Tracy S L, Frenkel M J, Gough K H, Hanna P J, Shukla D D
CSIRO Division of Biomolecular Engineering, Parkville, Victoria, Australia.
Arch Virol. 1992;122(3-4):249-61. doi: 10.1007/BF01317187.
The sequences of the 3' 1019 nucleotides of the genome of an atypical strain of bean yellow mosaic virus (BYMV-S) and of the 3' 1018 nucleotides of the clover yellow vein virus (CYVV-B) genome have been determined. These sequences contain the complete coding region of the viral coat protein followed by a 3' non-coding region of 173 and 178 nucleotides for BYMV-S and CYVV-B, respectively. When the deduced amino acid sequences of the coat protein coding regions were compared, a sequence identity of 77% was found between the two viruses, and optimal alignment of the 3' untranslated regions of BYMV-S and CYVV-B gave a 65% identity. However, the degree of homology of the amino acid sequences of coat proteins of BYMV-S with the published sequences for three other strains of BYMV ranged from 88% to 94%, while the sequence homology of the 3' untranslated regions between the four strains of BYMV ranged between 86% and 95%. Amplified DNA probes corresponding to the 3' non-coding regions of BYMV-S and CYVV-B showed strong hybridization only with the strains of their respective viruses and not with strains of other potyviruses, including pea mosaic virus (PMV). The relatively low sequence identities between the BYMV-S and CYVV-B coat proteins and their 3' non-coding regions, together with the hybridization results, indicate that BYMV, CYVV, and PMV are distinct potyviruses.
已测定了一株非典型菜豆黄花叶病毒(BYMV-S)基因组3′端1019个核苷酸的序列以及三叶草黄脉病毒(CYVV-B)基因组3′端1018个核苷酸的序列。这些序列包含病毒外壳蛋白的完整编码区,随后是BYMV-S和CYVV-B分别为173和178个核苷酸的3′非编码区。当比较外壳蛋白编码区推导的氨基酸序列时,发现两种病毒之间的序列同一性为77%,并且BYMV-S和CYVV-B的3′非翻译区的最佳比对给出了65%的同一性。然而,BYMV-S外壳蛋白的氨基酸序列与其他三株BYMV已发表序列的同源程度在88%至94%之间,而四株BYMV之间3′非翻译区的序列同源性在86%至95%之间。对应于BYMV-S和CYVV-B的3′非编码区的扩增DNA探针仅与各自病毒的毒株显示出强杂交,而不与包括豌豆花叶病毒(PMV)在内的其他马铃薯Y病毒的毒株杂交。BYMV-S和CYVV-B外壳蛋白及其3′非编码区之间相对较低的序列同一性以及杂交结果表明,BYMV、CYVV和PMV是不同的马铃薯Y病毒。