Nature Communications (Aug 2022)

Histone H3K36me2 and H3K36me3 form a chromatin platform essential for DNMT3A-dependent DNA methylation in mouse oocytes

  • Seiichi Yano,
  • Takashi Ishiuchi,
  • Shusaku Abe,
  • Satoshi H. Namekawa,
  • Gang Huang,
  • Yoshihiro Ogawa,
  • Hiroyuki Sasaki

DOI
https://doi.org/10.1038/s41467-022-32141-2
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 12

Abstract

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DNMT3A is known to methylate DNA at histone H3 lysine 36 (H3K36me3)-marked transcriptionally active regions in mouse oocytes. Here the authors show that DNMT3A is also guided by H3K36me2 to methylate broad domains in genic and intergenic loci, as well as on the X chromosome. These two histone marks together comprise the minimal chromatin signature for global DNA methylation in mouse oocytes.