a State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, College of Animal Science and Technology, Guangxi University , Nanning , P.R. China.
b Center for Genome Analysis, ABLife Inc ., Wuhan , Hubei , China.
RNA Biol. 2019 Sep;16(9):1179-1189. doi: 10.1080/15476286.2019.1621120. Epub 2019 May 31.
-methyladenosine (mA) is considered as a reversible RNA modification occurring more frequently on the GAC than AAC context , which regulates post-transcriptional gene expression in mammalian cells. mA 'writers' METTL3 and METTL14 demonstrate a strong preference for binding AC-containing motifs in living cells. However, this evidence is currently lacking for mA erasers, leaving the dynamics of the internal mA modification under debate recently. We analysed three recently published FTO CLIP-seq data sets and two generated in this study, one of the two known mA 'erasers'. FTO binding peaks from all cell lines contain RRACH motifs. Only those from K562, 3T3-L1and HeLa cells were enriched in AC-containing motifs, while those from HEK293 were not. The exogenously overexpressed FTO effectively binds to mA motif-containing RNA sites. FTO overexpression specifically removed mA modification from GGACU and RRACU motifs in a concentration-dependent manner. These findings underline the dynamics of FTO in target selection, which is predicted to contribute to both the mA dynamics and the FTO plasticity in biological functions and diseases.
m6A(甲基腺嘌呤)被认为是一种在 GAC 而非 AAC 环境中更频繁发生的 RNA 可逆修饰,它调节哺乳动物细胞中的转录后基因表达。m6A“写入器”METTL3 和 METTL14 在活细胞中表现出对 AC 富含基序的强烈偏好。然而,目前缺乏对 m6A 擦除器的证据,这使得内部 m6A 修饰的动态最近受到争议。我们分析了三个最近发表的 FTO CLIP-seq 数据集和两个本研究生成的数据集,其中一个是两个已知的 m6A“擦除器”之一。所有细胞系的 FTO 结合峰都包含 RRACH 基序。只有 K562、3T3-L1 和 HeLa 细胞的结合峰富含 AC 富含基序,而 HEK293 的则没有。外源性过表达的 FTO 有效地结合到含有 m6A 基序的 RNA 位点。FTO 过表达特异性地以浓度依赖的方式从 GGACU 和 RRACU 基序中去除 m6A 修饰。这些发现强调了 FTO 在靶标选择中的动态性,这预计有助于 m6A 动态性以及 FTO 在生物学功能和疾病中的可塑性。