Osman Toba A M, Coutts Robert H A, Buck Kenneth W
Division of Biology, Faculty of Natural Sciences, Sir Alexander Fleming Building, Imperial College London, London SW7 2AZ, United Kingdom.
J Virol. 2006 Nov;80(21):10743-51. doi: 10.1128/JVI.01050-06. Epub 2006 Aug 23.
Cereal yellow dwarf virus (CYDV) RNA has a 5'-terminal genome-linked protein (VPg). We have expressed the VPg region of the CYDV genome in bacteria and used the purified protein (bVPg) to raise an antiserum which was able to detect free VPg in extracts of CYDV-infected oat plants. A template-dependent RNA-dependent RNA polymerase (RdRp) has been produced from a CYDV membrane-bound RNA polymerase by treatment with BAL 31 nuclease. The RdRp was template specific, being able to utilize templates from CYDV plus- and minus-strand RNAs but not those of three unrelated viruses, Red clover necrotic mosaic virus, Cucumber mosaic virus, and Tobacco mosaic virus. RNA synthesis catalyzed by the RdRp required a 3'-terminal GU sequence and the presence of bVPg. Additionally, synthesis of minus-strand RNA on a plus-strand RNA template required the presence of a putative stem-loop structure near the 3' terminus of CYDV RNA. The base-paired stem, a single-nucleotide (A) bulge in the stem, and the sequence of a tetraloop were all required for the template activity. Evidence was produced showing that minus-strand synthesis in vitro was initiated by priming by bVPg at the 3' end of the template. The data are consistent with a model in which the RdRp binds to the stem-loop structure which positions the active site to recognize the 3'-terminal GU sequence for initiation of RNA synthesis by the addition of an A residue to VPg.
谷类黄矮病毒(CYDV)RNA具有一个5'-末端基因组连接蛋白(VPg)。我们已在细菌中表达了CYDV基因组的VPg区域,并使用纯化的蛋白(bVPg)制备了一种抗血清,该抗血清能够检测CYDV感染的燕麦植物提取物中的游离VPg。通过用BAL 31核酸酶处理,从CYDV膜结合RNA聚合酶产生了一种模板依赖性RNA依赖RNA聚合酶(RdRp)。该RdRp具有模板特异性,能够利用CYDV正链和负链RNA的模板,但不能利用三种无关病毒——红三叶草坏死花叶病毒、黄瓜花叶病毒和烟草花叶病毒的模板。由RdRp催化的RNA合成需要一个3'-末端GU序列和bVPg的存在。此外,在正链RNA模板上合成负链RNA需要在CYDV RNA 3'末端附近存在一个推定的茎环结构。碱基配对的茎、茎中的一个单核苷酸(A)凸起以及一个四环的序列对于模板活性都是必需的。有证据表明,体外负链合成是由bVPg在模板3'末端引发的。这些数据与一个模型一致,即RdRp与茎环结构结合,该结构将活性位点定位以识别3'-末端GU序列,从而通过向VPg添加一个A残基来启动RNA合成。