Mason W S, Hsu T W, Yeater C, Sabran J L, Mark G E, Kaji A, Taylor J M
J Virol. 1979 Apr;30(1):132-40. doi: 10.1128/JVI.30.1.132-140.1979.
Quail embryo fibroblasts were infected at low multiplicity with avian sarcoma virus, and transformed cells were selected by their ability to form colonies in agar. Five clones that failed to produce focus-forming virus were examined for (i) intactness of the integrated proviral DNA, (ii) intracellular viral RNA production, (iii) intracellular viral antigen production, (iv) production of virus particles, and (v) rescue of a functional src gene and of parental host range determinants by superinfection with Rous-associated virus-60, an avian leukosis virus of subgroup E. Deletions in the integrated viral DNA were apparent in three of the five nonproducer clones. In one clone producing focus-forming virus, analysis of the integrated viral DNA revealed an insertion in the region of the genome that codes for src.
将鹌鹑胚胎成纤维细胞以低感染复数感染禽肉瘤病毒,通过其在琼脂中形成集落的能力筛选转化细胞。检查了五个未能产生致细胞病变病毒的克隆,以确定:(i)整合的前病毒DNA的完整性;(ii)细胞内病毒RNA的产生;(iii)细胞内病毒抗原的产生;(iv)病毒颗粒的产生;以及(v)通过用E亚群禽白血病病毒劳斯相关病毒-60超感染来拯救功能性src基因和亲本宿主范围决定簇。五个无病毒产生克隆中的三个,整合病毒DNA存在明显缺失。在一个产生致细胞病变病毒的克隆中,对整合病毒DNA的分析显示,在基因组中编码src的区域有一个插入。