Training Program in Neuroscience, Vanderbilt University, Nashville, TN 37232, USA.
Department of Chemistry, University of California, Davis, Davis, CA 95616, USA.
Nucleic Acids Res. 2021 Apr 19;49(7):4020-4036. doi: 10.1093/nar/gkab157.
The hydrolytic deamination of adenosine-to-inosine (A-to-I) by RNA editing is a widespread post-transcriptional modification catalyzed by the adenosine deaminase acting on RNA (ADAR) family of proteins. ADAR-mediated RNA editing modulates cellular pathways involved in innate immunity, RNA splicing, RNA interference, and protein recoding, and has been investigated as a strategy for therapeutic intervention of genetic disorders. Despite advances in basic and translational research, the mechanisms regulating RNA editing are poorly understood. Though several trans-acting regulators of editing have been shown to modulate ADAR protein expression, previous studies have not identified factors that modulate ADAR catalytic activity. Here, we show that RNA editing increases upon intracellular acidification, and that these effects are predominantly explained by both enhanced ADAR base-flipping and deamination rate at acidic pH. We also show that the extent of RNA editing increases with the reduction in pH associated with conditions of cellular hypoxia.
RNA 编辑介导的腺苷酸水解脱氨(A 到 I)是一种广泛存在的转录后修饰,由腺苷脱氨酶作用于 RNA(ADAR)家族蛋白催化。ADAR 介导的 RNA 编辑调节参与固有免疫、RNA 剪接、RNA 干扰和蛋白质重编码的细胞途径,并已被研究作为治疗遗传疾病的策略。尽管在基础和转化研究方面取得了进展,但 RNA 编辑的调控机制仍知之甚少。尽管已经证明了几种 RNA 编辑的反式作用调节剂可以调节 ADAR 蛋白的表达,但以前的研究尚未确定调节 ADAR 催化活性的因素。在这里,我们表明细胞内酸化会增加 RNA 编辑,并且这些影响主要是通过增强 ADAR 碱基翻转和酸性 pH 下脱氨速率来解释的。我们还表明,随着与细胞缺氧相关的 pH 值降低,RNA 编辑的程度增加。