Quint W, Boelens W, van Wezenbeek P, Cuypers T, Maandag E R, Selten G, Berns A
J Virol. 1984 May;50(2):432-8. doi: 10.1128/JVI.50.2.432-438.1984.
AKV and AKR mink cell focus-forming virus-specific probes from the envelope and long terminal repeat (LTR) regions were prepared for study of the structure of recombinant proviruses in tumor tissues of AKR mice. The results showed that (i) all somatically acquired proviruses possessed, besides a recombinant gp70 gene, an altered U3 LTR; (ii) in a substantial portion of the somatically acquired AKR mink cell focus-forming proviruses, the LTR comprised sequences derived from the same xenotropic-like provirus; (iii) this U3 LTR donating parental provirus (Xeno-dL) was present only once per genome equivalent in several mouse strains; (iv) in the strains containing the Xeno-dL provirus, the provirus was present in the same chromosomal site; (v) restriction analysis of the Xeno-dL revealed that the mink cell focus-forming gp70 sequences were derived from a parental provirus, different from Xeno-dL. Therefore, at least two non-ecotropic parents participate in the generation of leukemogenic AKR mink cell focus-forming viruses: a xenotropic-like virus, Xeno-dL, donating U3 LTR sequences, and another xenotropic-like virus or viruses providing gp70 sequences.
制备了来自包膜和长末端重复序列(LTR)区域的AKV和AKR水貂细胞集落形成病毒特异性探针,用于研究AKR小鼠肿瘤组织中重组前病毒的结构。结果表明:(i)除重组gp70基因外,所有体细胞获得的前病毒均具有改变的U3 LTR;(ii)在相当一部分体细胞获得的AKR水貂细胞集落形成前病毒中,LTR包含来自同一异种嗜性样前病毒的序列;(iii)这种捐赠U3 LTR的亲本前病毒(Xeno-dL)在几个小鼠品系中每个基因组当量仅出现一次;(iv)在含有Xeno-dL前病毒的品系中,该前病毒存在于相同的染色体位点;(v)对Xeno-dL的限制性分析表明,水貂细胞集落形成gp70序列来自与Xeno-dL不同的亲本前病毒。因此,至少有两个非嗜异性亲本参与致白血病的AKR水貂细胞集落形成病毒的产生:一种捐赠U3 LTR序列的异种嗜性样病毒Xeno-dL,以及另一种提供gp70序列的异种嗜性样病毒。