Thal Melissa A, Wasik Brian R, Posto Jessica, Hardy Richard W
Department of Biology, Indiana University, 1001 E. Third Street, Bloomington, IN 47405, USA.
Virology. 2007 Feb 5;358(1):221-32. doi: 10.1016/j.virol.2006.08.022. Epub 2006 Sep 18.
The Sindbis virus (SIN) nonstructural protein nsP4 possesses the RNA-dependent RNA polymerase activity required for the replication of the SIN genome and transcription of a subgenomic mRNA during infection. Isolation of this protein from other viral components of the RNA synthetic complex allowed the characterization of template requirements for nsP4-mediated genome replication. The major findings of this study are: (i) in the absence of other viral proteins nsP4 is capable of copying SIN plus- and minus-strand templates, but does not transcribe subgenomic RNA; (ii) mutations in the 3' conserved sequence element and poly(A) tail of the plus-strand template prevent nsP4-mediated de novo initiation of minus-strand RNA synthesis; (iii) nsP4-dependent terminal addition of nucleotides occurs on template RNA possessing certain mutations in the 3'CSE and polyadenylate tail ; (iv) nsP4 is capable of minus-strand synthesis independent of the sequence at the 5' end of the template; (v) an A-U rich sequence in the 3'CSE represents a binding site for a replicase component, probably nsP4; (vi) plus-strand genomic RNA synthesis is dependent on the 3' end of the minus-strand template. These studies begin to define the specific interactions with the viral RNA templates mediated by individual components of the viral replication complex and suggest a model for ternary complex formation during the initiation of minus-strand RNA synthesis.
辛德毕斯病毒(SIN)的非结构蛋白nsP4具有RNA依赖性RNA聚合酶活性,该活性是SIN基因组复制以及感染期间亚基因组mRNA转录所必需的。从RNA合成复合物的其他病毒成分中分离出这种蛋白质,使得能够对nsP4介导的基因组复制的模板需求进行表征。本研究的主要发现如下:(i)在没有其他病毒蛋白的情况下,nsP4能够复制SIN正链和负链模板,但不能转录亚基因组RNA;(ii)正链模板的3'保守序列元件和聚(A)尾中的突变会阻止nsP4介导的负链RNA合成的从头起始;(iii)在3'CSE和聚腺苷酸尾中具有某些突变的模板RNA上会发生nsP4依赖性的核苷酸末端添加;(iv)nsP4能够独立于模板5'端的序列进行负链合成;(v)3'CSE中富含A-U的序列代表复制酶组分(可能是nsP4)的结合位点;(vi)正链基因组RNA合成依赖于负链模板的3'端。这些研究开始定义病毒复制复合物的各个组分与病毒RNA模板之间的特异性相互作用,并提出了负链RNA合成起始期间三元复合物形成的模型。