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Publication : WIP1 phosphatase suppresses the DNA damage response during G2/prophase arrest in mouse oocytes.

First Author  Leem J Year  2018
Journal  Biol Reprod Volume  99
Issue  4 Pages  798-805
PubMed ID  29733326 Mgi Jnum  J:266582
Mgi Id  MGI:6220823 Doi  10.1093/biolre/ioy108
Citation  Leem J, et al. (2018) WIP1 phosphatase suppresses the DNA damage response during G2/prophase arrest in mouse oocytes. Biol Reprod 99(4):798-805
abstractText  Maternal DNA damage during meiosis causes genetic abnormalities that can lead to infertility, birth defects, and abortion. While DNA damage can rapidly halt cell cycle progression and promote DNA repair in somatic cells, mammalian oocytes are unable to mount a robust G2/prophase arrest in response to DNA damage unless damage levels are severe. Here, we show that inhibition of WIP1 phosphatase enhances the ability of oocytes to respond to DNA damage. We found that WIP1 was expressed constantly during meiotic maturation, and that inhibition of WIP1 activity did not impair meiotic maturation. However, oocytes in G2/prophase were sensitized to DNA damage following WIP1 inhibition, not only increasing gamma-H2AX level and ATM phosphorylation, but also decreasing entry into meiosis. Moreover, WIP1 inhibition significantly promoted the repair of damaged DNA during G2/prophase arrest, suggesting that WIP1 suppresses DNA repair in oocytes. Therefore, our results suggest that WIP1 is a key suppressor of the DNA damage response during G2/prophase arrest in mouse oocytes.
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