WIP1 phosphatase suppresses the DNA damage response during G2/prophase arrest in mouse oocytes†
Author:
Affiliation:
1. Department of Integrative Biotechnology, College of Biotechnology and Bioengineering, Sungkyunkwan University, Suwon, South Korea
2. Division of Radiation Cancer Research, Korea Institute of Radiological and Medical Sciences, Seoul, South Korea
Funder
National Research Foundation of Korea
Ministry of Science, ICT and Future Planning
Publisher
Oxford University Press (OUP)
Subject
Cell Biology,General Medicine,Reproductive Medicine
Link
http://academic.oup.com/biolreprod/article-pdf/99/4/798/26181941/ioy108.pdf
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3. The ATM-Chk2 and ATR-Chk1 pathways in DNA damage signaling and cancer;Smith;Adv Cancer Res,2010
4. DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation;Bakkenist;Nature,2003
5. Formation of dynamic gamma-H2AX domains along broken DNA strands is distinctly regulated by ATM and MDC1 and dependent upon H2AX densities in chromatin;Savic;Mol Cell,2009
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3. Oocytes can repair DNA damage during meiosis via a microtubule-dependent recruitment of CIP2A–MDC1–TOPBP1 complex from spindle pole to chromosomes;Nucleic Acids Research;2023-03-31
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