Steffen D, Bird S, Rowe W P, Weinberg R A
Proc Natl Acad Sci U S A. 1979 Sep;76(9):4554-8. doi: 10.1073/pnas.76.9.4554.
The proviruses of the N-tropic, ecotropic virus (AKV) of AKR mice (Akv-1, Akv-2) have been studied by the Southern gel--filter transfer technique. These proviruses can be detected by cleavage of cell DNA by BamHI endonuclease, which yields characteristic subgenomic DNA fragments upon cleavage of this type of provirus. Proviruses integrated into different sites in the mouse genome can be resolved with EcoRI endonuclease, which does not cleave the AKV proviruses. Use of congenic and backcrossed mice and a radioactive DNA probe enriched for AKV sequences has allowed identification of the EcoRI fragments carrying the proviruses of the genetically defined Akv-1 and Akv-2 loci. Novel proviruses introduced by superinfection of cultured AKR cells with AKV and present in leukemic cells from AKR mice have also been identified. Comparison of substrains of AKR mice indicates some heterogeneity in their spectra of proviruses.
利用Southern凝胶-滤膜转移技术对AKR小鼠的N-嗜性、亲嗜性病毒(AKV)(Akv-1、Akv-2)的前病毒进行了研究。通过用BamHI核酸内切酶切割细胞DNA可检测到这些前病毒,该酶在切割此类前病毒时会产生特征性的亚基因组DNA片段。整合到小鼠基因组不同位点的前病毒可用EcoRI核酸内切酶进行分辨,该酶不会切割AKV前病毒。使用同源近交系和回交小鼠以及富含AKV序列的放射性DNA探针,已能够鉴定携带遗传定义的Akv-1和Akv-2位点前病毒的EcoRI片段。还鉴定了通过用AKV对培养的AKR细胞进行超感染而引入并存在于AKR小鼠白血病细胞中的新型前病毒。对AKR小鼠亚系的比较表明,它们前病毒谱存在一些异质性。