Tsai C H, Dreher T W
Department of Agricultural Chemistry, Oregon State University, Corvallis 97331-6502.
Biotechniques. 1993 Jan;14(1):58-61.
We demonstrate the feasibility of using PCR to economically amplify sufficient template to permit the transcription by T7 RNA polymerase of preparative amounts of RNAs for biochemical analyses. We show that a standard 100-microliter PCR amplification of a fragment from the 3' end of the genomic cDNA of turnip yellow mosaic virus yields enough template to support the synthesis of about 50 micrograms of a 264-nucleotide-long transcript. The choice of the 3' primer defines the 3' terminus of the transcripts, although, as with transcription from DNA linearized by restriction digestion, a subpopulation of transcripts with one or two additional 3' nucleotides is present. This PCR-based approach can be adapted to the rapid generation of RNAs with different 3' termini and with mutations near the 3' end.
我们证明了使用聚合酶链式反应(PCR)经济地扩增足够模板的可行性,以允许通过T7 RNA聚合酶转录制备用于生化分析的RNA量。我们表明,对芜菁黄花叶病毒基因组cDNA 3'端的一个片段进行标准的100微升PCR扩增,可产生足够的模板,以支持合成约50微克长度为264个核苷酸的转录本。3'引物的选择决定了转录本的3'末端,不过,与通过限制性消化线性化的DNA转录一样,存在一个具有一个或两个额外3'核苷酸的转录本子群体。这种基于PCR的方法可适用于快速生成具有不同3'末端且3'端附近有突变的RNA。