Johansen E, Rasmussen O F, Heide M, Borkhardt B
Danish Research Service for Plant and Soil Science, Lyngby.
Virus Genes. 1991 Oct;5(4):377-80. doi: 10.1007/BF00271536.
cDNA of pea seed-borne mosaic potyvirus (PSbMV) RNA was synthesized and cloned in E. coli. Four overlapping clones that cover the complete PSbMV genome, except the extreme 5' terminus, were identified by restriction enzyme mapping, hybridization analysis, and partial sequencing. Overlapping cDNA clones covering 1386 nucleotides of the 3' terminus were sequenced. The nucleotide sequence contains one open reading frame (ORF), followed by an untranslated region of 163 nucleotides and a poly(A)-tract. The deduced amino acid sequence was found to include the C-terminus of the predicted RNA-dependent RNA polymerase and the coat protein. A glutamine-alanine dipeptide was identified as a putative 49-kD proteinase cleavage site at the N-terminus of the coat protein.
豌豆种传花叶马铃薯Y病毒(PSbMV)RNA的互补DNA(cDNA)被合成并克隆到大肠杆菌中。通过限制性内切酶图谱分析、杂交分析和部分测序,鉴定出四个重叠克隆,它们覆盖了完整的PSbMV基因组,但不包括最末端的5'端。对覆盖3'端1386个核苷酸的重叠cDNA克隆进行了测序。核苷酸序列包含一个开放阅读框(ORF),后面是一个163个核苷酸的非翻译区和一个聚腺苷酸尾。推导的氨基酸序列被发现包括预测的依赖RNA的RNA聚合酶的C末端和外壳蛋白。谷氨酰胺-丙氨酸二肽被鉴定为外壳蛋白N末端假定的49-kD蛋白酶切割位点。