Bioscience and Biotechnology, School of Advanced Science and Technology, Japan Advanced Institute of Science and Technology (JAIST), 1-1 Asahidai, Nomi City 923-1292, Japan.
Department of Anatomy and Histology, Faculty of Veterinary Science, Bangladesh Agricultural University, Mymensingh 2202, Bangladesh.
Genes (Basel). 2022 Sep 12;13(9):1636. doi: 10.3390/genes13091636.
The restoration of genetic code by editing mutated genes is a potential method for the treatment of genetic diseases/disorders. Genetic disorders are caused by the point mutations of thymine (T) to cytidine (C) or guanosine (G) to adenine (A), for which gene editing (editing of mutated genes) is a promising therapeutic technique. In C-to-Uridine (U) RNA editing, it converts the base C-to-U in RNA molecules and leads to nonsynonymous changes when occurring in coding regions; however, for G-to-A mutations, A-to-I editing occurs. Editing of C-to-U is not as physiologically common as that of A-to-I editing. Although hundreds to thousands of coding sites have been found to be C-to-U edited or editable in humans, the biological significance of this phenomenon remains elusive. In this review, we have tried to provide detailed information on physiological and artificial approaches for C-to-U RNA editing.
通过编辑突变基因来恢复遗传密码是治疗遗传疾病/障碍的一种有潜力的方法。遗传疾病是由胸腺嘧啶(T)突变为胞嘧啶(C)或鸟嘌呤(G)突变为腺嘌呤(A)引起的,对于这些疾病,基因编辑(编辑突变基因)是一种很有前途的治疗技术。在 C 到尿嘧啶(U)的 RNA 编辑中,它将 RNA 分子中的碱基 C 转换为 U,并在发生在编码区时导致非同义突变;然而,对于 G 到 A 的突变,会发生 A 到 I 的编辑。C 到 U 的编辑不如 A 到 I 的编辑在生理上常见。尽管已经在人类中发现了数百到数千个编码位点可以进行 C 到 U 的编辑或可编辑性,但这种现象的生物学意义仍然难以捉摸。在这篇综述中,我们试图提供关于 C 到 U RNA 编辑的生理和人工方法的详细信息。