A-to-I editing of protein coding and noncoding RNAs

被引:46
作者
Mallela, Arka [1 ]
Nishikura, Kazuko [1 ]
机构
[1] Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
RNA; RNA editing; ADAR; inosine; miRNA; siRNA; adenosine deaminase; dsRNA; DOUBLE-STRANDED-RNA; DSRNA-ADENOSINE-DEAMINASE; DNA BINDING DOMAIN; UNWINDING ACTIVITY; GABA(A) RECEPTOR; MAMMALIAN-CELLS; ADAR DEAMINASES; MESSENGER-RNA; ENZYME ADAR1; HUMAN GENOME;
D O I
10.3109/10409238.2012.714350
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adenosine deaminase acting on RNA (ADAR) catalyzes the hydrolytic deamination of adenosine to inosine in double-stranded RNA (dsRNA) substrates. Inosine pairs preferentially with cytidine, as opposed to uridine; therefore, ADAR editing alters the sequence and base pairing properties of both protein-coding and non-coding RNA. Editing can directly alter the sequence of protein-coding transcripts and modify splicing, or affect a variety of non-coding targets, including microRNA, small interfering RNA, viral transcripts, and repeat elements such as Alu and LINE. Such editing has a wide range of physiological effects, including modification of targets in the brain and in disease states.
引用
收藏
页码:493 / 501
页数:9
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