Haegeman G, Fiers W
J Virol. 1978 Mar;25(3):824-30. doi: 10.1128/JVI.25.3.824-830.1978.
32P-labeled, late simian virus 40-specific RNA was isoalted from infected CV1 cells and completely degraded with RNase T2 and bacterial alkaline phosphatase. The RNase-resistant material was fractionated two dimensionally and further characterized with Penicillium nuclease and nucleotide pyrophosphatase. Two major 5' termini were identified in late simian virus 40 RNA, namely, 7-methyl Gppp 2',6-dimethyl ApUp and 7-methyl Gppp 2',6-dimethyl Ap 2'-methyl, UpUp. Both 5' termini are present in unfractionated viral RNA as well as in the separated 16S and 19S species. As both caps differ only in secondary modification, it is possible that they are derived from the same site on the DNA. The relatively higher cap II content of the 16S mRNA may be related to its slower rate of turnover.
从感染的CV1细胞中分离出32P标记的、晚期猿猴病毒40特异性RNA,并用核糖核酸酶T2和细菌碱性磷酸酶将其完全降解。对核糖核酸酶抗性物质进行二维分级分离,并用青霉核酸酶和核苷酸焦磷酸酶进一步鉴定。在晚期猿猴病毒40 RNA中鉴定出两个主要的5'末端,即7-甲基Gppp 2',6-二甲基ApUp和7-甲基Gppp 2',6-二甲基Ap 2'-甲基,UpUp。这两个5'末端既存在于未分级的病毒RNA中,也存在于分离的16S和19S物种中。由于两种帽结构仅在二级修饰上有所不同,因此它们有可能来自DNA上的同一位点。16S mRNA相对较高的帽II含量可能与其较慢的周转速率有关。