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RNA连接与tRNA的起源

RNA ligation and the origin of tRNA.

作者信息

Nagaswamy Uma, Fox George E

机构信息

Department of Biology and Biochemistry, 369 Science and Research Bldg. 2, University of Houston, Houston, TX 77204-5001, USA.

出版信息

Orig Life Evol Biosph. 2003 Apr;33(2):199-209. doi: 10.1023/a:1024658727570.

Abstract

A straightforward origin of transfer RNA, (tRNA), is difficult to envision because of the apparently complex idiosyncratic interaction between the D-loop and T-loop. Recently, multiple examples of the T-loop structural motif have been identified in ribosomal RNA. These examples show that the long-range interactions between the T-loop and D-loops seen in tRNA are not an essential part of the motif but rather are facilitated by it. Thus, the core T-loop structure could already have existed in a small RNA prior to the emergence of the tRNA. The tRNA might then have arisen by expansion of an RNA that carried the motif. With this idea in mind, Di Giulio's earlier hypothesis that tRNA evolved by a simple duplication or ligation of a minihelix RNA was re-examined. It is shown that an essentially modern tRNA structure can in fact be generated by the ligation of two 38-nucleotide RNA minihelices of appropriate sequence. Although rare, such sequences occur with sufficient frequency, (1 in 3 x 10(7)), that they could be found in a standard in vitro RNA selection experiment. The results demonstrate that a series of RNA duplications, as previously proposed, can in principal account for the origin of tRNA. More generally, the results point out that RNA ligation can be a powerful driving force for increased complexity in the RNA World.

摘要

由于D环和T环之间存在明显复杂的特异相互作用,因此很难设想转运RNA(tRNA)的直接起源。最近,在核糖体RNA中发现了多个T环结构基序的例子。这些例子表明,tRNA中所见的T环和D环之间的长程相互作用并非该基序的必要组成部分,而是由它促成的。因此,在tRNA出现之前,核心T环结构可能已经存在于一种小RNA中。然后,tRNA可能是由携带该基序的RNA扩展而来的。基于这一想法,重新审视了迪朱利奥早期提出的tRNA通过小螺旋RNA的简单复制或连接而进化的假说。结果表明,实际上可以通过连接两个具有适当序列的38个核苷酸的RNA小螺旋来生成一个基本现代的tRNA结构。尽管这种序列很罕见,但出现的频率足以使其在标准的体外RNA筛选实验中被发现(每3×10⁷个中有1个)。结果表明,如先前提出的那样,一系列RNA复制原则上可以解释tRNA的起源。更普遍地说,结果指出RNA连接可能是RNA世界中增加复杂性的强大驱动力。

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