Characterization of gamma irradiation-induced mutations in Arabidopsis mutants deficient in non-homologous end joining

J Radiat Res. 2020 Sep 8;61(5):639-647. doi: 10.1093/jrr/rraa059.

Abstract

To investigate the involvement of the non-homologous end joining (NHEJ) pathway in plant mutagenesis by ionizing radiation, we conducted a genome-wide characterization of the mutations induced by gamma rays in NHEJ-deficient Arabidopsis mutants (AtKu70-/- and AtLig4-/-). Although both mutants were more sensitive to gamma rays than the wild-type control, the AtKu70-/- mutant was slightly more sensitive than the AtLig4-/- mutant. Single-base substitutions (SBSs) were the predominant mutations in the wild-type control, whereas deletions (≥2 bp) and complex-type mutations [i.e. more than two SBSs or short insertion and deletions (InDels) separated by fewer than 10 bp] were frequently induced in the mutants. Single-base deletions were the most frequent deletions in the wild-type control, whereas the most common deletions in the mutants were 11-30 bp. The apparent microhomology at the rejoined sites of deletions peaked at 2 bp in the wild-type control, but was 3-4 bp in the mutants. This suggests the involvement of alternative end joining and single-strand annealing pathways involving increased microhomology for rejoining DNA ends. Complex-type mutations comprising short InDels were frequently detected in the mutants, but not in the wild-type control. Accordingly, NHEJ is more precise than the backup pathways, and is the main pathway for rejoining the broken DNA ends induced by ionizing radiation in plants.

Keywords: Ku70; Lig4; Arabidopsis; NHEJ; gamma ray; mutation.

MeSH terms

  • Arabidopsis / genetics*
  • Arabidopsis / radiation effects*
  • Base Pairing / genetics
  • DNA End-Joining Repair / genetics*
  • DNA End-Joining Repair / radiation effects*
  • Gamma Rays*
  • Gene Expression Regulation, Plant
  • Genes, Plant
  • INDEL Mutation / genetics
  • Mutation / genetics*
  • Mutation Rate
  • Seeds / radiation effects
  • Sequence Deletion / genetics
  • Transcription, Genetic