Assignment of the XRCC2 human DNA repair gene to chromosome 7q36 by complementation analysis

Nigel J. Jones, Ying Zhao, Michael J. Siciliano, Larry H. Thompson

Research output: Contribution to journalArticlepeer-review

26 Scopus citations


The V79 hamster cell line irs1 is a repair-deficient mutant hypersensitive to radiation and DNA-reactive chemical agents. Somatic cell hybrids were formed by fusing irs1 cells with human lymphocytes and selecting for complementation in medium containing concentrations of mitomycin C (MMC) that are toxic to irs1. Thirty-eight MMC-resistant hybrids showed extensive segregation of human chromosomes, with 35 of them retaining human chromosome 7, as indicated by molecular marker and cytogenetic analyses. Inter-Alu-PCR products from the DNA of hybrids, when used as fluorescence in situ hybridization probe onto normal human metaphases, indicated that one resistant hybrid was monochromosomal for chromosome 7 and that the three resistant hybrids shown to be negative for chromosome 7 markers have retained portions of chromosome 7, with region 7q36 being the smallest common region. MMC-sensitive subclones of a resistant hybrid lost human chromosome 7. Therefore, the gene complementing the repair defect, XRCC2 (X-ray repair cross complementing), is assigned to human chromosome 7q36.

Original languageEnglish (US)
Pages (from-to)619-622
Number of pages4
Issue number3
StatePublished - Apr 10 1995
Externally publishedYes

ASJC Scopus subject areas

  • Genetics


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