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Mice with DNA repair gene (ERCC-1) deficiency have elevated levels of p53, liver nuclear abnormalities and die before weaning.

Defects in nucleotide excision repair are associated with the human condition xeroderma pigmentosum which predisposes to skin cancer. Mice with defective DNA repair were generated by targeting the excision repair cross complementing gene (ERCC-1) in the embryonic stem cell line, HM-1. Homozygous ERCC-1 mutants were runted at birth and died before weaning with liver failure. Examination of organs revealed polyploidy in perinatal liver, progressing to severe aneuploidy by 3 weeks of age. Elevated p53 levels were detected in liver, brain and kidney, supporting the hypothesised role for p53 as a monitor of DNA damage.

Pubmed ID: 8275084

Authors

  • McWhir J
  • Selfridge J
  • Harrison DJ
  • Squires S
  • Melton DW

Journal

Nature genetics

Publication Data

November 4, 1993

Associated Grants

None

Mesh Terms

  • Animals
  • Base Sequence
  • Brain
  • Cell Nucleus
  • Cells, Cultured
  • DNA Damage
  • DNA Primers
  • DNA Repair
  • DNA-Binding Proteins
  • Endonucleases
  • Homozygote
  • Kidney
  • Liver
  • Liver Failure
  • Mice
  • Mice, Inbred BALB C
  • Molecular Sequence Data
  • Proteins
  • Tumor Suppressor Protein p53