m6A in the Signal Transduction Network

被引:22
|
作者
Jang, Ki-Hong [1 ]
Heras, Chloe R. [1 ,2 ]
Lee, Gina [1 ]
机构
[1] Univ Calif Irvine, Sch Med, Dept Microbiol & Mol Genet, Chao Family Comprehens Canc Ctr, Irvine, CA 92617 USA
[2] Univ Calif Irvine, Sch Biol Sci, Irvine, CA 92697 USA
关键词
ERK; mTOR; N-6-methyladenosine; RNA modification; signaling; TGF; MESSENGER-RNA METHYLATION; STRUCTURAL BASIS; MOLECULAR-MECHANISMS; DEMETHYLASE ALKBH5; HELICASE YTHDC2; CELL-GROWTH; NUCLEAR-RNA; TRANSLATION; BINDING; PROTEIN;
D O I
10.14348/molcells.2022.0017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In response to environmental changes, signaling pathways rewire gene expression programs through transcription factors. Epigenetic modification of the transcribed RNA can be another layer of gene expression regulation. N6 adenosine methylation (m6A) is one of the most common modifications on mRNA. It is a reversible chemical mark catalyzed by the enzymes that deposit and remove methyl groups. m6A recruits effector proteins that determine the fate of mRNAs through changes in splicing, cellular localization, stability, and translation efficiency. Emerging evidence shows that key signal transduction pathways including TGF?? (transforming growth factor-??), ERK (extracellular signal-regulated kinase), and mTORC1 (mechanistic target of rapamycin complex 1) regulate downstream gene expression through m6A processing. Conversely, m6A can modulate the activity of signal transduction networks via m6A modification of signaling pathway genes or by acting as a ligand for receptors. In this review, we discuss the current understanding of the crosstalk between m6A and signaling pathways and its implication for biological systems.
引用
收藏
页码:435 / 443
页数:9
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