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RNA 世界中双重角色的悖论:解决稳定折叠和模板能力之间的冲突。

The paradox of dual roles in the RNA world: resolving the conflict between stable folding and templating ability.

出版信息

J Mol Evol. 2013 Sep;77(3):55-63. doi: 10.1007/s00239-013-9584-x.

DOI:10.1007/s00239-013-9584-x
PMID:24078151
Abstract

The hypothesized dual roles of RNA as both information carrier and biocatalyst during the earliest stages of life require a combination of features: good templating ability (for replication) and stable folding (for ribozymes). However, this poses the following paradox: well-folded sequences are poor templates for copying, but poorly folded sequences are unlikely to be good ribozymes. Here, we describe a strategy to overcome this dilemma through G:U wobble pairing in RNA. Unlike Watson-Crick base pairs, wobble pairs contribute highly to the energetic stability of the folded structure of their sequence, but only slightly, if at all, to the stability of the folded reverse complement. Sequences in the RNA World might thereby combine stable folding of the ribozyme with an unstructured, reverse-complementary genome, resulting in a "division of labor" between the strands. We demonstrate this strategy using computational simulations of RNA folding and an experimental model of early replication, nonenzymatic template-directed RNA primer extension. Additional study is needed to solve other problems associated with a complete replication cycle, including separation of strands after copying. Interestingly, viroid RNA sequences, which have been suggested to be relics of an RNA World (Diener, Proc Natl Acad Sci USA 86:9370-9374, 1989), also show significant asymmetry in folding energy between the infectious (+) and template (-) strands due to G:U pairing, suggesting that this strategy may even be used by replicators in the present day.

摘要

在生命起源的早期,RNA 作为信息载体和生物催化剂的双重作用假设需要结合以下特征:良好的模板能力(用于复制)和稳定的折叠(用于核酶)。然而,这带来了以下悖论:折叠良好的序列不利于复制,而折叠不良的序列不太可能成为好的核酶。在这里,我们描述了一种通过 RNA 中的 G:U 摆动配对来克服这一困境的策略。与 Watson-Crick 碱基对不同,摆动配对高度有助于其序列折叠结构的能量稳定性,但对折叠反向互补物的稳定性几乎没有影响。因此,RNA 世界中的序列可能将核酶的稳定折叠与无结构的反向互补基因组结合起来,从而导致链之间的“分工”。我们使用 RNA 折叠的计算模拟和非酶模板指导的 RNA 引物延伸的实验模型来证明这一策略。需要进一步的研究来解决与完整复制周期相关的其他问题,包括复制后链的分离。有趣的是,类病毒 RNA 序列被认为是 RNA 世界的遗迹(Diener,Proc Natl Acad Sci USA 86:9370-9374, 1989),由于 G:U 配对,在折叠能之间也表现出显著的不对称性,这表明这种策略甚至可能被当今的复制子使用。

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