Mammalian Ku86 mediates chromosomal fusions and apoptosis caused by critically short telomeres

EMBO J. 2002 May 1;21(9):2207-19. doi: 10.1093/emboj/21.9.2207.

Abstract

Here we analyze the functional interaction between Ku86 and telomerase at the mammalian telomere by studying mice deficient for both proteins. We show that absence of Ku86 prevents the end-to-end chromosomal fusions that result from critical telomere shortening in telomerase-deficient mice. In addition, Ku86 deficiency rescues the male early germ cell apoptosis triggered by short telomeres in these mice. Together, these findings define a role for Ku86 in mediating chromosomal instability and apoptosis triggered by short telomeres. In addition, we show here that Ku86 deficiency results in telomerase-dependent telomere elongation and in the fusion of random pairs of chromosomes in telomerase-proficient cells, suggesting a model in which Ku86 keeps normal-length telomeres less accessible to telomerase-mediated telomere lengthening and to DNA repair activities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Nuclear*
  • Apoptosis / physiology*
  • Chromosome Aberrations*
  • Chromosomes / metabolism
  • DNA Helicases*
  • DNA-Binding Proteins / deficiency
  • DNA-Binding Proteins / metabolism
  • DNA-Binding Proteins / physiology*
  • Ku Autoantigen
  • Male
  • Mice
  • Mice, Knockout
  • Nuclear Proteins / deficiency
  • Nuclear Proteins / physiology*
  • Spermatozoa / physiology
  • Telomerase / deficiency
  • Telomerase / physiology*
  • Telomere / metabolism
  • Telomere / physiology*

Substances

  • Antigens, Nuclear
  • DNA-Binding Proteins
  • Nuclear Proteins
  • Telomerase
  • DNA Helicases
  • XRCC5 protein, human
  • Xrcc5 protein, mouse
  • Xrcc6 protein, human
  • Xrcc6 protein, mouse
  • Ku Autoantigen