Peebles P T, Strand M, August J T
J Gen Virol. 1978 Sep;40(3):503-10. doi: 10.1099/0022-1317-40-3-503.
Moloney-murine sarcoma virus (S+L- strain of M-MSV) has been nonproductively cloned in murine and non-murine host cells (S+L- cells) and the expression of Moloney leukaemia virus (M-MuLV) 30000 mol. wt. core protein (p30) and envelope glycoprotein (gp69/71) were studied by radioimmunoassay. Antigenic determinants of the M-MuLV p30 were associated with the sarcoma virus genome in these non-productively transformed cell clones studied, while the determinants of M-MuLV gp69/71 were not. The absence of envelope-associated glycoprotein expression in sarcoma virus transformed cells was confirmation of biological studies demonstrating that rescued sarcoma virions acquire envelope-associated properties of host range, neutralization and interference from rescuing helper virus, and further evidence that the M-MuLV gp69/71 sequences have been deleted during the formation of the M-MSV. During the course of these studies, it was also found that S+L- dog cells were releasing into culture supernatant large amounts of the p30 antigenic determinant, apparently as a soluble antigen.
莫洛尼鼠肉瘤病毒(M-MSV的S+L-株)已在鼠类和非鼠类宿主细胞(S+L-细胞)中进行了非生产性克隆,并通过放射免疫测定法研究了莫洛尼白血病病毒(M-MuLV)30000分子量核心蛋白(p30)和包膜糖蛋白(gp69/71)的表达。在这些研究的非生产性转化细胞克隆中,M-MuLV p30的抗原决定簇与肉瘤病毒基因组相关,而M-MuLV gp69/71的抗原决定簇则不然。肉瘤病毒转化细胞中缺乏包膜相关糖蛋白表达,这证实了生物学研究结果,即拯救的肉瘤病毒粒子获得了宿主范围、中和作用以及来自拯救辅助病毒的干扰等包膜相关特性,进一步证明了在M-MSV形成过程中M-MuLV gp69/71序列已被删除。在这些研究过程中,还发现S+L-犬细胞向培养上清液中释放大量p30抗原决定簇,显然是以可溶性抗原的形式。