Tsichlis P N, Donehower L, Hager G, Zeller N, Malavarca R, Astrin S, Skalka A M
Mol Cell Biol. 1982 Nov;2(11):1331-8. doi: 10.1128/mcb.2.11.1331-1338.1982.
NTRE 7 is an avian retrovirus recombinant of the endogenous nononcogenic Rous-associated virus-0 (RAV-0) and the oncogenic, exogenous, transformation-defective (td) Prague strain of Rous sarcoma virus B (td-PrRSV-B). Oligonucleotide mapping had shown that the recombinant virus is indistinguishable from its RAV-0 parent except for the 3'-end sequences, which were derived from td-PrRSV-B. However, the virus exhibits properties which are typical of an exogenous virus: it grows to high titers in tissue culture, and it is oncogenic in vivo. To accurately define the genetic region responsible for these properties, we determined the nucleotide sequences of the recombinant and its RAV-0 parent by using molecular clones of their DNA. These were compared with sequences already available for PrRSV-C, a virus closely related to the exogenous parent td-PrRSV-B. The results suggested that the crossover event which generated NTRE 7 took place in a region -501 to -401 nucleotides from the 3' end of the td-PrRSV parental genome and that sequences to the right of the recombination region were responsible for its growth properties and oncogenic potential. These sequences included a 148-base-pair exogenous-virus-specific region that was absent from the RAV-0 genome and the U3 region of the long terminal repeat. Since the exogenous-virus-specific sequences are expected to be missing from transformation-defective mutants of the Schmidt-Ruppin strain of RSV, which, like other exogenous viruses, grow to high titers in tissue culture and are oncogenic in vivo, we concluded that the growth properties and oncogenic potential of the exogenous viruses are determined by sequences in the U3 region of the long terminal repeat. However, we propose that the exogenous-virus-specific region may play a role in determining the oncogenic spectrum of a given oncogenic virus.
NTRE 7是一种禽逆转录病毒,它由内源性非致癌性罗氏相关病毒0(RAV-0)与致癌性外源性转化缺陷型(td)罗氏肉瘤病毒B布拉格株(td-PrRSV-B)重组而成。寡核苷酸图谱分析表明,除了3'端序列源自td-PrRSV-B外,重组病毒与其RAV-0亲本无法区分。然而,该病毒表现出外源性病毒的典型特性:它在组织培养中能达到高滴度,并且在体内具有致癌性。为了准确界定导致这些特性的基因区域,我们利用重组病毒及其RAV-0亲本的DNA分子克隆测定了它们的核苷酸序列。将这些序列与PrRSV-C的序列进行了比较,PrRSV-C是一种与外源性亲本td-PrRSV-B密切相关的病毒。结果表明,产生NTRE 7的交叉事件发生在td-PrRSV亲本基因组3'端-501至-401个核苷酸的区域,并且重组区域右侧的序列决定了其生长特性和致癌潜力。这些序列包括一个148个碱基对的外源性病毒特异性区域,该区域在RAV-0基因组中不存在,以及长末端重复序列的U3区域。由于预计施密特-鲁平株RSV的转化缺陷型突变体中会缺失外源性病毒特异性序列,而这些突变体与其他外源性病毒一样,在组织培养中能达到高滴度且在体内具有致癌性,因此我们得出结论,外源性病毒的生长特性和致癌潜力由长末端重复序列的U3区域中的序列决定。然而,我们提出外源性病毒特异性区域可能在决定特定致癌病毒的致癌谱方面发挥作用。