| Literature DB >> 29304330 |
Jian-Feng Xiang1, Qin Yang2, Chu-Xiao Liu3, Man Wu4, Ling-Ling Chen5, Li Yang6.
Abstract
N6-methyladenosine (m6A) and adenosine-to-inosine (A-to-I) editing are two of the most abundant RNA modifications, both at adenosines. Yet, the interaction of these two types of adenosine modifications is largely unknown. Here we show a global A-to-I difference between m6A-positive and m6A-negative RNA populations. Both the presence and extent of A-to-I sites in m6A-negative RNA transcripts suggest a negative correlation between m6A and A-to-I. Suppression of m6A-catalyzing enzymes results in global A-to-I RNA editing changes. Further depletion of m6A modification increases the association of m6A-depleted transcripts with adenosine deaminase acting on RNA (ADAR) enzymes, resulting in upregulated A-to-I editing on the same m6A-depleted transcripts. Collectively, the effect of m6A on A-to-I suggests a previously underappreciated interplay between two distinct and abundant RNA modifications, highlighting a complex epitranscriptomic landscape.Entities:
Keywords: A-to-I; ADAR; Alu; N(6)-methyladenosines; RNA editing; RNA modification; RNA structure; m(6)A; m(6)A enzymes
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Year: 2018 PMID: 29304330 DOI: 10.1016/j.molcel.2017.12.006
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970