Astier T, Mamoun R, Guillemain B, Duplan J F, Parodi A L
Ann Rech Vet. 1978;9(4):643-9.
BLV specific RNA sequences were detected by hybridization to the single stranded DNA copy of the viral RNA in fetal lamb kidney cells infected with bovine leukemia virus (FLK-BLV). The DNA synthesis was carried out in vitro by an endogenous reaction. It was found that uninfected lamb cells do not contain RNA sequences related to the BLV genome, whereas BLV-DNA completely annealed to FLK-BLV RNAs. RNA from FLK-BLV cells contains three species of virus specific RNA which sediment respectively at 35 S, 20--24 S and 12--4 S. In view of their EDTA-sensitive association with ribosomes, viral specific RNA sequences are viral messenger RNAs and their polarity is identical to that of the 70 S viral RNA.
通过与感染牛白血病病毒的胎羊肾细胞(FLK - BLV)中病毒RNA的单链DNA拷贝杂交,检测到BLV特异性RNA序列。DNA合成通过内源性反应在体外进行。发现未感染的羊细胞不含有与BLV基因组相关的RNA序列,而BLV - DNA与FLK - BLV RNA完全退火。来自FLK - BLV细胞的RNA包含三种病毒特异性RNA,它们分别在35S、20 - 24S和12 - 4S沉降。鉴于它们与核糖体的EDTA敏感性结合,病毒特异性RNA序列是病毒信使RNA,其极性与70S病毒RNA的极性相同。