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从头到尾:5'端和3'端位置的tRNA编辑

From end to end: tRNA editing at 5'- and 3'-terminal positions.

作者信息

Betat Heike, Long Yicheng, Jackman Jane E, Mörl Mario

机构信息

Institute for Biochemistry, University of Leipzig, Brüderstraße 34, 04103 Leipzig, Germany.

Department of Chemistry and Biochemistry, Center for RNA Biology and Ohio State Biochemistry Program, the Ohio State University, Columbus, OH 43210, USA.

出版信息

Int J Mol Sci. 2014 Dec 22;15(12):23975-98. doi: 10.3390/ijms151223975.

Abstract

During maturation, tRNA molecules undergo a series of individual processing steps, ranging from exo- and endonucleolytic trimming reactions at their 5'- and 3'-ends, specific base modifications and intron removal to the addition of the conserved 3'-terminal CCA sequence. Especially in mitochondria, this plethora of processing steps is completed by various editing events, where base identities at internal positions are changed and/or nucleotides at 5'- and 3'-ends are replaced or incorporated. In this review, we will focus predominantly on the latter reactions, where a growing number of cases indicate that these editing events represent a rather frequent and widespread phenomenon. While the mechanistic basis for 5'- and 3'-end editing differs dramatically, both reactions represent an absolute requirement for generating a functional tRNA. Current in vivo and in vitro model systems support a scenario in which these highly specific maturation reactions might have evolved out of ancient promiscuous RNA polymerization or quality control systems.

摘要

在成熟过程中,tRNA分子会经历一系列单独的加工步骤,从其5'端和3'端的外切核酸酶和内切核酸酶修剪反应、特定碱基修饰、内含子去除到保守的3'末端CCA序列的添加。特别是在线粒体中,这大量的加工步骤是通过各种编辑事件完成的,其中内部位置的碱基身份会发生变化,和/或5'端和3'端的核苷酸会被替换或掺入。在本综述中,我们将主要关注后一种反应,越来越多的案例表明这些编辑事件是一种相当频繁且广泛的现象。虽然5'端和3'端编辑的机制基础有很大差异,但这两种反应都是生成功能性tRNA的绝对必要条件。目前的体内和体外模型系统支持这样一种情况,即这些高度特异性的成熟反应可能是从古老的混杂RNA聚合或质量控制系统演变而来的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/210b/4284800/515bf743d4c5/ijms-15-23975-g001.jpg

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