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

机译:DNA损伤诱导的中期I阻滞由纺锤体装配检查点和产妇年龄介导

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摘要

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.
机译:在哺乳动物卵母细胞中,DNA损伤会导致染色体异常,从而可能导致不育和发育障碍。然而,关于卵母细胞对DNA损伤的反应知之甚少。在这里,我们发现具有DNA损伤的卵母细胞停在第一个减数分裂(MI)的中期。 MI停止由主轴组件检查点(SAC)引起,因为抑制SAC会覆盖DNA损伤引起的MI停止。此外,该MI检查点在老年小鼠的卵母细胞中受损。这些数据使我们提出,SAC是防止携带DNA损伤的卵母细胞进展的主要守门人。因此,SAC通过防止异常成熟的卵母细胞和后续胚胎的产生来整合针对非整倍性和DNA损伤的保护。最后,我们建议逃脱孕妇衰老中的DNA损伤检查点可能是年长母亲的卵母细胞和胚胎中染色体异常增加的原因之一。

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