Regulators of cyclin-dependent kinases are crucial for maintaining genome integrity in S phase

Author:

Beck Halfdan1,Nähse Viola2,Larsen Marie Sofie Yoo1,Groth Petra3,Clancy Trevor2,Lees Michael1,Jørgensen Mette1,Helleday Thomas34,Syljuåsen Randi G.2,Sørensen Claus Storgaard1

Affiliation:

1. Biotech Research and Innovation Centre, University of Copenhagen, 2200 Copenhagen N, Denmark

2. Department of Radiation Biology and Department of Tumor Biology, Institute for Cancer Research, Norwegian Radium Hospital, Oslo University Hospital, 0310 Oslo, Norway

3. Department of Genetics, Microbiology, and Toxicology, Stockholm University, S-106 91 Stockholm, Sweden

4. Gray Institute for Radiation Oncology and Biology, University of Oxford, Oxford OX3 7DQ, England, UK

Abstract

Maintenance of genome integrity is of critical importance to cells. To identify key regulators of genomic integrity, we screened a human cell line with a kinome small interfering RNA library. WEE1, a major regulator of mitotic entry, and CHK1 were among the genes identified. Both kinases are important negative regulators of CDK1 and -2. Strikingly, WEE1 depletion rapidly induced DNA damage in S phase in newly replicated DNA, which was accompanied by a marked increase in single-stranded DNA. This DNA damage is dependent on CDK1 and -2 as well as the replication proteins MCM2 and CDT1 but not CDC25A. Conversely, DNA damage after CHK1 inhibition is highly dependent on CDC25A. Furthermore, the inferior proliferation of CHK1-depleted cells is improved substantially by codepletion of CDC25A. We conclude that the mitotic kinase WEE1 and CHK1 jointly maintain balanced cellular control of Cdk activity during normal DNA replication, which is crucial to prevent the generation of harmful DNA lesions during replication.

Publisher

Rockefeller University Press

Subject

Cell Biology

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