Koonin E V
Institute of Microbiology, U.S.S.R. Academy of Sciences, Moscow.
J Gen Virol. 1991 Sep;72 ( Pt 9):2197-206. doi: 10.1099/0022-1317-72-9-2197.
Representative amino acid sequences of the RNA-dependent RNA polymerases of all groups of positive-strand RNA viruses were aligned hierarchiacally, starting with the most closely related ones. This resulted in delineation of three large supergroups. Within each of the supergroups, the sequences of segments of approximately 300 amino acid residues originating from the central and/or C-terminal portions of the polymerases could be aligned with statistically significant scores. Specific consensus patterns of conserved amino acid residues were derived for each of the supergroups. The composition of the polymerase supergroups was as follows. I. Picorna-, noda-, como-, nepo-, poty-, bymo-, sobemoviruses, and a subset of luteoviruses (beet western yellows virus and potato leafroll virus). II. Carmo-, tombus-, dianthoviruses, another subset of luteoviruses (barley yellow dwarf virus), pestiviruses, hepatitis C virus (HCV), flaviviruses and, unexpectedly, single-stranded RNA bacteriophages. III. Tobamo-, tobra-, hordei-, tricornaviruses, beet yellows virus, alpha-, rubi-, furoviruses, hepatitis E virus (HEV), potex-, carla-, tymoviruses, and apple chlorotic leaf spot virus. An unusual organization was shown for corona- and torovirus polymerases whose N-terminal regions were found to be related to the respective domains of supergroup I, and the C-terminal regions to those of the supergroup III polymerases. The alignments of the three polymerase supergroups were superimposed to produce a comprehensive final alignment encompassing eight distinct conserved motifs. Phylogenetic analysis using three independent methods of three construction confirmed the separation of the positive-strand RNA viral polymerases into three supergroups and revealed some unexpected clusters within the supergroups. These included the grouping of HCV and the pestiviruses with carmoviruses and related plant viruses in super-group II, and the grouping of HEV and rubiviruses with furoviruses in supergroup III.
对所有正链RNA病毒组的RNA依赖性RNA聚合酶的代表性氨基酸序列进行了分层比对,从关系最密切的序列开始。这导致划分出三个大的超群。在每个超群内,源自聚合酶中央和/或C末端部分的约300个氨基酸残基片段的序列可以以具有统计学意义的得分进行比对。为每个超群推导了保守氨基酸残基的特定共有模式。聚合酶超群的组成如下。I. 小RNA病毒科、野田村病毒科、联体病毒科、线虫传多面体病毒科、马铃薯Y病毒科、黄症病毒科、南方菜豆花叶病毒属,以及黄矮病毒属的一个子集(甜菜西方黄化病毒和马铃薯卷叶病毒)。II. 香石竹潜隐病毒科、番茄丛矮病毒科、石竹病毒科,黄矮病毒属的另一个子集(大麦黄矮病毒)、瘟病毒属、丙型肝炎病毒(HCV)、黄病毒属,以及出乎意料的单链RNA噬菌体。III. 烟草花叶病毒属、烟草脆裂病毒属、大麦病毒属、三叶草病毒属、甜菜黄化病毒、甲型病毒属、悬钩子病毒属、真菌传杆状病毒属、戊型肝炎病毒(HEV)、马铃薯X病毒属、花椰菜花叶病毒属、番茄病毒属,以及苹果褪绿叶斑病毒。冠状病毒和圆环病毒聚合酶显示出一种不寻常的结构,其N末端区域与超群I的相应结构域相关,而C末端区域与超群III聚合酶的结构域相关。将三个聚合酶超群的比对结果叠加,以产生一个包含八个不同保守基序的综合最终比对。使用三种独立构建方法的系统发育分析证实了正链RNA病毒聚合酶分为三个超群,并揭示了超群内一些意想不到的聚类。这些聚类包括超群II中HCV和瘟病毒与香石竹潜隐病毒和相关植物病毒的分组,以及超群III中HEV和风疹病毒与真菌传杆状病毒的分组。