Keene J D, Schubert M, Lazzarini R A, Rosenberg M
Proc Natl Acad Sci U S A. 1978 Jul;75(7):3225-9. doi: 10.1073/pnas.75.7.3225.
Vesicular stomatitis virus (VSV) and defective interfering (DI) particle RNAs were labeled at their 3' ends by using RNA ligase and cytidine 3',5'-bis[32P]phosphate. The RNAs were subjected to partial digestion with alkali and analyzed by oligonucleotide fingerprinting in two dimensions. VSV and DI particle RNAs have complete sequence homology for the first eight bases from the 3' end. The following four positions contain three mismatched nucleotides in which guanosine residues in one strand are replaced by uridine residues in the other. There is again complete homology for the next five bases (positions 13-17). The locations of purine residues within the sequence were confirmed by partial digestion with RNase T1 and RNase U2 and separation by size on 20% acrylamide gels. The latter method also indicated that sequences of VSV and DI particle RNAs diverge beyond the 18th nucleotide from the 3' termini.
水泡性口炎病毒(VSV)和缺陷干扰(DI)颗粒RNA在其3'末端通过使用RNA连接酶和胞苷3',5'-双[32P]磷酸进行标记。RNA用碱进行部分消化,并通过二维寡核苷酸指纹图谱进行分析。VSV和DI颗粒RNA从3'末端起的前八个碱基具有完全的序列同源性。接下来的四个位置包含三个错配的核苷酸,其中一条链中的鸟苷残基被另一条链中的尿苷残基取代。接下来的五个碱基(第13 - 17位)再次具有完全同源性。通过用核糖核酸酶T1和核糖核酸酶U2进行部分消化并在20%丙烯酰胺凝胶上按大小分离,确定了序列中嘌呤残基的位置。后一种方法还表明,VSV和DI颗粒RNA的序列在从3'末端起第18个核苷酸之后发生分歧。