Transcription-coupled repair deficiency and mutations in human mismatch repair genes

Science. 1996 Apr 26;272(5261):557-60. doi: 10.1126/science.272.5261.557.

Abstract

Deficiencies in mismatch repair have been linked to a common cancer predisposition syndrome in humans, hereditary nonpolyposis colorectal cancer (HNPCC), and a subset of sporadic cancers. Here, several mismatch repair-deficient tumor cell lines and HNPCC-derived lymphoblastoid cell lines were found to be deficient in an additional DNA repair process termed transcription-coupled repair (TCR). The TCR defect was corrected in a mutant cell line whose mismatch repair deficiency had been corrected by chromosome transfer. Thus, the connection between excision repair and mismatch repair previously described in Escherichia coli extends to humans. These results imply that deficiencies in TCR and exposure to carcinogens present in the environment may contribute to the etiology of tumors associated with genetic defects in mismatch repair.

Publication types

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

MeSH terms

  • Adenosine Triphosphatases*
  • Colorectal Neoplasms, Hereditary Nonpolyposis / genetics*
  • DNA Damage
  • DNA Repair Enzymes*
  • DNA Repair*
  • DNA-Binding Proteins*
  • Humans
  • Lymphocytes / cytology
  • Mismatch Repair Endonuclease PMS2
  • MutS Homolog 2 Protein
  • Mutation*
  • Neoplasm Proteins / genetics
  • Neoplasms / genetics*
  • Proto-Oncogene Proteins / genetics
  • Pyrimidine Dimers / metabolism
  • Tetrahydrofolate Dehydrogenase / genetics
  • Transcription, Genetic*
  • Tumor Cells, Cultured
  • Ultraviolet Rays

Substances

  • DNA-Binding Proteins
  • Neoplasm Proteins
  • Proto-Oncogene Proteins
  • Pyrimidine Dimers
  • Tetrahydrofolate Dehydrogenase
  • Adenosine Triphosphatases
  • PMS2 protein, human
  • MSH2 protein, human
  • Mismatch Repair Endonuclease PMS2
  • MutS Homolog 2 Protein
  • DNA Repair Enzymes