WANG Hai-yong,ZHANG Xiao-shan,TENG Li-song.Regulation of artemis phosphorylation on replication checkpoint induced by UVC irradiation[J].Chinese Journal of Radiological Medicine and Protection,2009,29(5):543-547
Regulation of artemis phosphorylation on replication checkpoint induced by UVC irradiation
Received:December 23, 2008  
DOI:
KeyWords:Artemis protein  UVC  Phosphorylation  Replication checkpoint  Cell cycle
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Author NameAffiliationE-mail
WANG Hai-yong Department of Oncology, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China  
ZHANG Xiao-shan 美国德克萨斯大学MD Anderson癌症中心  
TENG Li-song Department of Oncology, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China lsteng@hos.zju.edu.cn 
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Abstract::
      Objective To investigate Artemis phosphorylation on S516 and S645 in response to stalled replication forks and its role in regulation of cell cycle replication checkpoint. Methods Western-blotting was used to measure the expression of phosphorylation of Artemis on S516 and S645 after UVC irradiation. The non-phosphorylatable double mutant (S516-645A) and the mimicking phosphorylation mutant (S516-645D) plasmids were constructed. HEK 293 cells with stable expression of wild type Artemis and the corresponding mutants were established by transfection. Cell cycles of the cells treated with UVC irradiation were analyzed by flow cytometry, Western-blotting was used to measure the expression of Chk1,γ-H2AX and Cdk2. IP-kinase assay was used to measure the kinase activity of Cdk2 2, 6 and 12 h after UVC irradiation. Results Artemis got rapid and prolonged phosphorylation on S516 and S645 after treatment with UVC irradiation and the major responsible kinase was ATR. The S516-645A mutant caused prolonged arrest in replication checkpoint in S phase. The Cdk2 IP kinase activity was inhibited in S516-645A mutant cells, but the expression levels of Chk1,Cdk2 and γ-H2AX were not affected. Conclusion\ The ATR phosphorylation on S516 and S645 of Artemis promotes cell cycle recovery from UVC induced replication checkpoint.
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