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通过比较基因组学鉴定编码tRNA修饰酶的基因。

Identification of genes encoding tRNA modification enzymes by comparative genomics.

作者信息

de Crécy-Lagard Valérie

机构信息

Department of Microbiology and Cell Science, University of Florida, Gainesville, FL, USA.

出版信息

Methods Enzymol. 2007;425:153-83. doi: 10.1016/S0076-6879(07)25007-4.

DOI:10.1016/S0076-6879(07)25007-4
PMID:17673083
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3034448/
Abstract

As the molecular adapters between codons and amino acids, transfer-RNAs are pivotal molecules of the genetic code. The coding properties of a tRNA molecule do not reside only in its primary sequence. Posttranscriptional nucleoside modifications, particularly in the anticodon loop, can modify cognate codon recognition, affect aminoacylation properties, or stabilize the codon-anticodon wobble base pairing to prevent ribosomal frameshifting. Despite a wealth of biophysical and structural knowledge of the tRNA modifications themselves, their pathways of biosynthesis had been until recently only partially characterized. This discrepancy was mainly due to the lack of obvious phenotypes for tRNA modification-deficient strains and to the difficulty of the biochemical assays used to detect tRNA modifications. However, the availability of hundreds of whole-genome sequences has allowed the identification of many of these missing tRNA-modification genes. This chapter reviews the methods that were used to identify these genes with a special emphasis on the comparative genomic approaches. Methods that link gene and function but do not rely on sequence homology will be detailed, with examples taken from the tRNA modification field.

摘要

作为密码子与氨基酸之间的分子衔接器,转运RNA是遗传密码的关键分子。tRNA分子的编码特性并非仅取决于其一级序列。转录后核苷修饰,尤其是反密码子环中的修饰,可改变对同源密码子的识别、影响氨酰化特性,或稳定密码子-反密码子摆动碱基对以防止核糖体移码。尽管对tRNA修饰本身已有丰富的生物物理和结构知识,但直到最近其生物合成途径仍仅得到部分表征。这种差异主要是由于缺乏tRNA修饰缺陷菌株的明显表型,以及用于检测tRNA修饰的生化分析存在困难。然而,数百个全基因组序列的可得性使得许多这些缺失tRNA修饰基因得以鉴定。本章回顾了用于鉴定这些基因的方法,特别强调了比较基因组学方法。将详细介绍那些不依赖序列同源性而将基因与功能联系起来的方法,并从tRNA修饰领域举例说明。

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