Functional complementation of the radiation-sensitive mutant M10 cell line by human chromosome 5

Mutat Res. 1994 Jan-Feb;323(1-2):47-52. doi: 10.1016/0165-7992(94)90044-2.

Abstract

The mouse lymphoma (L5178Y) cell mutant M10 is defective in rejoining DNA double-strand breaks and is hypersensitive to ionizing radiation. The introduction of human chromosome 5 into M10 cells by microcell mediated chromosome transfer complemented the ionizing-radiation hypersensitivity defect of this cell line. The presence of chromosome 5 in the microcell hybrids was shown using PCR with chromosome-specific primers and fluorescence in situ hybridization. From this data we conclude that the gene that corrects the radiation hypersensitivity of M10 cells is located on chromosome 5 and tentatively assigned to the 5q14 to 5pter region. We designate this gene XRCC4L.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Chromosomes, Human, Pair 5*
  • DNA Repair / genetics
  • Genetic Complementation Test*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Mice
  • Mutation*
  • Polymerase Chain Reaction
  • Radiation Tolerance
  • Tumor Cells, Cultured