Regulation of histone acetylation during meiotic maturation in mouse oocytes

Tomohiko Akiyama, Jin Moon Kim, Masao Nagata, Fugaku Aoki

Research output: Contribution to journalArticlepeer-review

73 Citations (Scopus)


Histone acetylation is an important epigenetic modification implicated in the regulation of chromatin structure and, subsequently, gene expression. Global histone deacetylation was reported in mouse oocytes during meiosis but not mitosis. The regulation of this meiosis-specific deacetylation has not been elucidated. Here, we demonstrate that p34cdc2 kinase activity and protein synthesis are responsible for the activation of histone deacetylases and the inhibition of histone acetyltransferases (HATs), respectively, resulting in deacetylation of histone H4 at lysine-12 (H4K12) during mouse oocyte meiosis. Temporal changes in the acetylation state of H4K12 were examined immunocytochemically during meiotic maturation using an antibody specific for acetylated H4K12. H4K12 was deacetylated during the first meiosis, temporarily acetylated around the time of the first polar body (PB1) extrusion, and then deacetylated again during the second meiosis. Because these changes coincided with the known oscillation pattern of p34cdc2 kinase activity, we investigated the involvement of the kinase in H4K12 deacetylation. Roscovitine, an inhibitor of cyclin-dependent kinase activity, prevented H4K12 deacetylation during both the first and second meiosis, suggesting that p34cdc2 kinase activity is required for deacetylation during meiosis. In addition, cycloheximide, a protein synthesis inhibitor, also prevented deacetylation. After PB1 extrusion, at which time H4K12 had been deacetylated, H4K12 was re-acetylated in the condensed chromosomes by treatment with cycloheximide but not with roscovitine. These results demonstrate that HATs are present but inactivated by newly synthesized protein(s) that is (are) not involved in p34cdc2 kinase activity. Our results suggest that p34cdc2 kinase activity induces the deacetylation of H4K12 and that the deacetylated state is maintained by newly synthesized protein(s) that inhibits HAT activity during meiosis.

Original languageEnglish
Pages (from-to)222-227
Number of pages6
JournalMolecular reproduction and development
Issue number2
Publication statusPublished - 2004 Oct
Externally publishedYes


  • Acetylation
  • Deacetylation
  • Histone
  • Oocyte, p34

ASJC Scopus subject areas

  • Genetics
  • Developmental Biology
  • Cell Biology


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