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The role of mRNA m 6 A methylation in the nervous system

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TLDR
The research progress and related mechanisms of the role of mRNA m6A methylation in the nervous system from the aspects of neural stem cells, learning and memory, brain development, axon growth and glioblastoma are reviewed.
Abstract
Epitranscriptomics, also known as “RNA epigenetics”, is a chemical modification for RNA regulation. Ribonucleic acid (RNA) methylation is considered to be a major discovery following the deoxyribonucleic acid (DNA) and histone methylation. Messenger RNA (mRNA) methylation modification accounts for more than 60% of all RNA modifications and N6-methyladenosine (m6A) is known as one of the most common type of eukaryotic mRNA methylation modifications in current. The m6A modification is a dynamic reversible modification, which can directly or indirectly affect biological processes, such as RNA degradation, translation and splicing, and can play important biological roles in vivo. This article introduces the mRNA m6A methylation modification enzymes and binding proteins, and reviews the research progress and related mechanisms of the role of mRNA m6A methylation in the nervous system from the aspects of neural stem cells, learning and memory, brain development, axon growth and glioblastoma.

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Journal ArticleDOI

The role of m6A modification in the biological functions and diseases.

TL;DR: In this paper, the authors discuss how m6A RNA methylation influences both the physiological and pathological progressions of hematopoietic, central nervous and reproductive systems.
Journal ArticleDOI

Landscape and Regulation of m6A and m6Am Methylome across Human and Mouse Tissues

TL;DR: The m6A and m6Am methylome is reported through profiling of 43 human and 16 mouse tissues and demonstrates strongest tissue specificity for the brain tissues and cross-species analysis revealed that species rather than tissue type is the primary determinant of methylation.
Journal ArticleDOI

The role of N 6 -methyladenosine (m 6 A) modification in the regulation of circRNAs

TL;DR: The role of m6A modification in the regulation and function of circRNAs is summarized and the potential applications and possible future directions in the field are discussed.
Journal ArticleDOI

The mechanism of m 6 A methyltransferase METTL3-mediated autophagy in reversing gefitinib resistance in NSCLC cells by β-elemene

TL;DR: The mechanism of METTL3-mediated autophagy in reversing gefitinib resistance of NSCLC cells by β-elemene is unveiled, which shed light on providing potential molecular-therapy target and clinical-treatment method in NSclC patients with gefitsinib resistant cells.
Journal ArticleDOI

Function and evolution of RNA N6-methyladenosine modification.

TL;DR: Accumulating evidence shows that m6A RNA methylation participates in almost all aspects of RNA processing, implying an association with important bioprocesses.
References
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Journal ArticleDOI

Comprehensive Analysis of mRNA Methylation Reveals Enrichment in 3′ UTRs and near Stop Codons

TL;DR: A method is presented for transcriptome-wide m(6)A localization, which combines m( 6)A-specific methylated RNA immunoprecipitation with next-generation sequencing (MeRIP-Seq) and reveals insights into the epigenetic regulation of the mammalian transcriptome.
Journal ArticleDOI

N6-methyladenosine in nuclear RNA is a major substrate of the obesity-associated FTO.

TL;DR: FTO exhibits efficient oxidative demethylation activity of abundant N6-methyladenosine (m6A) residues in RNA in vitro, and it is shown that FTO partially colocalizes with nuclear speckles, supporting m6A in nuclear RNA as a physiological substrate of FTO.
Journal ArticleDOI

N6-methyladenosine Modulates Messenger RNA Translation Efficiency

TL;DR: In a unified mechanism of m(6)A-based regulation in the cytoplasm, YTHDF2-mediated degradation controls the lifetime of target transcripts, whereasYTHDF1-mediated translation promotion increases translation efficiency, ensuring effective protein production from dynamic transcripts that are marked by m( 6)A.
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