Turpen T
Biosource Genetics Corporation, Vacaville, California 95688.
J Gen Virol. 1989 Aug;70 ( Pt 8):1951-60. doi: 10.1099/0022-1317-70-8-1951.
An aphid-transmissible field isolate of potato virus Y, strain MM, was purified from a pepper host and cloned. All but 18 terminal nucleotides of the 9.7 kb genome are apparently contained in two overlapping cDNA clones. The library of cDNA clones is likely to be representative of the viral RNA population present in infected plants because restriction endonuclease maps derived from cloned and uncloned cDNA are colinear, each region of the genome is represented by several independent clones, and nucleic acid sequencing of 5' and 3'-terminal regions revealed small AU-rich non-coding domains with blocks of nucleotide sequence homology between this strain of PVY and three other potyviruses. The efficient application of cDNA cloning techniques to a large positive-stranded RNA virus is described.
从辣椒寄主中纯化并克隆了马铃薯Y病毒田间分离株MM,它可通过蚜虫传播。9.7 kb基因组中除了18个末端核苷酸外,其余部分显然都包含在两个重叠的cDNA克隆中。cDNA克隆文库可能代表了受感染植物中存在的病毒RNA群体,因为来自克隆和未克隆cDNA的限制性内切酶图谱是共线性的,基因组的每个区域都由几个独立的克隆代表,并且5'和3'末端区域的核酸测序揭示了富含AU的小非编码结构域,该PVY毒株与其他三种马铃薯Y病毒之间存在核苷酸序列同源性区域。本文描述了cDNA克隆技术在大型正链RNA病毒中的有效应用。