Latt S A, Goff S P, Tabin C J, Paskind M, Wang J Y, Baltimore D
J Virol. 1983 Mar;45(3):1195-9. doi: 10.1128/JVI.45.3.1195-1199.1983.
Circular duplex reverse transcripts of the genome of a strain of Abelson murine leukemia virus that encodes a 160,000-molecular-weight protein were isolated, cleaved with HindIII restriction endonuclease, and cloned into the unique HindIII site of lambda phage Charon 21A. Recombinant phage clones, some of which were infectious in transfection assays, were found to contain a 789-base-pair region specific for Abelson murine leukemia virus; this region is not found in other strains of this virus. The extra sequence was localized by restriction endonuclease and electron microscopic heteroduplex analysis. Sequence analysis showed no homology at the ends of the extra sequence, implying that it was deleted by an event that did not utilize sequence homology. The sequence of this unique region has an open reading frame through its entirety.
分离出编码160,000分子量蛋白质的艾贝尔森鼠白血病病毒株基因组的环状双链逆转录物,用HindIII限制性内切酶切割,并克隆到λ噬菌体Charon 21A的唯一HindIII位点。发现一些重组噬菌体克隆在转染试验中具有感染性,它们含有一个对艾贝尔森鼠白血病病毒特异的789碱基对区域;该区域在该病毒的其他毒株中未发现。通过限制性内切酶和电子显微镜异源双链分析对额外序列进行了定位。序列分析表明,额外序列的末端没有同源性,这意味着它是通过一个不利用序列同源性的事件缺失的。这个独特区域的序列从头到尾都有一个开放阅读框。