识别两个元件:初级启动子元件1(PE1)和次级启动子元件2(PE2)。我们之前已经表明,该亚科中许多病毒的反基因组PE2(agPE2)位于病毒RNA聚合酶L基因的编码区域内。索苏加病毒(SOSV)属于该亚科,对人类具有高度致病性,因此需要高级别的感染性病毒研究 containment设施。使用微型基因组系统可以在较低的生物安全水平下研究病毒RNA合成。由于负链RNA病毒的微型基因组通常仅包含非翻译区域,L编码区域内的agPE2(如在像SOSV这样的病毒中发现的)通常被省略。然而,生成保留agPE2的SOSV微型基因组导致活性显著增加,从而能够详细研究agPE2在SOSV复制中的作用。在许多病毒中,agPE2不仅作为启动子,还编码L蛋白的一部分,导致L蛋白C末端出现独特的基序。我们进一步表明,即使在L基因中不再包含agPE2的病毒中,这个基序也得以保留。

重要性

副粘病毒分为三个主要亚科

、和。所有副粘病毒基因组和反基因组都拥有二分体启动子,由两个元件组成:3'端的启动子元件1(PE1)和位于内部的启动子元件2(PE2)。我们之前揭示,在许多病毒中,反基因组PE2位于病毒RNA聚合酶L基因的编码区域内。在本研究中,我们使用索苏加病毒(该亚科的成员)来阐明反基因组PE2在病毒复制中的作用。由于PE2区域编码L蛋白的一部分,它的存在导致L蛋白C末端出现独特的基序。值得注意的是,这个基序在所有病毒中都保守,包括那些在L基因中不含有反基因组PE2的病毒,表明其在病毒传播中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fa1/12054172/7a9ec74f44de/spectrum.00534-25.f001.jpg

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