Large-scale analysis of structural, sequence and thermodynamic characteristics of A-to-I RNA editing sites in human Alu repeats

被引:33
作者
Kleinberger, Yoav [1 ]
Eisenberg, Eli [1 ]
机构
[1] Tel Aviv Univ, Raymond & Beverly Sackler Sch Phys & Astron, IL-69978 Tel Aviv, Israel
来源
BMC GENOMICS | 2010年 / 11卷
基金
以色列科学基金会;
关键词
DOUBLE-STRANDED-RNA; PRE-MESSENGER-RNA; SEROTONIN 2C RECEPTOR; ADENOSINE-DEAMINASE; HUMAN TRANSCRIPTOME; CAENORHABDITIS-ELEGANS; ADAR1; CLEAVAGE; GENE; ENZYME;
D O I
10.1186/1471-2164-11-453
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Alu repeats in the human transcriptome undergo massive adenosine to inosine RNA editing. This process is selective, as editing efficiency varies greatly among different adenosines. Several studies have identified weak sequence motifs characterizing the editing sites, but these alone do not account for the large diversity observed. Results: Here we build a dataset of 29,971 editing sites and use it to characterize editing preferences. We focus on structural aspects, studying the double-stranded RNA structure of the Alu repeats, and show the editing frequency of a given site to depend strongly on the micro-structure it resides in. Surprisingly, we find that interior loops, and especially the nucleotides at their edges, are more likely to be edited than helices. In addition, the sequence motifs characterizing editing sites vary with the micro-structure. Finally, we show that thermodynamic stability of the site is important for its editing. Conclusions: Analysis of a large dataset of editing events reveals more information on sequence and structural motifs characterizing the A-to-I editing process
引用
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页数:17
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