ADAR editing in double-stranded UTRs and other noncoding RNA sequences

被引:121
作者
Hundley, Heather A. [1 ,2 ]
Bass, Brenda L. [1 ]
机构
[1] Univ Utah, Dept Biochem, Salt Lake City, UT 84112 USA
[2] Indiana Univ, Bloomington, IN 47405 USA
基金
美国国家卫生研究院;
关键词
GENE-EXPRESSION; ADENOSINE DEAMINASES; UNWINDING ACTIVITY; MESSENGER-RNAS; PROTEIN P100; INOSINE; DSRNA; COACTIVATOR; RETENTION; COMPLEX;
D O I
10.1016/j.tibs.2010.02.008
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
ADARs are a family of enzymes, present in all animals, that convert adenosine to inosine within double-stranded RNA (dsRNA). Inosine and adenosine have different base-pairing properties, and thus, editing alters RNA structure, coding potential and splicing patterns. The first ADAR substrates identified were edited in codons, and ADARs were presumed to function primarily in proteome diversification. Although this is an important function of ADARs, especially in the nervous system, editing in coding sequences is rare compared to editing in noncoding sequences. Introns and untranslated regions of mRNA are the primary noncoding targets, but editing also occurs in small RNAs, such as miRNAs. Although the role of editing in noncoding sequences remains unclear, ongoing research suggests functions in the regulation of a variety of post-transcriptional processes.
引用
收藏
页码:377 / 383
页数:7
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