Breaker R R, Joyce G F
Department of Chemistry, Scripps Research Institute, La Jolla, CA 92037.
Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):6093-7. doi: 10.1073/pnas.91.13.6093.
The technique of self-sustained sequence replication allows isothermal amplification of DNA and RNA molecules in vitro. This method relies on the activities of a reverse transcriptase and a DNA-dependent RNA polymerase to amplify specific nucleic acid sequences. We have modified this protocol to allow selective amplification of RNAs that catalyze a particular chemical reaction. During an in vitro RNA evolution experiment employing this modified system, a unique class of "selfish" RNAs emerged and replicated to the exclusion of the intended RNAs. Members of this class of selfish molecules, termed RNA Z, amplify efficiently despite their inability to catalyze the target chemical reaction. Their amplification requires the action of both reverse transcriptase and RNA polymerase and involves the synthesis of both DNA and RNA replication intermediates. The proposed amplification mechanism for RNA Z involves the formation of a DNA hairpin that functions as a template for transcription by RNA polymerase. This arrangement links the two strands of the DNA, resulting in the production of RNA transcripts that contain an embedded RNA polymerase promoter sequence.
自我维持序列复制技术可在体外对DNA和RNA分子进行等温扩增。该方法依赖逆转录酶和依赖DNA的RNA聚合酶的活性来扩增特定核酸序列。我们对该方案进行了改进,以实现对催化特定化学反应的RNA的选择性扩增。在使用这种改进系统进行的体外RNA进化实验中,一类独特的“自私”RNA出现并复制,从而排除了预期的RNA。这类自私分子被称为RNA Z,尽管它们无法催化目标化学反应,但仍能高效扩增。它们的扩增需要逆转录酶和RNA聚合酶的共同作用,并且涉及DNA和RNA复制中间体的合成。提出的RNA Z扩增机制涉及形成一个DNA发夹结构,该结构作为RNA聚合酶转录的模板。这种排列方式将DNA的两条链连接起来,从而产生包含嵌入RNA聚合酶启动子序列的RNA转录本。