Bina-Stein M, Thoren M, Salzman N, Thomspon J A
Proc Natl Acad Sci U S A. 1979 Feb;76(2):731-5. doi: 10.1073/pnas.76.2.731.
A method for the determination of the primary structure of spliced mRNA junction and leader sequences is described. By analogy to the DNA sequencing procedure of Sanger et al. [Sanger, F., Nicklen, S. & Coulson, A. R. (1977) Proc. Natl. Acad. Sci USA 74, 5463--5467], we use 2",3'-dideoxynucleoside triphosphates as chain-terminating inhibitors of the reverse transcriptase (RNA-dependent DNA polymerase) reaction. By using specific DNA restriction fragments as primers in combination with this technique, we have determined the sequence of the spliced junction between the body and the leader sequence of the 16S late mRNA of simian virus 40. The method described should be of general utility in mapping spliced mRNA regions for which the corresponding protein sequence (if any) is unknown.
本文描述了一种测定剪接mRNA接头和前导序列一级结构的方法。类比于桑格等人的DNA测序程序[桑格,F.,尼克伦,S. & 库尔森,A. R.(1977年)《美国国家科学院院刊》74,5463 - 5467],我们使用2',3'-双脱氧核苷三磷酸作为逆转录酶(RNA依赖性DNA聚合酶)反应的链终止抑制剂。通过将特定的DNA限制性片段用作引物并结合该技术,我们确定了猴病毒40的16S晚期mRNA主体与前导序列之间剪接接头的序列。所描述的方法在绘制相应蛋白质序列(如果有的话)未知的剪接mRNA区域时应具有普遍实用性。