Chen X, Bruening G
Department of Plant Pathology, College of Agricultural and Environmental Sciences, University of California, Davis 95616.
Virology. 1992 Dec;191(2):607-18. doi: 10.1016/0042-6822(92)90236-i.
Cowpea severe mosaic virus (CPSMV) is a member of the comovirus group of messenger-sense RNA viruses with bipartite genomes, of which cowpea mosaic virus (CPMV) is the type member. Full-length copies of CPSMV RNA 1 were cloned in plasmids bearing a bacteriophage T7 promoter. Previously, similar clones of CPSMV RNA 2 had been obtained. A 5'-rUAUUAAAAUUUU sequence is common to RNA 1 and RNA 2. From two RNA 1 clones and four RNA 2 clones we excised non-CPSMV sequences so as to provide templates for in vitro transcripts that have only a single guanylate preceding CPSMV RNA sequences. Transcripts from the most active RNA 1 and RNA 2 clones, when mixed, showed about 5% of the infectivity of unfractionated CPSMV RNAs from virions. The longest, 1858 codon open reading frame of the 5957 nt CPSMV RNA 1 extends from an AUG at nt 257 to a UGA termination codon at nt 5831. The calculated molecular weight of the polyprotein is 208,000. Comparisons with the available amino acid residue (aa) sequence information from the complete CPMV RNA 1 sequence and the partial sequence of red clover mottle virus RNA 1 suggest that CPSMV RNA 1 specifies the expected set of five mature proteins: 32K proteinase cofactor, 58K presumed helicase, VPg 5'-linked protein of the genomic RNAs, 24K proteinase, and 87K presumed polymerase, separated by four cleavage sites. Of the determined and deduced cleavage sites of the three RNA 1 polyproteins, only that at the 24K/87K junction has a distinct aa pair in the CPSMV polyprotein. Of the five proteins, VPg and 87K show the greatest similarity between CPSMV and CPMV, with identities of 68 and 55%, respectively. Published mutational analysis of the CPMV 24K proteinase and alignment of aa sequences from three comoviruses suggest that cysteine-168, histidine-40 and glutamic acid-77 form the catalytic triad of the CPSMV 24K proteinase. Results are discussed in the context of the resistance that some cowpea (Vigna unguiculata) lines exhibit against CPMV but not against CPSMV.
豇豆重花叶病毒(CPSMV)是正义RNA病毒中豇豆花叶病毒组的成员,具有双分体基因组,其中豇豆花叶病毒(CPMV)是该组的典型成员。CPSMV RNA 1的全长拷贝被克隆到带有噬菌体T7启动子的质粒中。此前,已获得CPSMV RNA 2的类似克隆。RNA 1和RNA 2共有一个5'-rUAUUAAAAUUUU序列。我们从两个RNA 1克隆和四个RNA 2克隆中切除了非CPSMV序列,以便为体外转录本提供模板,这些转录本在CPSMV RNA序列之前只有一个鸟苷酸。来自活性最高 的RNA 1和RNA 2克隆的转录本混合后,其感染性约为来自病毒粒子的未分级CPSMV RNA的5%。5957 nt的CPSMV RNA 1最长的1858密码子开放阅读框从第257位的AUG延伸至第5831位的UGA终止密码子。多聚蛋白的计算分子量为208,000。与来自完整CPMV RNA 1序列和红三叶草斑驳病毒RNA 1部分序列的可用氨基酸残基(aa)序列信息进行比较表明,CPSMV RNA 1指定了预期的一组五种成熟蛋白:32K蛋白酶辅因子、58K假定解旋酶、基因组RNA的5'-连接VPg蛋白、24K蛋白酶和87K假定聚合酶,它们由四个切割位点分隔。在三种RNA 1多聚蛋白已确定和推导的切割位点中,只有24K/87K连接处的切割位点在CPSMV多聚蛋白中有独特的aa对。在这五种蛋白中,VPg和87K在CPSMV和CPMV之间显示出最大的相似性,同一性分别为68%和55%。已发表的对CPMV 24K蛋白酶的突变分析以及来自三种豇豆花叶病毒的aa序列比对表明,半胱氨酸-168(Cys-168)、组氨酸-40(His-40)和谷氨酸-77(Glu-77)构成了CPSMV 24K蛋白酶的催化三联体。将结合一些豇豆(Vigna unguiculata)品系对CPMV有抗性但对CPSMV没有抗性的情况对结果进行讨论。