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Human Molecular Genetics Advance Access published online on November 25, 2003

Human Molecular Genetics, doi:10.1093/hmg/ddh022
© 2003 by Oxford University Press
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©2003 Oxford University Press

Article

A tumour derived mutant allele of XRCC2 preferentially suppresses homologous recombination at DNA replication forks

Atul Mohindra 1, Emma Bolderson 1, Jason Stone 2, Michael Wells 3, Thomas Helleday 1, and Mark Meuth 4*

1 Institute for Cancer Studies, University of Sheffield, School of Medicine, Sheffield, S10 2RX, UK
2 Department of Histopathology, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Trust, Sheffield, S10 2UL, UK
3 Academic Unit of Pathology, University of Sheffield, School of Medicine, Sheffield S10 2RX, UK
4 Institute for Cancer Studies, The University of Sheffield School of Medicine, Beech Hill Road, Sheffield, S10 2RX, UK

* To whom correspondence should be addressed. E-mail: m.meuth{at}sheffield.ac.uk.


   Abstract

Homologous recombination repair (HRR) is required for both the repair of DNA double strand breaks (DSBs) and the maintenance of the integrity of DNA replication forks. To determine the effect of a mutant allele of the RAD51 paralog XRCC2 (342delT) found in a HRR defective tumour cell line, we introduced 342delT into HRR proficient cells containing a recombination reporter substrate. In one set of transfectants, expression of 342delT conferred sensitivity to thymidine and mitomycin C and suppressed HRR induced at the recombination reporter by thymidine but not by DSBs. In a second set of transfectants, the expression of 342delT was accompanied by a decreased level of the full length XRCC2. These cells were defective in the induction of HRR by either thymidine or DSBs. Thus 342delT suppresses recombination induced by thymidine in a dominant negative manner while recombination induced by DSBs appears to depend upon the level of XRCC2 as well as the expression of the mutant XRCC2 allele. These results suggest that HRR pathways responding to stalled replication forks or DSBs are genetically distinguishable. They further suggest a critical role for XRCC2 in HRR at replication forks, possibly in the loading of RAD51 onto gapped DNA.


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