Fuke M, Busch H
Nucleic Acids Res. 1977 Feb;4(2):339-52. doi: 10.1093/nar/4.2.339.
The method employed to determine the sequence of a T1 RNase fragment, A-A-A-A-A-U-A-A-C-A-A-U-A-C-A-Gp, from Novikoff rat hepatoma 18S ribosomal RNA is described. This method is applicable to any oligoribonucleotide produced by specific endonucleases that leave the newly cleaved 5'-end free for labeling with polynucleotide kinase and gamma-(32p)-ATP. The (32p)-labeled oligoribonucleotide is subjected to partial endonucleolytic digestion and fractionated by two-dimensional homochromatography fingerprinting. The nucleotide sequence is determined by following mobility shifts of the labeled and partially digested oligoribonucleotides in homochromatography fingerprinting.
本文描述了用于确定来自诺维科夫大鼠肝癌18S核糖体RNA的T1核糖核酸酶片段A-A-A-A-A-U-A-A-C-A-A-U-A-C-A-Gp序列的方法。该方法适用于由特异性内切核酸酶产生的任何寡核糖核苷酸,这些酶使新切割的5'-末端游离,以便用多核苷酸激酶和γ-(32P)-ATP进行标记。将(32P)标记的寡核糖核苷酸进行部分内切核酸酶消化,并通过二维同系层析指纹图谱进行分级分离。通过跟踪标记的和部分消化的寡核糖核苷酸在同系层析指纹图谱中的迁移率变化来确定核苷酸序列。