RNA Editing by Mammalian ADARs

被引:88
作者
Hogg, Marion [1 ]
Paro, Simone [1 ]
Keegan, Liam P. [1 ]
O'Connell, Mary A. [1 ]
机构
[1] Western Gen Hosp, Human Genet Unit, Inst Genet & Mol Med, MRC, Edinburgh EH4 2XU, Midlothian, Scotland
来源
ADVANCES IN GENETICS, VOL 73 | 2011年 / 73卷
基金
英国医学研究理事会;
关键词
DOUBLE-STRANDED-RNA; DYSCHROMATOSIS SYMMETRICA HEREDITARIA; AMPA RECEPTOR SUBUNIT; PRE-MESSENGER-RNA; TRANSITION-STATE ANALOG; C-TERMINAL DOMAIN; ADENOSINE-DEAMINASE; BINDING DOMAINS; GLUR-B; HUMAN BRAIN;
D O I
10.1016/B978-0-12-380860-8.00003-3
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
The main type of RNA editing in mammals is the conversion of adenosine to inosine which is translated as if it were guanosine. The enzymes that catalyze this reaction are ADARs (adenosine deaminases that act on RNA), of which there are four in mammals, two of which are catalytically inactive. ADARs edit transcripts that encode proteins expressed mainly in the CNS and editing is crucial to maintain a correctly functioning nervous system. However, the majority of editing has been found in transcripts encoding Alu repeat elements and the biological role of this editing remains a mystery. This chapter describes in detail the different ADAR enzymes and the phenotype of animals that are deficient in their activity. Besides being enzymes, ADARs are also double-stranded RNA-binding proteins, so by binding alone they can interfere with other processes such as RNA interference. Lack of editing by ADARs has been implicated in disorders such as forebrain ischemia and Amyotrophic Lateral Sclerosis (ALS) and this will also be discussed. (C) 2011, Elsevier Inc.
引用
收藏
页码:87 / 120
页数:34
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