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

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作者
Petros Marangos
Michelle Stevense
Konstantina Niaka
Michaela Lagoudaki
Ibtissem Nabti
Rolf Jessberger
John Carroll
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[1] UCL,Department of Cell and Developmental Biology, Division of Biosciences
[2] University of Ioannina,Department of Biological Applications and Technology
[3] Institute of Physiological Chemistry,Monash Biomedicine Discovery Institute and Department of Anatomy and Developmental Biology
[4] Faculty of Medicine Carl Gustav Carus,undefined
[5] Dresden University of Technology,undefined
[6] Development and Stem Cells Program,undefined
[7] Monash University,undefined
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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.
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