Jia Hengxia, Gong Peng
Key Laboratory of Special Pathogens and Biosafety, Center for Biosafety Mega-Science, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
University of Chinese Academy of Sciences, Beijing, China.
Front Microbiol. 2019 Aug 22;10:1945. doi: 10.3389/fmicb.2019.01945. eCollection 2019.
The RNA-dependent RNA polymerases (RdRPs) encoded by the RNA viruses are a unique class of nucleic acid polymerases. Each viral RdRP contains a 500-600 residue catalytic module with palm, fingers, and thumb domains forming an encircled human right hand architecture. Seven polymerase catalytic motifs are located in the RdRP palm and fingers domains, comprising the most conserved parts of the RdRP and are responsible for the RNA-only specificity in catalysis. Functional regions are often found fused to the RdRP catalytic module, resulting in a high level of diversity in RdRP global structure and regulatory mechanism. In this review, we surveyed all 46 RdRP-sequence available virus families of the positive-strand RNA viruses listed in the 2018b collection of the International Committee on Virus Taxonomy (ICTV) and chose a total of 49 RdRPs as representatives. By locating hallmark residues in RdRP catalytic motifs and by referencing structural and functional information in the literature, we were able to estimate the N- and C-terminal boundaries of the catalytic module in these RdRPs, which in turn serve as reference points to predict additional functional regions beyond the catalytic module. Interestingly, a large number of virus families may have additional regions fused to the RdRP N-terminus, while only a few of them have such regions on the C-terminal side of the RdRP. The current knowledge on these additional regions, either in three-dimensional (3D) structure or in function, is quite limited. In the five RdRP-structure available virus families in the positive-strand RNA viruses, only the family has the 3D structural information resolved for such regions. Hence, future efforts to solve full-length RdRP structures containing these regions and to dissect the functional contribution of them are necessary to improve the overall understanding of the RdRP proteins as an evolutionarily integrated group, and our analyses here may serve as a guideline for selecting representative RdRP systems in these studies.
RNA病毒编码的RNA依赖性RNA聚合酶(RdRPs)是一类独特的核酸聚合酶。每个病毒RdRP都包含一个由500 - 600个残基组成的催化模块,其手掌、手指和拇指结构域形成环绕的右手结构。七个聚合酶催化基序位于RdRP的手掌和手指结构域,构成了RdRP最保守的部分,并负责催化过程中仅针对RNA的特异性。功能区域常常与RdRP催化模块融合,导致RdRP整体结构和调控机制具有高度多样性。在本综述中,我们调查了国际病毒分类委员会(ICTV)2018b版收录的所有46个具有RdRP序列的正链RNA病毒科,并总共选择了49个RdRPs作为代表。通过定位RdRP催化基序中的标志性残基,并参考文献中的结构和功能信息,我们能够估计这些RdRPs中催化模块的N端和C端边界,这反过来又作为参考点来预测催化模块之外的其他功能区域。有趣的是,大量病毒科可能在RdRP的N端融合了额外的区域,而只有少数病毒科在RdRP的C端有这样的区域。目前关于这些额外区域的三维(3D)结构或功能的知识相当有限。在正链RNA病毒中五个具有RdRP结构的病毒科中,只有 科解析了这些区域的3D结构信息。因此,未来有必要努力解析包含这些区域的全长RdRP结构,并剖析它们的功能贡献,以全面了解作为一个进化整合群体的RdRP蛋白,我们在此的分析可能为这些研究中选择代表性的RdRP系统提供指导。