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DNA repair in Escherichia coli: the dual function of uvr genes.

Abstract
It has been shown earlier that the starvation of E. coli for both amino-acids and thymine applied prior to UV irradiation inhibits pyrimidine dimer excision without affecting cell survival after UV irradiation. In such cells pyrimidine dimers are tolerated by a rather error-free process that depends on the activity of uvrB, recA and lexA genes. Data presented here show: (a) that the efficient toleration of unexcised dimers requires also the uvrA gene; (b) that the starvation increases the level of RecA protein about 4.7 times; (c) that the effect of starvation on subsequent pyrimidine dimer excision is reversed by a 2 h incubation in complete medium before the cells are UV irradiated. The data suggest that the uvrA, uvrB, recA, lexA dependent nonexcisional repair may be a pathway temporarily functioning in repeatedly damaged cells.
AuthorsF Masek, I Fridrichova, M Pirsel, M Sedliaková
JournalNeoplasma (Neoplasma) Vol. 42 Issue 6 Pg. 317-23 ( 1995) ISSN: 0028-2685 [Print] Slovakia
PMID8592574 (Publication Type: Journal Article)
Chemical References
  • Bacterial Proteins
  • DNA, Bacterial
  • DNA-Binding Proteins
  • Escherichia coli Proteins
  • UvrB protein, E coli
  • Rec A Recombinases
  • UvrA protein, E coli
  • Adenosine Triphosphatases
  • DNA Helicases
Topics
  • Adenosine Triphosphatases (genetics)
  • Bacterial Proteins (genetics)
  • DNA Helicases
  • DNA Repair
  • DNA, Bacterial (biosynthesis)
  • DNA-Binding Proteins (genetics)
  • Escherichia coli (genetics)
  • Escherichia coli Proteins
  • Genes, Bacterial
  • Rec A Recombinases (analysis)

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