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Volume 31, No 1, Jan 2021

ISSN: 1001-0602 
EISSN: 1748-7838 2018 
impact factor 17.848* 
(Clarivate Analytics, 2019)

Volume 31 Issue 1, January 2021: 94-97   |  Open Access

LETTERS TO THE EDITOR

N6-methyladenine is incorporated into mammalian genome by DNA polymerase

Xiaoling Liu1,† , Weiyi Lai1,† , Yao Li1,2,† , Shaokun Chen2 , Baodong Liu1 , Ning Zhang1 , Jiezhen Mo1,2 , Cong Lyu1,2 , Jing Zheng1,2 , Ya-Rui Du3 , Guibin Jiang1 , Guo-Liang Xu3 , Hailin Wang1,2,4,*

1State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China;
2University of Chinese Academy of Sciences, Beijing 100049, China;
3State Key Laboratory of Molecular Biology, Center for Excellence in Molecular Cell Science/Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai 200031, China
4Institute of Environment and Health, Jianghan University, Wuhan, Hubei 430056, China
These authors contributed equally
Correspondence: Hailin Wang(hlwang@rcees.ac.cn)

Dear Editor,

DNA N6-methyladenine (6mA), one of the most prevalent epigenetic base modifications in prokaryotes,1 is recently found in multicellular eukaryotes.2,3,4,5,6,7,8 This nucleobase may have epigenetic roles in regulation of retrotransposons, chromatin organization, and so on.2,3,4,5,6,7,8 However, both our group9 and Greer’s group10 noticed that eukaryotic DNA is easily contaminated with a minute of bacterial DNA, which carries overwhelmingly abundant 6mA (~2% 6mA/dA).1 This brings great challenges for accurate detection of DNA 6mA in eukaryotes in terms of both sample pretreatments and analytical technologies.9,10 For example, inconsistent with the report of Wu et al.,8 Schiffers et al. failed to detect 6mA above background levels in mouse embryonic stem (mES) cells using sensitive ultra-high-performance liquid chromatography-quadruple mass spectrometry (UHPLC-MS/MS) analysis.11 To date, it is of intensive interest to seek conclusive evidence to support the prevalence of this post-replicative adenine modification in mammals.



https://doi.org/10.1038/s41422-020-0317-6

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