Zhang Y, Liu W Y, Feng Y X, Wang T P
Department of Bioscience and Technology, Shanghai Jiao-Tong University, China.
Anal Biochem. 1987 Jun;163(2):513-6. doi: 10.1016/0003-2697(87)90256-9.
A simple and rapid solid-phase RNA sequencing method has been developed based on Peattie's direct chemical method. 3'-Terminally labeled RNA was immobilized on DEAE-cellulose sheets and followed by specific modification with dimethyl sulfate, diethylpyrocarbonate, hydroxylamine (at pH 10 for the uridine and pH 5.5 for the cytidine reaction), and cleavage reaction with aniline. RNA fragments were washed from the DEAE-cellulose sheets using salt solutions, precipitated with ethanol, and separated by 15% polyacrylamide gel electrophoresis. Due to the complete removal of the impurities normally present in the solution method, the higher resolution of the sequencing bands and lower background on the autoradiograph make this solid-phase technique more efficient. This solid-phase technique is much faster and more convenient than the original method.
基于皮蒂的直接化学法,已开发出一种简单快速的固相RNA测序方法。3'末端标记的RNA固定在二乙氨基乙基纤维素片上,随后用硫酸二甲酯、焦碳酸二乙酯、羟胺(尿苷反应pH值为10,胞苷反应pH值为5.5)进行特异性修饰,并用苯胺进行裂解反应。用盐溶液从二乙氨基乙基纤维素片上洗下RNA片段,用乙醇沉淀,并用15%聚丙烯酰胺凝胶电泳分离。由于完全去除了溶液法中通常存在的杂质,测序条带的分辨率更高,放射自显影片上的背景更低,使得这种固相技术更高效。这种固相技术比原始方法更快、更方便。