DNA methylation on N6-adenine in mammalian embryonic stem cells

  • Tao P. Wu
  • , Tao Wang
  • , Matthew G. Seetin
  • , Yongquan Lai
  • , Shijia Zhu
  • , Kaixuan Lin
  • , Yifei Liu
  • , Stephanie D. Byrum
  • , Samuel G. Mackintosh
  • , Mei Zhong
  • , Alan Tackett
  • , Guilin Wang
  • , Lawrence S. Hon
  • , Gang Fang
  • , James A. Swenberg
  • , Andrew Z. Xiao

Research output: Contribution to journalArticlepeer-review

542 Scopus citations

Abstract

It has been widely accepted that 5-methylcytosine is the only form of DNA methylation in mammalian genomes. Here we identify N6-methyladenine as another form of DNA modification in mouse embryonic stem cells. Alkbh1 encodes a demethylase for N6-methyladenine. An increase of N6-methyladenine levels in Alkbh1-deficient cells leads to transcriptional silencing. N6-methyladenine deposition is inversely correlated with the evolutionary age of LINE-1 transposons; its deposition is strongly enriched at young (<1.5 million years old) but not old (>6 million years old) L1 elements. The deposition of N6-methyladenine correlates with epigenetic silencing of such LINE-1 transposons, together with their neighbouring enhancers and genes, thereby resisting the gene activation signals during embryonic stem cell differentiation. As young full-length LINE-1 transposons are strongly enriched on the X chromosome, genes located on the X chromosome are also silenced. Thus, N6-methyladenine developed a new role in epigenetic silencing in mammalian evolution distinct from its role in gene activation in other organisms. Our results demonstrate that N6-methyladenine constitutes a crucial component of the epigenetic regulation repertoire in mammalian genomes.

Original languageEnglish (US)
Pages (from-to)329-333
Number of pages5
JournalNature
Volume532
Issue number7599
DOIs
StatePublished - Apr 21 2016

All Science Journal Classification (ASJC) codes

  • General

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