Duesberg P H, Wang L H, Beemon K, Kawai S, Hanafusa H
Hamatol Bluttransfus. 1976;19:327-40. doi: 10.1007/978-3-642-87524-3_34.
A procedure has been developed to map the genetic elements of avian tumor virus RNA, which has a molecular weight of about 3 X 10(6) daltons and a poly(A) sequence at the 3' end. For this purpose, about 30 RNase T1-resistant oligonucleotides were ordered relative to the 3'-poly(A) terminus of the RNA, to construct an oligonucleotide map of viral RNAs. A cluster of seven envelope gene (env)-specific oligonucleotides, identified by their absence from the otherwise very similar oligonucleotide map of an envelope-defective deletion mutant (which lacks the major viral glycoprotein), mapped at a distance of 0.9 to 1.6 X 10(6) daltons from the poly(A) end of sarcoma virus RNA. A cluster of three sarcoma gene (src)-specific oligonucleotides, identified by their absence from the otherwise nearly identical oligonucleotide map of a transformation-defective deletion mutant mapped at a distance of 0.2 to 0.6 X 10(6) daltons from the poly(A) end of sarcoma virus RNA. The oligonucleotide maps of sarcoma viruses and of related deletion mutants were the same from the poly(A) end up to 0.2 X 10(6) daltons and included one terminal oligonucleotide, termed C, which is found in all avian tumor viruses tested so far. Preliminary mapping experiments ordering the src-specific and env-specific oligonucleotides of recombinants, selected for sarcoma and envelope genes of different parents, agree with those obtained by comparing maps of wild type viruses and deletion mutants. A partial genetic map consistent with these results suggests that the src gene maps between the env gene and the 3'-poly(A) end of viral RNA. This map reads: poly(A)-src-env-(pol, gag).
已开发出一种程序来绘制禽肿瘤病毒RNA的遗传元件图谱,该RNA的分子量约为3×10⁶道尔顿,3'端有一个聚腺苷酸(poly(A))序列。为此,相对于RNA的3'-聚腺苷酸末端,排列了约30个对核糖核酸酶T1有抗性的寡核苷酸,以构建病毒RNA的寡核苷酸图谱。一组七个包膜基因(env)特异性寡核苷酸,通过它们在包膜缺陷型缺失突变体(缺乏主要病毒糖蛋白)的其他非常相似的寡核苷酸图谱中不存在而得以鉴定,它们位于肉瘤病毒RNA的聚腺苷酸末端0.9至1.6×10⁶道尔顿的距离处。一组三个肉瘤基因(src)特异性寡核苷酸,通过它们在转化缺陷型缺失突变体的其他几乎相同的寡核苷酸图谱中不存在而得以鉴定,该突变体位于肉瘤病毒RNA的聚腺苷酸末端0.2至0.6×10⁶道尔顿的距离处。肉瘤病毒及其相关缺失突变体的寡核苷酸图谱从聚腺苷酸末端到0.2×10⁶道尔顿是相同的,并且包括一个末端寡核苷酸,称为C,在迄今为止测试的所有禽肿瘤病毒中都能找到。对不同亲本的肉瘤和包膜基因选择的重组体的src特异性和env特异性寡核苷酸进行排序的初步图谱实验,与通过比较野生型病毒和缺失突变体的图谱获得的结果一致。与这些结果一致的部分遗传图谱表明,src基因位于env基因和病毒RNA的3'-聚腺苷酸末端之间。该图谱如下:聚腺苷酸-src-env-(pol,gag)。