Mathews A, Dwyer G, Wylie S, Jones M G
Centre for Legumes in Mediterranean Agriculture (CLIMA), Western Australian State Agricultural Biotechnology Centre, Murdoch University, Australia.
Arch Virol. 1995;140(12):2269-72. doi: 10.1007/BF01323246.
We have cloned and sequenced cDNA transcribed from the 3' 1,239 nucleotides of the genomic RNA of a Western Australian isolate (MI) of bean yellow mosaic potyvirus (BYMV). This sequence contains 246 nucleotides of the NIb (replicase) gene and 819 nucleotides representing the entire coding region of the viral coat protein gene, followed by a 3' non-coding region of 174 nucleotides. The coding region of the coat protein gene is identical in length (273 amino acids) to that already reported for other isolates of this virus. The sequence identities obtained for BYMV-MI and published sequences of BYMV isolates range between 85% and 92% for the coding region of the coat protein and 90% to 98% for the 3' non-coding region. Likewise, the region of the NIb gene sequenced shows 99% and 97% sequence identity in the deduced amino acid and the nucleotide sequences, respectively.
我们已经克隆并测序了从西澳大利亚菜豆黄花叶马铃薯Y病毒(BYMV)分离株(MI)基因组RNA的3'端1239个核苷酸转录而来的cDNA。该序列包含246个核苷酸的NIb(复制酶)基因和819个核苷酸,代表病毒外壳蛋白基因的整个编码区,后面跟着一个174个核苷酸的3'非编码区。外壳蛋白基因的编码区长度(273个氨基酸)与该病毒其他分离株已报道的长度相同。BYMV-MI与已发表的BYMV分离株序列在外壳蛋白编码区的序列同一性为85%至92%,在3'非编码区为90%至98%。同样,所测序的NIb基因区域在推导的氨基酸序列和核苷酸序列中分别显示出99%和97%的序列同一性。