Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome complementation group A

Mutat Res. 1996 Feb 15;362(2):167-74. doi: 10.1016/0921-8777(95)00046-1.

Abstract

US31 is a UV-sensitive mutant cell line (rodent complementation group 8) derived from a mouse T cell line L5178Y. We analyzed removal kinetics for UV-induced cyclobutane pyrimidine dimers and (6-4) photoproducts in US31 cells using monoclonal antibodies against these photoproducts. While nearly all (6-4) photoproducts were repaired within 6 h after UV-irradiation, more than 70% of cyclobutane pyrimidine dimers remained unrepaired even 24 h after UV-irradiation. These kinetics resembled those of Cockayne syndrome (CS) cells. Since US31 cells had a low efficiency of cell fusion and transfection, which hampered both complementation tests and gene cloning, we constructed fibroblastic complementation group 8 cell line 6L1030 by fusion of US31 cells with X-irradiated normal mouse fibroblastic LTA cells. Complementation tests by cell fusion and transfection using 6L1030 cells revealed that rodent complementation group 8 corresponded to CS complementation group A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Fusion
  • Cell Line
  • Cockayne Syndrome / genetics*
  • DNA / radiation effects
  • DNA Damage
  • DNA Repair / genetics
  • DNA Repair / physiology*
  • DNA Repair Enzymes
  • DNA-Binding Proteins
  • Genetic Complementation Test / methods
  • Humans
  • Hybrid Cells
  • L Cells
  • Leukemia L5178
  • Mice
  • Proteins / genetics
  • Proteins / metabolism
  • Pyrimidine Dimers / metabolism
  • Transcription Factors
  • Transfection
  • Ultraviolet Rays*
  • Xeroderma Pigmentosum / genetics

Substances

  • Ckn1 protein, mouse
  • DNA-Binding Proteins
  • ERCC8 protein, human
  • Proteins
  • Pyrimidine Dimers
  • Transcription Factors
  • pyrimidine-pyrimidone dimer
  • DNA
  • DNA Repair Enzymes