Salm S N, Rey M E, French R
Range and Forage Institute, University of the Witwatersrand, Johannesburg, Pretoria, South Africa.
Arch Virol. 1996;141(1):185-95. doi: 10.1007/BF01718600.
The 2094 nucleotides at the 3'-terminus of a South African isolate of ryegrass mosaic virus (RGMV) was cloned and sequenced. Two putative polyprotein cleavage sites were found: Q/L and E/A, both of which are novel in the Potyviridae. The RGMV-SA cDNA was cloned into an expression vector, pUEX, and a fusion protein of 185 kDa was obtained which reacted strongly to anti-RGMV-SA antiserum. Alignment of the predicted amino acid sequence of RGMV-SA with those of other Potyviridae members showed limited identity, indicating that RGMV-SA is a definite and distinct virus.
克隆并测序了黑麦草花叶病毒(RGMV)南非分离株3'端的2094个核苷酸。发现了两个假定的多蛋白切割位点:Q/L和E/A,这两个位点在马铃薯Y病毒科中都是新的。将RGMV-SA cDNA克隆到表达载体pUEX中,获得了一个185 kDa的融合蛋白,该蛋白与抗RGMV-SA抗血清发生强烈反应。RGMV-SA预测氨基酸序列与其他马铃薯Y病毒科成员的序列比对显示同源性有限,表明RGMV-SA是一种确定的独特病毒。