Kudriavskii Viacheslav V, Kliuchnikova Anna A, Goncharov Anton O, Ilgisonis Ekaterina V, Moshkovskii Sergei A
Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, 119435 Moscow, Russia.
Biochemistry Department, School of Biomedicine, Pirogov Russian National Research Medical University, 117997 Moscow, Russia.
Int J Mol Sci. 2025 Jul 16;26(14):6837. doi: 10.3390/ijms26146837.
This paper summarizes the results of multi-year studies performed by our research team, focusing on an analysis of protein recoding mediated by messenger RNA editing by ADAR adenosine deaminases. Searching for ADAR-mediated protein recoding was performed in the central nervous system of the model organisms, fruit fly and mouse, as well as in the human proteomic datasets. The proteogenomic approach has made it possible to identify dozens of editing events in the proteome, thus validating the results of transcriptomic studies. The observed recoding events in animals, ranging from insects to mammals, mainly affect the cytoskeletal components and proteins involved in synaptic transmission. In humans, recoding changes are most often observed in the central nervous system or tumor tissues. Over 15 million editing sites have been identified in humans; only a few thousand of those can potentially yield amino acid substitutions. Using a proteogenomic approach, dozens of protein recoding sites are identified, demonstrating their origin in ADAR RNA editing. Moreover, this revealed that the level of recoding at specific sites is not directly related to the abundance of ADAR enzymes per se or their target proteins. The recoding processes probably have differential regulation of interactions at the mRNA level that is yet to be clarified.
本文总结了我们研究团队多年来的研究成果,重点分析了由ADAR腺苷脱氨酶介导的信使核糖核酸编辑所介导的蛋白质重新编码。在模式生物果蝇和小鼠的中枢神经系统以及人类蛋白质组数据集中搜索ADAR介导的蛋白质重新编码。蛋白质基因组学方法使得在蛋白质组中识别数十种编辑事件成为可能,从而验证了转录组学研究的结果。在从昆虫到哺乳动物的动物中观察到的重新编码事件,主要影响细胞骨架成分和参与突触传递的蛋白质。在人类中,重新编码变化最常出现在中枢神经系统或肿瘤组织中。在人类中已经鉴定出超过1500万个编辑位点;其中只有几千个可能产生氨基酸替换。使用蛋白质基因组学方法,鉴定出了数十个蛋白质重新编码位点,证明了它们起源于ADAR RNA编辑。此外,这表明特定位点的重新编码水平与ADAR酶本身或其靶蛋白的丰度没有直接关系。重新编码过程可能在mRNA水平上具有尚未阐明的相互作用的差异调节。