首页> 美国卫生研究院文献>Journal of Virology >Generation of AKR mink cell focus-forming viruses: a conserved single-copy xenotrope-like provirus provides recombinant long terminal repeat sequences.
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Generation of AKR mink cell focus-forming viruses: a conserved single-copy xenotrope-like provirus provides recombinant long terminal repeat sequences.

机译:AKR水貂细胞聚焦形成病毒的产生:保守的单拷贝异种菌状原病毒提供了重组的长末端重复序列。

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摘要

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.
机译:制备了来自包膜和长末端重复序列(LTR)区域的AKV和AKR貂细胞聚焦形成病毒特异性探针,用于研究AKR小鼠肿瘤组织中重组原病毒的结构。结果表明:(i)除重组gp70基因外,所有体细胞获得的原病毒都具有改变的U3 LTR; (ii)在体细胞获得的形成AKR貂细胞聚焦原病毒的很大一部分中,LTR包含衍生自相同异种样原病毒的序列; (iii)在几个小鼠品系中,每个基因组当量仅存在一次捐赠U3 LTR的亲本原病毒(Xeno-dL); (iv)在含有Xeno-dL原病毒的菌株中,原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,形成貂细胞聚焦点的gp70序列与Xeno-dL不同,来源于亲本原病毒。因此,至少有两个非亲性亲本参与生成致白血病的AKR貂细胞聚焦形成病毒的生成:类异种病毒,Xeno-dL,捐赠的U3 LTR序列和另一种类异种病毒或提供gp70序列的病毒。

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