Hughes S H
J Virol. 1982 Jul;43(1):191-200. doi: 10.1128/JVI.43.1.191-200.1982.
Rous-associated virus 0 (RAV-0), an endogenous chicken virus, does not cause disease when inoculated into susceptible domestic chickens. An infectious unintegrated circular RAV-0 DNA was molecularly cloned, and the sequence of the long terminal repeat (LTR) and adjacent segments was determined. The sequence of the LTR was found to be very similar to that of replication-defective endogenous virus EV-1. Like the EV-1 LTR, the RAV-0 LTR is smaller (278 base pairs instead of 330) than the LTRs of the oncogenic members of the avian sarcoma virus-avian leukosis virus group. There is, however, significant homology. The most striking differences are in the U(3) region of the LTR, and in this region there are a series of small segments present in the oncogenic viruses which are absent in RAV-0. These differences in the U(3) region of the LTR could account for the differences in the oncogenic potential of RAV-0 and the avian leukosis viruses. I also compared the regions adjacent to the RAV-0 LTR with the available avian sarcoma virus sequences. A segment of approximately 200 bases to the right of the LTR (toward gag) is almost identical in RAV-0 and the Prague C strain of Rous sarcoma virus. The segment of RAV-0 which lies between the end of the env gene and U(3) is approximately 190 bases in length. Essentially this entire segment is present between env and src in the Schmidt-Ruppin A strain of Rous sarcoma virus. Most of this segment is also present between env and src in Prague C; however, in Prague C there is an apparent deletion of 40 bases in the region adjacent to env. In Schmidt-Ruppin A, but not in Prague C, about half of this segment is also present between src and the LTR. This arrangement has implications for the mechanism by which src was acquired. The region which encoded the gp37 portion of env appears to be very similar in RAV-0 and the Rous sarcoma viruses. However, differences at the very end of env imply that the carboxy termini of RAV-0, Schmidt-Ruppin A, and Prague C gp37s are significantly different. The implications of these observations are considered.
劳氏相关病毒0(RAV-0)是一种内源性鸡病毒,接种到易感家鸡体内时不会引发疾病。一种具有感染性的未整合环状RAV-0 DNA被进行了分子克隆,并测定了长末端重复序列(LTR)及相邻片段的序列。结果发现,RAV-0的LTR序列与复制缺陷型内源性病毒EV-1的序列非常相似。与EV-1的LTR一样,RAV-0的LTR比禽肉瘤病毒-禽白血病病毒组的致癌成员的LTR更小(278个碱基对而非330个)。然而,它们之间存在显著的同源性。最显著的差异存在于LTR的U(3)区域,在该区域,致癌病毒中存在一系列小片段,而RAV-0中则没有。LTR的U(3)区域的这些差异可能解释了RAV-0和禽白血病病毒在致癌潜力上的差异。我还将RAV-0 LTR相邻区域与现有的禽肉瘤病毒序列进行了比较。在RAV-0和劳氏肉瘤病毒布拉格C株中,LTR右侧(朝向gag)约200个碱基的片段几乎完全相同。RAV-0位于env基因末端与U(3)之间的片段长度约为190个碱基。基本上,整个这段序列存在于劳氏肉瘤病毒施密特-鲁平A株的env和src之间。这段序列的大部分也存在于布拉格C株的env和src之间;然而,在布拉格C株中,env相邻区域明显缺失40个碱基。在施密特-鲁平A株中,但不在布拉格C株中,这段序列的大约一半也存在于src和LTR之间。这种排列方式对获得src的机制具有启示意义。编码env的gp37部分的区域在RAV-0和劳氏肉瘤病毒中似乎非常相似。然而,env末端的差异意味着RAV-0、施密特-鲁平A株和布拉格C株的gp37的羧基末端存在显著差异。文中对这些观察结果的意义进行了探讨。