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第二组内含子RNA在体外催化RNA的重组。

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

作者信息

Mörl M, Schmelzer C

机构信息

Institut für Genetik und Mikrobiologie, Universität München, FRG.

出版信息

Nucleic Acids Res. 1990 Nov 25;18(22):6545-51. doi: 10.1093/nar/18.22.6545.

Abstract

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.

摘要

我们报道了由自我剪接的酵母线粒体II类内含子bl1介导的一种新型反应的首个证据;即RNA分子在体外的位点特异性重组。将内含子套索与两种不同的RNA一起温育,每种RNA都含有一段与内含子外显子结合位点1(EBS1)互补的短序列,会形成新的重组RNA。由于这种由内含子介导的基因片段重排,RNA1的5'部分与RNA2的3'部分连接,反之,RNA2的5'部分与RNA1的3'部分连接。重组接头的序列分析表明,重组位点精确位于内含子结合位点1(IBS1)的3'端。推测的重组机制涉及在反向剪接反应的第一步之后RNA 5'部分的交换。讨论了该机制在体内和生命起源前进化过程中的可能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b234/332608/4389f836be0a/nar00206-0080-a.jpg

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