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从两个遗传传递的莫洛尼白血病前病毒基因组获得的分子克隆的感染性和结构。

Infectivity and structure of molecular clones obtained from two genetically transmitted Moloney leukemia proviral genomes.

作者信息

Harbers K, Schnieke A, Stuhlmann H, Jaenisch R

出版信息

Nucleic Acids Res. 1982 Apr 24;10(8):2521-37. doi: 10.1093/nar/10.8.2521.

Abstract

The Mov-2 and Mov-10 substrains of mice, each carrying Moloney leukemia virus (= M-MuLV) in their germ line at the Mov-2 and Mov-10 locus, respectively, do occasionally at a later age (Mov-2) or not at all (Mov-10) activate infectious virus. The M-MuLV proviruses with flanking mouse sequences corresponding to the Mov-2 and Mov-10 locus, respectively, were molecularly cloned. Restriction enzyme analysis revealed no major deletions or insertions in the proviral genomes of the Mov-2 and Mov-10 locus. Both cloned DNAs induced XC plaques in a transfection assay. The specific infectivity, however, was very low and 3T3 cells transfected with the Mov-2 or Mov-10 clone did not produce infectious virus. Removing part of the 5' cellular sequences from the Mov-10 clone did not increase the infectivity. The results suggest that the M-MuLV integrated at the Mov-2 and Mov-10 locus carry a mutation which prevents synthesis of infectious virus but permits XC plaque induction by partial genome expression or synthesis of non-infectious particles.

摘要

Mov-2和Mov-10品系的小鼠,分别在其生殖系的Mov-2和Mov-10位点携带莫洛尼白血病病毒(=M-MuLV),Mov-2品系的小鼠在较晚年龄偶尔会激活感染性病毒,而Mov-10品系的小鼠则根本不会激活。分别与Mov-2和Mov-10位点对应的带有侧翼小鼠序列的M-MuLV前病毒被进行了分子克隆。限制性酶切分析显示,Mov-2和Mov-10位点的前病毒基因组中没有重大缺失或插入。在转染试验中,两种克隆的DNA都能诱导产生XC噬斑。然而,其特异性感染性非常低,用Mov-2或Mov-10克隆转染的3T3细胞不会产生感染性病毒。从Mov-10克隆中去除部分5'细胞序列并不会增加其感染性。结果表明,整合在Mov-2和Mov-10位点的M-MuLV携带一种突变,该突变阻止感染性病毒的合成,但允许通过部分基因组表达或非感染性颗粒的合成诱导XC噬斑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b72/320631/567385535a30/nar00377-0047-a.jpg

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