Guyatt K J, Proll D F, Menssen A, Davidson A D
Department of Microbiology, Monash University, Clayton, Melbourne, Victoria, Australia.
Arch Virol. 1996;141(7):1231-46. doi: 10.1007/BF01718827.
The complete nucleotide sequence of an Australian strain of bean yellow mosaic virus (BYMV-S) has been determined from cloned viral cDNAs. The BYMV-S genome is 9 547 nucleotides in length excluding a poly(A) tail. Computer analysis of the sequence revealed a single long open reading frame (ORF) of 9168 nucleotides, commencing at position 206 and terminating with UAG at position 9374-6. The ORF potentially encodes a polyprotein of 3056 amino acids with a deduced Mr of 347 409. The 5' and 3' untranslated regions are 205 and 174 nucleotides in length respectively. Alignment of the amino acid sequence of the BYMV-S polyprotein with those of other potyviruses identified nine putative proteolytic cleavage sites. The predicted consensus cleavage site of the BYMV NIa protease was found to differ from that described for other potyviruses. Processing of the BYMV polyprotein at the designated proteolytic cleavage sites would result in a typical potyviral genome arrangement. The amino acid sequences of the putative BYMV encoded proteins were compared to the homologous gene products of twelve individual potyviruses to identify overall and specific regions of amino acid sequence homology.
已从克隆的病毒cDNA中确定了澳大利亚菜豆黄花叶病毒株(BYMV-S)的完整核苷酸序列。BYMV-S基因组长度为9547个核苷酸,不包括聚(A)尾。对该序列的计算机分析揭示了一个9168个核苷酸的单一长开放阅读框(ORF),起始于第206位,终止于第9374 - 6位的UAG。该ORF可能编码一个由3056个氨基酸组成的多蛋白,推导的分子量为347409。5'和3'非翻译区分别为205和174个核苷酸长。将BYMV-S多蛋白的氨基酸序列与其他马铃薯Y病毒的序列进行比对,确定了9个假定的蛋白水解切割位点。发现BYMV NIa蛋白酶的预测共有切割位点与其他马铃薯Y病毒描述的不同。在指定的蛋白水解切割位点对BYMV多蛋白进行加工将导致典型的马铃薯Y病毒基因组排列。将假定的BYMV编码蛋白的氨基酸序列与12种马铃薯Y病毒的同源基因产物进行比较,以确定氨基酸序列同源性的总体和特定区域。