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CDK1 Regulates Mediator of DNA Damage Checkpoint 1 during Mitotic DNA Damage
Author(s) -
Bing Yu,
W. Brian Dalton,
Vincent W. Yang
Publication year - 2012
Publication title -
cancer research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.103
H-Index - 449
eISSN - 1538-7445
pISSN - 0008-5472
DOI - 10.1158/0008-5472.can-12-2354
Subject(s) - g2 m dna damage checkpoint , dna damage , mitosis , chek1 , mediator , microbiology and biotechnology , cyclin dependent kinase 1 , dna , biology , cancer research , cell cycle checkpoint , genetics , cell cycle , cancer
Cells engage sophisticated programs of DNA damage response (DDR) and repair to guard against genetic mutations. Although there is significant knowledge concerning DDR in interphase cells, much less is known about these processes in mitosis. Direct interaction between MDC1, a master DDR organizer, and a marker of DNA damage, histone γH2AX, is required to trigger robust repair. Here we show that the DNA damage-induced interaction between MDC1 and γH2AX is attenuated in mitosis. Furthermore, inhibition in the activity of the core mitotic regulator CDK1, either by pharmacologic inhibition or siRNA attenuation, enhances MDC1-γH2AX colocalization in mitosis. Our findings offer key new insights into how DDR is controlled during mitosis.

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