Accumulation of DSBs in gamma-H2AX domains fuel chromosomal aberrations

Biochem Biophys Res Commun. 2008 Jul 11;371(4):694-7. doi: 10.1016/j.bbrc.2008.04.127. Epub 2008 May 5.

Abstract

DNA double strand breaks (DSBs) pose a severe hazard to the genome as erroneous rejoining of DSBs can lead to mutation and cancer. Here, we have investigated the correlation between X irradiation-induced gamma-H2AX foci, theoretically induced DSBs, and the minimal number of mis-rejoined DNA breaks (MNB) in irradiated lymphocytes obtained from two healthy humans by painting of the whole chromosome complement by spectral karyotyping. There were less gamma-H2AX foci/dose than theoretically expected, while misrepair, as expressed by MNB/gamma-H2AX focus, was similar at 0.5 and 1Gy but 3.6-fold up at 3Gy. Hence, our results suggest that X-ray-induced gamma-H2AX foci in G0 lymphocyte nuclei contain more than one DSB and that the increasing number of DSBs per gamma-H2AX repair factory lead to an increased rate of misrepair.

MeSH terms

  • Cell Nucleus / metabolism
  • Cell Nucleus / radiation effects
  • Chromosome Breakage*
  • DNA Breaks, Double-Stranded*
  • DNA Repair*
  • Histones / analysis
  • Histones / metabolism*
  • Histones / radiation effects*
  • Humans
  • Karyotyping
  • Lymphocytes / radiation effects
  • Lymphocytes / ultrastructure
  • Protein Structure, Tertiary
  • Resting Phase, Cell Cycle
  • X-Rays

Substances

  • H2AX protein, human
  • Histones