Literature DB >> 32183942

N6-Deoxyadenosine Methylation in Mammalian Mitochondrial DNA.

Ziyang Hao1, Tong Wu1, Xiaolong Cui1, Pingping Zhu2, Caiping Tan3, Xiaoyang Dou1, Kai-Wen Hsu4, Yueh-Te Lin4, Pei-Hua Peng4, Li-Sheng Zhang1, Yawei Gao5, Lulu Hu1, Hui-Lung Sun1, Allen Zhu1, Jianzhao Liu1, Kou-Juey Wu4, Chuan He6.   

Abstract

N6-Methyldeoxyadenosine (6mA) has recently been shown to exist and play regulatory roles in eukaryotic genomic DNA (gDNA). However, the biological functions of 6mA in mammals have yet to be adequately explored, largely due to its low abundance in most mammalian genomes. Here, we report that mammalian mitochondrial DNA (mtDNA) is enriched for 6mA. The level of 6mA in HepG2 mtDNA is at least 1,300-fold higher than that in gDNA under normal growth conditions, corresponding to approximately four 6mA modifications on each mtDNA molecule. METTL4, a putative mammalian methyltransferase, can mediate mtDNA 6mA methylation, which contributes to attenuated mtDNA transcription and a reduced mtDNA copy number. Mechanistically, the presence of 6mA could repress DNA binding and bending by mitochondrial transcription factor (TFAM). Under hypoxia, the 6mA level in mtDNA could be further elevated, suggesting regulatory roles for 6mA in mitochondrial stress response. Our study reveals DNA 6mA as a regulatory mark in mammalian mtDNA.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  METTL4; N(6)-methyldeoxyadenosine (6mA); TFAM; methyltransferase; mitochondrial DNA methylation; mitochondrial replication; mitochondrial transcription regulation

Mesh:

Substances:

Year:  2020        PMID: 32183942      PMCID: PMC7214128          DOI: 10.1016/j.molcel.2020.02.018

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  72 in total

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