Nucleic Acids Research, Vol 26, Issue 13 3146-3153, Copyright © 1998 by Oxford University Press
A Errami, DM He, AA Friedl, WJ Overkamp, B Morolli, EA Hendrickson, F Eckardt- Schupp, M Oshimura, PH Lohman, SP Jackson and MZ Zdzienicka
DNA-dependent protein kinase (DNA-PK) plays an important role in DNA
double-strand break (DSB) repair and V(D)J recombination. We have isolated
a new X-ray-sensitive CHO cell line, XR-C1, which is impaired in DSB repair
and which was assigned to complementation group 7, the group that is
defective in the XRCC7 / SCID ( Prkdc ) gene encoding the catalytic subunit
of DNA-PK (DNA-PKcs). Consistent with this complementation analysis, XR-C1
cells lackeddetectable DNA-PKcs protein, did not display DNA-PK catalytic
activity and were complemented by the introduction of a single human
chromosome 8 (providing the Prkdc gene). The impact of the XR-C1 mutation
on V(D)J recombination was quite different from that found in most rodent
cells defective in DNA-PKcs, which are preferentially blocked in coding
joint formation, whereas XR-C1 cells were defective in forming both coding
and signal joints. These results suggest that DNA-PKcs is required for both
coding and signal joint formation during V(D)J recombination and that the
XR-C1 mutant cell line may prove to be a useful tool in understanding this
pathway.
ARTICLES
XR-C1, a new CHO cell mutant which is defective in DNA-PKcs, is impaired in both V(D)J coding and signal joint formation
Department of Radiation Genetics and Chemical Mutagenesis, MGC, Leiden University-Medical Center, Leiden, The Netherlands.
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