Yeh S D, Jan F J, Chiang C H, Doong T J, Chen M C, Chung P H, Bau H J
Department of Plant Pathology, National Chung Hsing University, Taichung, Taiwan, Republic of China.
J Gen Virol. 1992 Oct;73 ( Pt 10):2531-41. doi: 10.1099/0022-1317-73-10-2531.
The complete nucleotide sequence of the RNA genome of papaya ringspot virus (PRSV) was determined from four overlapping cDNA clones and by direct sequencing of viral RNA. The genomic RNA is 10326 nucleotides in length, excluding the poly(A) tract, and contains one large open reading frame that starts at nucleotide positions 86 to 88 and ends at positions 10118 to 10120, encoding a polyprotein of 3344 amino acids. The highly conserved sequence AAAUAAAANANCUCAACACAACAUA at the 5' end of the RNA of PRSV and those of the other five reported potyviruses shows 80% similarity, suggesting that this region may play a common important role for potyvirus replication. Two cleavage sites of the polyprotein were determined by amino acid sequencing of the N termini of helper component (HC-Pro, amorphous inclusion) and cylindrical inclusion (CI) proteins. Other cleavage sites were predicted by analogy with the other potyviruses. The genetic organization of PRSV is similar to that of the other potyviruses except that the first protein processed from the N terminus of the polyprotein (NT protein) has an M(r) of 63K, 18K to 34K larger than those of the other potyviruses. The cleavage site for liberating the N terminus of the HC-Pro protein was found at the same location down-stream from the consensus sequence FI(V)VRG as that reported for tobacco vein mottling virus. The NT protein of potyviruses is the most variable and may be considered important for identification of individual potyviruses. The most conserved protein of potyviruses appears to be the NIb protein, the putative polymerase for the replication of the potyviral RNA. The genetic organization of PRSV RNA is tentatively proposed to be VPg-5' leader-63K NT-52K HC-Pro-46K-72K CI-6K-48K NIa-59K NIb-35K coat protein-3' non-coding region-poly(A) tract.
通过四个重叠的 cDNA 克隆以及对病毒 RNA 的直接测序,确定了番木瓜环斑病毒(PRSV)RNA 基因组的完整核苷酸序列。基因组 RNA 长度为 10326 个核苷酸,不包括 poly(A) 尾,包含一个大的开放阅读框,起始于核苷酸位置 86 至 88,终止于位置 10118 至 10120,编码一个由 3344 个氨基酸组成的多聚蛋白。PRSV RNA 5' 端高度保守的序列 AAAUAAAANANCUCAACACAACAUA 与其他五种已报道的马铃薯 Y 病毒属病毒的该序列相似性达 80%,这表明该区域可能对马铃薯 Y 病毒属病毒的复制起着共同的重要作用。通过对辅助成分(HC-Pro,无定形内含体)和柱状内含体(CI)蛋白 N 端的氨基酸测序,确定了多聚蛋白的两个切割位点。其他切割位点则通过与其他马铃薯 Y 病毒属病毒类比预测得出。PRSV 的基因结构与其他马铃薯 Y 病毒属病毒相似,只是从多聚蛋白 N 端加工出的首个蛋白(NT 蛋白)的分子量为 63K,比其他马铃薯 Y 病毒属病毒的该蛋白大 18K 至 34K。发现释放 HC-Pro 蛋白 N 端的切割位点与烟草脉斑驳病毒报道的一致序列 FI(V)VRG 下游的相同位置。马铃薯 Y 病毒属病毒的 NT 蛋白是变化最大的,可能对鉴定单个马铃薯 Y 病毒属病毒很重要。马铃薯 Y 病毒属病毒最保守的蛋白似乎是 NIb 蛋白,它是马铃薯 Y 病毒属病毒 RNA 复制的假定聚合酶。PRSV RNA 的基因结构初步推测为 VPg - 5' 前导序列 - 63K NT - 52K HC-Pro - 46K - 72K CI - 6K - 48K NIa - 59K NIb - 35K 外壳蛋白 - 3' 非编码区 - poly(A) 尾。