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可卡因条件性小鼠海马中差异m6A RNA甲基化组的综合分析

Comprehensive Analysis of Differential m6A RNA Methylomes in the Hippocampus of Cocaine-Conditioned Mice.

作者信息

Xue Aiqin, Huang Yan, Li Meng, Wei Qian, Bu Qian

机构信息

West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, 610041, China.

National Chengdu Center for Safety Evaluation of Drugs, State Key Lab of Biotherapy/Collaborative Innovation Center of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, 610041, China.

出版信息

Mol Neurobiol. 2021 Aug;58(8):3759-3768. doi: 10.1007/s12035-021-02363-4. Epub 2021 Apr 7.

Abstract

N6-methyladenosine (m6A) is the most prevalent internal modification found in mRNAs and lncRNA and plays a vital role in posttranscriptional regulation in mammals. m6A is abundant in the nervous system, where it modulates neuronal development and hippocampus-dependent learning and memory. However, the roles of RNAs m6A modification and its related enzymes in cocaine reward are still not fully understood. In this study, we found that the fat mass and obesity-associated gene (FTO) demethylase, but not methyltransferase-like 3 (METTL3) and 14 (METTL14), was downregulated in the hippocampus following cocaine-induced conditioned place preference (CPP), and the level of m6A is notably higher in the hippocampus of cocaine CPP training mice. Using methylated m6A RNA immunoprecipitation sequencing (MeRIP-m6A-seq), we identified a total of 6516 m6A peaks within 4460 mRNAs, and 3083 m6A peaks within 850 lncRNAs were significantly dysregulated. Intriguingly, the altered m6A peaks within mRNAs and lncRNAs were enriched in synapse maturation and localization processes. Our study uncovers a critical role for an m6A epitranscriptomic dysregulation and downregulation of FTO expression in the hippocampus following cocaine-induced CPP.

摘要

N6-甲基腺苷(m6A)是在mRNA和lncRNA中发现的最普遍的内部修饰,在哺乳动物的转录后调控中起着至关重要的作用。m6A在神经系统中含量丰富,在其中调节神经元发育以及海马体依赖的学习和记忆。然而,RNA的m6A修饰及其相关酶在可卡因奖赏中的作用仍未完全明确。在本研究中,我们发现,在可卡因诱导的条件性位置偏爱(CPP)后,海马体中的脂肪量和肥胖相关基因(FTO)去甲基化酶表达下调,而甲基转移酶样3(METTL3)和14(METTL14)表达未下调,并且在可卡因CPP训练小鼠的海马体中m6A水平显著更高。使用甲基化m6A RNA免疫沉淀测序(MeRIP-m6A-seq),我们在4460个mRNA中总共鉴定出6516个m6A峰,在850个lncRNA中鉴定出3083个m6A峰存在显著失调。有趣的是,mRNA和lncRNA中改变的m6A峰在突触成熟和定位过程中富集。我们的研究揭示了在可卡因诱导的CPP后,m6A表观转录组失调以及海马体中FTO表达下调的关键作用。

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