Rosenthal A, Schulz J, Gross B
Nucleic Acids Symp Ser. 1985(16):189-92.
A solid-phase method for simultaneous sequencing of different long RNA fragments has been developed using Whatman DE 81 anion-exchange paper as the support. The approach involves 8 operations including: immobilization of heat-denatured 3'-end labeled RNA fragment on DE 81 paper; washing; modification reactions; washing; aniline reaction; washing; RNA desorption by salt and ethanol precipitation. For modifying the RNA, the following reactions were selected for the routine: G with dimethylsulfate at 90 degrees C/sodium borohydride at 0 degrees C, A + G with diethylpyrocarbonate at 90 degrees C, U + C with hydrazine at 0 degrees C and C with hydrazine/5M NaCl at 0 degrees C. The losses of RNA material during the reactions with large excess of reactants were 50% during the reduction with NaBH4 and 30% during C-reaction. Almost no losses were observed during aniline reaction. The RNA could be recovered by desorption with 2M NaClO4 in 50-70% yield. The whole solid-phase procedure up to the sequencing gel takes about 2 hours and is much faster and more convenient than chemical RNA sequencing in solution according to Peattie, especially if many fragments are to be processed.
一种使用沃特曼DE 81阴离子交换纸作为载体同时对不同长RNA片段进行测序的固相方法已被开发出来。该方法包括8个操作步骤,即:将热变性的3'-末端标记RNA片段固定在DE 81纸上;洗涤;修饰反应;洗涤;苯胺反应;洗涤;通过盐析和乙醇沉淀进行RNA解吸。为了修饰RNA,选择了以下常规反应:用硫酸二甲酯在90℃/硼氢化钠在0℃修饰G,用焦碳酸二乙酯在90℃修饰A + G,用肼在0℃修饰U + C,用肼/5M氯化钠在0℃修饰C。在用大量过量反应物进行反应时,RNA材料在硼氢化钠还原过程中的损失为50%,在C反应过程中的损失为30%。在苯胺反应过程中几乎没有观察到损失。RNA可以用2M高氯酸钠解吸回收,回收率为50-70%。在测序凝胶之前的整个固相过程大约需要2小时,并且比根据佩蒂的溶液化学RNA测序更快、更方便,特别是如果要处理许多片段的话。