| Literature DB >> 8548796 |
Z Li1, T Otevrel, Y Gao, H L Cheng, B Seed, T D Stamato, G E Taccioli, F W Alt.
Abstract
The XR-1 Chinese hamster ovary cell line is impaired in DNA double-strand break repair (DSBR) and in ability to support V(D)J recombination of transiently introduced substrates. We now show that XR-1 cells support recombination-activating gene 1- and 2-mediated initiation of V(D)J recombination within a chromosomally integrated substrate, but are highly impaired in ability to complete the process by forming coding and recognition sequence joins. On this basis, we isolated a human cDNA sequence, termed XRCC4, whose expression confers normal V(D)J recombination ability and significant restoration of DSBR activity to XR-1, clearly demonstrating that this gene product is involved in both processes. The XRCC4 gene maps to the previously identified locus on human chromosome 5, is deleted in XR-1 cells, and encodes a ubiquitously expressed product unrelated to any described protein.Entities:
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Year: 1995 PMID: 8548796 DOI: 10.1016/0092-8674(95)90135-3
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582