|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
45
|
|
pubmed:dateCreated |
2004-11-1
|
|
pubmed:abstractText |
DNA damage initiates signaling events through kinase cascades that result in cell cycle checkpoint control and DNA repair. However, it is not yet clear how the signaling pathways relay to DNA damage repair. Using the repeat region of checkpoint protein MDC1 (mediator of DNA damage checkpoint protein 1), we identified DNA-PKcs/Ku as MDC1-associated proteins. Here, we show that MDC1 directly interacts with the Ku/DNA-PKcs complex. Down-regulation of MDC1 resulted in defective phospho-DNA-PKcs foci formation and DNA-PKcs autophosphorylation, suggesting that MDC1 regulates autophosphorylation of DNA-PKcs following DNA damage. Furthermore, DNA-PK-dependent DNA damage repair is defective in cells depleted of MDC1. Taken together, these results suggest that the MDC1 repeat region is involved in protein-protein interaction with DNA-PKcs/Ku, and MDC1 regulates DNA damage repair by influencing DNA-PK autophosphorylation. Therefore, MDC1 acts not only as a mediator of DNA damage checkpoint but also as a mediator of DNA damage repair.
|
|
pubmed:grant |
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Activated Protein Kinase,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione Transferase,
http://linkedlifedata.com/resource/pubmed/chemical/MDC1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/PRKDC protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Small Interfering,
http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Nov
|
|
pubmed:issn |
0021-9258
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:day |
5
|
|
pubmed:volume |
279
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
46359-62
|
|
pubmed:dateRevised |
2009-11-19
|
|
pubmed:meshHeading |
pubmed-meshheading:15377652-Cell Cycle,
pubmed-meshheading:15377652-Cell Line,
pubmed-meshheading:15377652-DNA,
pubmed-meshheading:15377652-DNA Damage,
pubmed-meshheading:15377652-DNA Repair,
pubmed-meshheading:15377652-DNA-Activated Protein Kinase,
pubmed-meshheading:15377652-DNA-Binding Proteins,
pubmed-meshheading:15377652-Down-Regulation,
pubmed-meshheading:15377652-Glutathione Transferase,
pubmed-meshheading:15377652-HeLa Cells,
pubmed-meshheading:15377652-Humans,
pubmed-meshheading:15377652-Microscopy, Fluorescence,
pubmed-meshheading:15377652-Nuclear Proteins,
pubmed-meshheading:15377652-Phosphorylation,
pubmed-meshheading:15377652-Protein Binding,
pubmed-meshheading:15377652-Protein Structure, Tertiary,
pubmed-meshheading:15377652-Protein-Serine-Threonine Kinases,
pubmed-meshheading:15377652-RNA, Small Interfering,
pubmed-meshheading:15377652-Trans-Activators,
pubmed-meshheading:15377652-Transfection
|
|
pubmed:year |
2004
|
|
pubmed:articleTitle |
MDC1 regulates DNA-PK autophosphorylation in response to DNA damage.
|
|
pubmed:affiliation |
Department of Oncology, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.
|
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
|
