Nucleic Acids Research, Vol 26, Issue 13 3084-3089, Copyright © 1998 by Oxford University Press
R Cartwright, CE Tambini, PJ Simpson and J Thacker
We recently identified a positional candidate for the XRCC2 DNA repair gene
at human chromosome 7q36.1. We have now cloned the cDNA for this gene from
both human and mouse and show that it is a highly conserved novel member of
the recA / RAD51 recombination repair gene family. The cDNA is able to
complement significantly the phenotype of a unique cell line, irs1 , which
shows extreme sensitivity to DNA cross-linking agents and genetic
instability. Thisphenotype is consistent with a role for the XRCC2 gene in
recombination repair in somatic cells, suggesting that in addition to RAD51
, other members of this gene family have an important function in high
fidelity repair processes in mammals. Despite this function, the XRCC2 gene
transcript is expressed at a very low level in somatic tissue, but is
elevated in mouse testis, suggesting an additional role in meiosis.
ARTICLES
The XRCC2 DNA repair gene from human and mouse encodes a novel member of the recA/RAD51 family
Medical Research Council, Radiation and Genome Stability Unit, Harwell, Oxfordshire OX11 0RD, UK.
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