{"title":"驱动病毒进化的 APOBEC3 家族蛋白","authors":"Michael Jonathan, Terumasa Ikeda","doi":"10.3389/fviro.2023.1332010","DOIUrl":null,"url":null,"abstract":"<p>The apolipoprotein B mRNA editing enzyme catalytic polypeptide-like (APOBEC) family consists of cytosine deaminases implicated in diverse and important biological functions. APOBEC3 (A3) proteins belong to the APOBEC/AID family, and they catalyze the deamination of cytosine to uracil in single-stranded DNA and, to a lesser extent, in RNA substrates. In humans, seven <italic>A3</italic> genes have been identified (<italic>A3A</italic>, <italic>A3B</italic>, <italic>A3C</italic>, <italic>A3D</italic>, <italic>A3F</italic>, <italic>A3G</italic>, and <italic>A3H</italic>). The introduction of lethal G-to-A or C-to-U mutations into certain viral genomes leads to virus inactivation. However, the mutagenic capability of A3 proteins could serve as a source of mutations to drive virus evolution. Therefore, recent studies have implied the role of A3 proteins in aiding the evolution of viruses, conferring them with severe manifestations such as drug resistance and/or immune evasion. In this review, we discuss in depth the interactions of A3 proteins with viruses that infect humans and our self-proteins.</p>","PeriodicalId":73114,"journal":{"name":"Frontiers in virology","volume":"12 1","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2023-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"APOBEC3 family proteins as drivers of virus evolution\",\"authors\":\"Michael Jonathan, Terumasa Ikeda\",\"doi\":\"10.3389/fviro.2023.1332010\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The apolipoprotein B mRNA editing enzyme catalytic polypeptide-like (APOBEC) family consists of cytosine deaminases implicated in diverse and important biological functions. APOBEC3 (A3) proteins belong to the APOBEC/AID family, and they catalyze the deamination of cytosine to uracil in single-stranded DNA and, to a lesser extent, in RNA substrates. In humans, seven <italic>A3</italic> genes have been identified (<italic>A3A</italic>, <italic>A3B</italic>, <italic>A3C</italic>, <italic>A3D</italic>, <italic>A3F</italic>, <italic>A3G</italic>, and <italic>A3H</italic>). The introduction of lethal G-to-A or C-to-U mutations into certain viral genomes leads to virus inactivation. However, the mutagenic capability of A3 proteins could serve as a source of mutations to drive virus evolution. Therefore, recent studies have implied the role of A3 proteins in aiding the evolution of viruses, conferring them with severe manifestations such as drug resistance and/or immune evasion. In this review, we discuss in depth the interactions of A3 proteins with viruses that infect humans and our self-proteins.</p>\",\"PeriodicalId\":73114,\"journal\":{\"name\":\"Frontiers in virology\",\"volume\":\"12 1\",\"pages\":\"\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2023-12-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in virology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3389/fviro.2023.1332010\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"VIROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in virology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fviro.2023.1332010","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"VIROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
载脂蛋白 B mRNA 编辑酶催化多肽样(APOBEC)家族由胞嘧啶脱氨酶组成,涉及多种重要的生物学功能。APOBEC3(A3)蛋白属于 APOBEC/AID 家族,它们催化单链 DNA 中的胞嘧啶脱氨为尿嘧啶,其次也催化 RNA 底物中的胞嘧啶脱氨为尿嘧啶。在人类中,已经发现了 7 个 A3 基因(A3A、A3B、A3C、A3D、A3F、A3G 和 A3H)。在某些病毒基因组中引入 G 到 A 或 C 到 U 的致命突变会导致病毒失活。然而,A3 蛋白的诱变能力可能成为推动病毒进化的突变源。因此,最近的研究暗示 A3 蛋白在帮助病毒进化中的作用,赋予病毒严重的表现,如耐药性和/或免疫逃避。在这篇综述中,我们将深入讨论 A3 蛋白与感染人类的病毒以及我们自身蛋白之间的相互作用。
APOBEC3 family proteins as drivers of virus evolution
The apolipoprotein B mRNA editing enzyme catalytic polypeptide-like (APOBEC) family consists of cytosine deaminases implicated in diverse and important biological functions. APOBEC3 (A3) proteins belong to the APOBEC/AID family, and they catalyze the deamination of cytosine to uracil in single-stranded DNA and, to a lesser extent, in RNA substrates. In humans, seven A3 genes have been identified (A3A, A3B, A3C, A3D, A3F, A3G, and A3H). The introduction of lethal G-to-A or C-to-U mutations into certain viral genomes leads to virus inactivation. However, the mutagenic capability of A3 proteins could serve as a source of mutations to drive virus evolution. Therefore, recent studies have implied the role of A3 proteins in aiding the evolution of viruses, conferring them with severe manifestations such as drug resistance and/or immune evasion. In this review, we discuss in depth the interactions of A3 proteins with viruses that infect humans and our self-proteins.