DNA damage-induced metaphase I arrest is mediated by the spindle assembly checkpoint and maternal age

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Petros Marangos - , Max Planck Institute for Molecular Biomedicine (Author)
  • Michelle Stevense - , Institute of Physiological Chemistry (Author)
  • Konstantina Niaka - , University of Ioannina (Author)
  • Michaela Lagoudaki - , University of Ioannina (Author)
  • Ibtissem Nabti - , Max Planck Institute for Molecular Biomedicine (Author)
  • Rolf Jessberger - , Institute of Physiological Chemistry (Author)
  • John Carroll - , Max Planck Institute for Molecular Biomedicine (Author)

Abstract

In mammalian oocytes DNA damage can cause chromosomal abnormalities that potentially lead to infertility and developmental disorders. However, there is little known about the response of oocytes to DNA damage. Here we find that oocytes with DNA damage arrest at metaphase of the first meiosis (MI). The MI arrest is induced by the spindle assembly checkpoint (SAC) because inhibiting the SAC overrides the DNA damage-induced MI arrest. Furthermore, this MI checkpoint is compromised in oocytes from aged mice. These data lead us to propose that the SAC is a major gatekeeper preventing the progression of oocytes harbouring DNA damage. The SAC therefore acts to integrate protection against both aneuploidy and DNA damage by preventing production of abnormal mature oocytes and subsequent embryos. Finally, we suggest escaping this DNA damage checkpoint in maternal ageing may be one of the causes of increased chromosome anomalies in oocytes and embryos from older mothers.

Details

Original languageEnglish
Article number8706
JournalNature Communications
Volume6
Publication statusPublished - 2 Nov 2015
Peer-reviewedYes

External IDs

Scopus 84946202576
PubMed 26522734
PubMedCentral PMC4667640

Keywords

Keywords

  • Animals, DNA Damage, Female, M Phase Cell Cycle Checkpoints, Maternal Age, Meiosis, Metaphase, Mice, Mice, Inbred C57BL, Oocytes/cytology, Pregnancy