Tsichlis P N, Coffin J M
Proc Natl Acad Sci U S A. 1979 Jun;76(6):3001-5. doi: 10.1073/pnas.76.6.3001.
The ability of the defective acute leukemia virus of chickens, MC-29, to participate in recombination was investigated by testing the ability of the MC-29 genome to donate sequences to its helper virus. The endogenous virus Rous associated virus O (RAV-O) was used as a helper for MC-29, and its genome was compared by fingerprinting to that of the original RAV-O. In three separate isolates, it was found that the RAV-O used as helper for MC-29 had acquired new sequences near the 3' and 5' ends of its genome. The new 3' proximal sequences resembled the C region found in exogenous but not endogenous avian oncoviruses, and it probably imparted a higher growth rate to the recombinant as compared to RAV-O. One isolate also showed recombination within the env gene. Because we could exclude the possibility that the recombination was with host cell information or with the original helper of MC-29, we conclude that the acquired sequences were derived from the MC-29 genome, and therefore this replication defective virus is not defective in recombination.
通过检测MC-29基因组向其辅助病毒提供序列的能力,研究了鸡的缺陷型急性白血病病毒MC-29参与重组的能力。内源性病毒劳氏相关病毒O(RAV-O)被用作MC-29的辅助病毒,并通过指纹图谱将其基因组与原始RAV-O的基因组进行比较。在三个独立的分离株中,发现用作MC-29辅助病毒的RAV-O在其基因组的3'和5'末端附近获得了新序列。新的3'近端序列类似于在外源而非内源禽肿瘤病毒中发现的C区域,与RAV-O相比,它可能赋予重组体更高的生长速率。一个分离株还显示env基因内发生了重组。因为我们可以排除重组是与宿主细胞信息或与MC-29的原始辅助病毒发生的可能性,所以我们得出结论,获得的序列源自MC-29基因组,因此这种复制缺陷型病毒在重组方面没有缺陷。