Hopkins N, Schindler J, Gottlieb P D
J Virol. 1977 Mar;21(3):1074-8. doi: 10.1128/JVI.21.3.1074-1078.1977.
After co-infection of Sc-1 cells with N- and B-tropic murine leukemia viruses that differ in their XC plaque morphology, Hopkins et al. (1976) obtained viruses, designated XLP-N, that appeared to be recombinants, since they possess the N-tropism of one parent and the XC plaque morphology of the other (the B-tropic virus) parent. Here we present evidence, based on antigenicity and electrophoretic mobility, that some clonal isolates of XLP-N have inherited gp70 gene of their B-tropic virus parent. In addition to providing evidence that XLP-N viruses are recombinants, the fact that an N-tropic virus may apparently possess a gp70 derived from a B-tropic virus provides evidence, which is in agreement with the findings of others (Huang et al., 1973; Krontiris et al., 1973) that the N- or B-tropism of murine leukemia virus does not reside in gp70.
在用具有不同XC噬斑形态的N-嗜性和B-嗜性鼠白血病病毒共同感染Sc-1细胞后,霍普金斯等人(1976年)获得了被命名为XLP-N的病毒,这些病毒似乎是重组体,因为它们具有一个亲本的N-嗜性和另一个(B-嗜性病毒)亲本的XC噬斑形态。在此,我们基于抗原性和电泳迁移率提出证据,表明XLP-N的一些克隆分离株继承了其B-嗜性病毒亲本的gp70基因。除了提供XLP-N病毒是重组体的证据外,一种N-嗜性病毒显然可能拥有源自B-嗜性病毒的gp70这一事实,也提供了与其他人(黄等人,1973年;克龙蒂里斯等人,1973年)的发现一致的证据,即鼠白血病病毒的N-或B-嗜性并不存在于gp70中。