Department of Biological Sciences, Lehigh University, Bethlehem, PA, USA.
Biochem Biophys Res Commun. 2011 Sep 2;412(3):407-12. doi: 10.1016/j.bbrc.2011.07.075. Epub 2011 Aug 2.
RNA editing by adenosine deamination, catalyzed by adenosine deaminases acting on RNA (ADAR), is a post-transcriptional modification that contributes to transcriptome and proteome diversity and is widespread in mammals. Here we administer a bioinformatics search strategy to the human and mouse genomes to explore the landscape of A-to-I RNA editing. In both organisms we find evidence for high excess of A/G-type discrepancies (inosine appears as a guanosine in cloned cDNA) at non-polymorphic, non-synonymous codon sites over other types of discrepancies, suggesting the existence of several thousand recoding editing sites in the human and mouse genomes. We experimentally validate recoding-type A-to-I RNA editing in a number of human genes with high scoring positions including the coatomer protein complex subunit alpha (COPA) as well as cyclin dependent kinase CDK13.
RNA 编辑由腺苷脱氨酶催化,该酶作用于 RNA(ADAR),是一种转录后修饰,有助于转录组和蛋白质组的多样性,在哺乳动物中广泛存在。在这里,我们对人类和小鼠基因组进行了生物信息学搜索策略,以探索 A 到 I RNA 编辑的全景。在这两种生物中,我们发现证据表明,在非多态性、非同义密码子位点,A/G 型差异(次黄嘌呤出现在克隆 cDNA 的鸟嘌呤中)比其他类型的差异存在过高的过剩,表明在人类和小鼠基因组中存在几千个重编码编辑位点。我们在包括衣壳蛋白复合物亚基α(COPA)和细胞周期蛋白依赖性激酶 CDK13 在内的许多具有高得分位置的人类基因中实验验证了重编码型 A 到 I RNA 编辑。