核糖核酸
亚基因组mRNA
引导RNA
非编码RNA
基因组编辑
遗传学
人类基因组
RNA剪接
作者
Amos A. Schaffer,Erez Y. Levanon
出处
期刊:Methods in molecular biology
日期:2020-07-30
卷期号:: 149-162
被引量:11
标识
DOI:10.1007/978-1-0716-0787-9_9
摘要
Alu elements are repetitive short interspersed elements prevalent in the primate genome. These repeats account for over 10% of the genome with more than a million highly similar copies. A direct outcome of this is an enrichment in long structures of stable dsRNA, which are the target of adenosine deaminases acting on RNAs (ADARs), the enzymes catalyzing A-to-I RNA editing. Indeed, A-to-I editing by ADARs is extremely abundant in primates: over a hundred million editing sites exist in their genomes. However, despite the radical increase in ADAR targets brought on by the introduction of Alu elements, the few evolutionary conserved editing sites manage to retain their editing levels. Here, we review and discuss the cost of having an unusual amount of dsRNA and editing in the transcriptome, as well as the opportunities it presents, which possibly contributed to accelerating primate evolution.
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