EPC1/TIP60-mediated histone acetylation facilitates spermiogenesis in mice

Yixin Dong*, Kyo Ichi Isono, Kazuyuki Ohbo, Takaho A. Endo, Osamu Ohara, Mamiko Maekawa, Yoshiro Toyama, Chizuru Ito, Kiyotaka Toshimori, Kristian Helin, Narumi Ogonuki, Kimiko Inoue, Atsuo Ogura, Kazutsune Yamagata, Issay Kitabayashi, Haruhiko Koseki

*Corresponding author for this work
12 Citations (Scopus)

Abstract

Global histone hyperacetylation is suggested to play a critical role for replacement of histones by transition proteins and protamines to compact the genome during spermiogenesis. However, the underlying mechanisms for hyperacetylation- mediated histone replacement remains poorly understood. Here, we report that EPC1 and TIP60, two critical components of the mammalian nucleosome acetyltransferase of H4 (NuA4) complexes, are coexpressed in male germ cells. Strikingly, genetic ablation of either Epc1 or Tip60 disrupts hyperacetylation and impairs histone replacement, in turn causing aberrant spermatid development. Taking these observations together, we reveal an essential role of the NuA4 complexes for histone hyperacetylation and subsequent compaction of the spermatid genome.

Original languageEnglish
Article numbere00082-17
JournalMolecular and Cellular Biology
Volume37
Issue number19
Number of pages16
ISSN0270-7306
DOIs
Publication statusPublished - 1 Oct 2017

Keywords

  • EPC1
  • Histone acetylation
  • Mouse
  • Spermatids
  • Spermiogenesis
  • TIP60

Fingerprint

Dive into the research topics of 'EPC1/TIP60-mediated histone acetylation facilitates spermiogenesis in mice'. Together they form a unique fingerprint.

Cite this