Suppr超能文献

一个全面的 Bunyavirales 复制启动子列表揭示了在弹状病毒科中一种独特的启动子结构,与其他病毒家族不同。

A comprehensive list of the Bunyavirales replication promoters reveals a unique promoter structure in Nairoviridae differing from other virus families.

机构信息

School of Agriculture, Utsunomiya University, 350 Mine-machi, Utsunomiya, Tochigi, 321-8505, Japan.

Genome Immunobiology RIKEN Hakubi Research Team, RIKEN Center for Integrative Medical Sciences, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa, 230-0045, Japan.

出版信息

Sci Rep. 2022 Aug 9;12(1):13560. doi: 10.1038/s41598-022-17758-z.

Abstract

Members of the order Bunyavirales infect a wide variety of host species, including plants, animals and humans, and pose a threat to public health. Major families in this order have tri-segmented negative-sense RNA genomes, the 5' and 3' ends of which form complementary strands that serve as a replication promoter. Elucidation of the mechanisms by which viral polymerases recognize the promoter to initiate RNA synthesis is important for understanding viral replication and pathogenesis, and developing antivirals. A list of replication promoter configuration patterns may provide details on the differences in the replication mechanisms among bunyaviruses. By using public sequence data of all known bunyavirus species, we constructed a comprehensive list of the replication promoters comprising 40 nucleotides in both the 5' and 3' ends of the genome that form a specific complementary strand. Among tri-segmented bunyaviruses, members of the family Nairoviridae, including the highly pathogenic Crimean-Congo hemorrhagic fever virus, have evolved a GC-rich promoter structure differing from that of other families. The unique promoter structure might be related to the large genome size of the family Nairoviridae among bunyaviruses, and the large genome architecture might confer pathogenic advantages. The promoter list provided in this report is useful for predicting the virus family-specific replication mechanisms of bunyaviruses.

摘要

布尼亚病毒目成员感染宿主范围广泛,包括植物、动物和人类,对公共卫生构成威胁。该目中的主要科具有三段负义 RNA 基因组,其 5'和 3'末端形成互补链,作为复制启动子。阐明病毒聚合酶如何识别启动子以起始 RNA 合成的机制对于理解病毒复制和发病机制以及开发抗病毒药物非常重要。复制启动子配置模式列表可能提供有关布尼亚病毒之间复制机制差异的详细信息。通过使用所有已知布尼亚病毒物种的公共序列数据,我们构建了一个包含基因组 5'和 3'末端的 40 个核苷酸的复制启动子的综合列表,这些核苷酸形成特定的互补链。在三段式布尼亚病毒中,包括高致病性克里米亚-刚果出血热病毒在内的纳罗病毒科成员已经进化出一种富含 GC 的启动子结构,与其他科不同。独特的启动子结构可能与布尼亚病毒中纳罗病毒科的大型基因组大小有关,而大型基因组结构可能赋予致病优势。本报告提供的启动子列表可用于预测布尼亚病毒的病毒家族特异性复制机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb8/9363447/07e242f330ea/41598_2022_17758_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验