RAD9, RAD24, RAD16 and RAD26 are required for the inducible nucleotide excision repair of UV-induced cyclobutane pyrimidine dimers from the transcribed and non-transcribed regions of the Saccharomyces cerevisiae MFA2 gene

Mutat Res. 2001 Apr 4;485(3):229-36. doi: 10.1016/s0921-8777(01)00061-1.

Abstract

In this study, the effect of a prior UV irradiation on the removal of cyclobutane pyrimidine dimers (CPDs) from the transcribed strand (TS) and non-transcribed strand (NTS) of the MFA2 gene in haploid Saccharomyces cerevisiae (S. cerevisiae) cells was investigated. In NER competent cells, the pre-irradiation with a dose of 20J/m2 enhances the removal of CPDs induced by a second UV dose of 100J/m2 in the TS and the NTS of MFA2 gene except for the CPDs in the region +258 to +298 in the NTS, where the enhanced repair was absent. No inducible repair was observed in rad9, rad24, rad16 and rad26 cells, indicating two checkpoint genes RAD9 and RAD24, the global repair gene RAD16 and the transcription coupled repair gene RAD26 are essential for inducible NER.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • DNA Repair*
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism
  • Genes, Fungal / radiation effects*
  • Mutation
  • Pyrimidine Dimers / metabolism*
  • Saccharomyces cerevisiae / genetics*
  • Ultraviolet Rays / adverse effects

Substances

  • Cell Cycle Proteins
  • Fungal Proteins
  • Pyrimidine Dimers