Ohman M
Department of Molecular Biology and Functional Genomics, Stockholm University, S-106 91 Stockholm, Sweden.
Biochimie. 2007 Oct;89(10):1171-6. doi: 10.1016/j.biochi.2007.06.002. Epub 2007 Jun 8.
Adenosine to inosine (A-to-I) modification by the ADAR (adenosine deaminase that acts on RNA) enzymes perform the most common type of RNA editing in metazoans. ADARs use double stranded RNA as substrates but allow interruptions of bulges and loops in the structure. It is well known that these enzymes can use messenger RNA as targets for A-to-I editing and thereby recode the transcript. Both ADAR1 and ADAR2 have been proven to be able to also target short double stranded RNA molecules of the same size as a microRNA. However, it is not until recently shown that A-to-I editing occurs in microRNAs and its precursors. Since the editing activity is found both in the nucleus and the cytoplasm there are several steps during the microRNA maturation pathway that can be targeted for modification. This review will give an overview of what is known today about the interactions between the endogenous RNA interference process and RNA editing. It will also give some insight into the power of A-to-I modification in its ability to increase the variety of microRNA gene silencing.
由ADAR(作用于RNA的腺苷脱氨酶)酶催化的腺苷到肌苷(A-to-I)修饰是后生动物中最常见的RNA编辑类型。ADARs以双链RNA为底物,但允许结构中存在凸起和环的中断。众所周知,这些酶可以将信使RNA作为A-to-I编辑的靶标,从而对转录本进行重新编码。ADAR1和ADAR2都已被证明也能够靶向与微小RNA大小相同的短双链RNA分子。然而,直到最近才发现A-to-I编辑发生在微小RNA及其前体中。由于编辑活性在细胞核和细胞质中均有发现,因此在微小RNA成熟途径中有几个步骤可作为修饰的靶点。本综述将概述目前已知的内源性RNA干扰过程与RNA编辑之间的相互作用。它还将深入探讨A-to-I修饰在增加微小RNA基因沉默多样性方面的作用。