Perbal B, Cline J M, Hillyard R L, Baluda M A
J Virol. 1983 Mar;45(3):925-40. doi: 10.1128/JVI.45.3.925-940.1983.
Several lambda proto-amv recombinants isolated from a lambda Charon 4A library of leukemic chicken DNA were analyzed by using various restriction endonucleases and hybridization with specific probes representing different regions of the transforming gene of avian myeloblastosis virus. The position of 30 sites for 11 different restriction endonucleases was established in the proto-amv region of chicken DNA. Identical restriction endonuclease maps were obtained for the normal and leukemic DNAs in the proto-amv domain, which covers 8 to 9 kilobases of DNA. The cellular genetic elements homologous to the cellular sequence (amv) inserted into the avian myeloblastosis virus genome are contained within six major proto-amv segments which are interrupted by at least five large DNA regions lacking homology with amv.
从白血病鸡DNA的λ噬菌体Charon 4A文库中分离出的几种λ原禽成髓细胞瘤病毒重组体,通过使用各种限制性内切酶以及与代表禽成髓细胞瘤病毒转化基因不同区域的特异性探针杂交进行分析。在鸡DNA的原禽成髓细胞瘤病毒区域确定了11种不同限制性内切酶的30个位点的位置。在覆盖8至9千碱基DNA的原禽成髓细胞瘤病毒结构域中,正常DNA和白血病DNA获得了相同的限制性内切酶图谱。与插入禽成髓细胞瘤病毒基因组的细胞序列(禽成髓细胞瘤病毒)同源的细胞遗传元件包含在六个主要的原禽成髓细胞瘤病毒片段中,这些片段被至少五个与禽成髓细胞瘤病毒缺乏同源性的大DNA区域中断。