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Group II intron RNA-catalyzed recombination of RNA in vitro.

机译:II组内含子RNA催化的RNA体外重组。

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摘要

We report the first evidence for a novel reaction mediated by the self-splicing yeast mitochondrial group II intron bl1; the site-specific recombination of RNA molecules in vitro. Upon incubation of the intron lariat with two different RNAs, each harbouring a short sequence complementary to exon binding site 1 (EBS1) of the intron, novel recombined RNAs are formed. As a result of this intron-mediated shuffling of gene segments, the 5' part of RNA1 is ligated to the 3' part of RNA2 and, reciprocally, the 5' part of RNA2 to the 3' part of RNA1. Sequence analysis of the recombinant junction shows that the site of recombination is precisely located 3' to intron binding site 1 (IBS1). The hypothesized mechanism of recombination involves exchange of RNA 5' parts after the first step of a reverse splicing reaction. The possible role of this mechanism in vivo and during prebiotic evolution is discussed.
机译:我们报告了由自我剪接的酵母线粒体II组内含子bl1介导的新型反应的第一个证据; RNA分子在体外的位点特异性重组。用两个不同的RNA孵育内含子套索蛋白后,每个RNA都包含一个与内含子的外显子结合位点1(EBS1)互补的短序列,形成了新的重组RNA。由于内含子介导的基因片段改组,RNA1的5'部分与RNA2的3'部分相连,而RNA2的5'部分与RNA1的3'部分相连。重组接头的序列分析表明重组位点恰好位于内含子结合位点1(IBS1)的3'端。假设的重组机制涉及在反向剪接反应的第一步之后交换RNA 5'部分。讨论了该机制在体内和益生元进化过程中的可能作用。

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