Pletnev A G, Yamshchikov V F, Blinov V M
FEBS Lett. 1986 May 12;200(2):317-21. doi: 10.1016/0014-5793(86)81160-7.
RNA of a flavivirus, tick-borne encephalitis virus (TBEV; strain Sofjin), was subjected to reverse transcription and the DNA copy was transformed into double-stranded DNA by the action of E. coli DNA-polymerase I (Klenow fragment). This DNA was annealed with plasmid pBR322. The recombinant plasmids were cloned in E. coli K802. The nucleotide sequence of the inserts of the clones, coding for region structural proteins C, M, E and nonstructural protein NS1, was determined by the Maxam-Gilbert method. The genes of structural proteins form a compact cluster. Homology has been studied of the TBEV sequences found with the structures of proteins and RNAs of other flaviviruses, yellow fever virus and West Nile virus, and a high degree of homology was found.
对一种黄病毒——蜱传脑炎病毒(TBEV;索夫金株)的RNA进行逆转录,并通过大肠杆菌DNA聚合酶I(克列诺片段)的作用将DNA拷贝转化为双链DNA。该DNA与质粒pBR322退火。重组质粒在大肠杆菌K802中克隆。通过马克萨姆-吉尔伯特法确定了编码结构蛋白C、M、E和非结构蛋白NS1区域的克隆插入片段的核苷酸序列。结构蛋白的基因形成一个紧密的簇。已研究了所发现的TBEV序列与其他黄病毒、黄热病毒和西尼罗河病毒的蛋白质及RNA结构的同源性,发现具有高度同源性。