Persistence of DNA threads in human anaphase cells suggests late completion of sister chromatid decatenation

Chromosoma. 2008 Apr;117(2):123-35. doi: 10.1007/s00412-007-0131-7. Epub 2007 Nov 8.

Abstract

PICH (Plk1-interacting checkpoint helicase) was recently identified as an essential component of the spindle assembly checkpoint and shown to localize to kinetochores, inner centromeres, and thin threads connecting separating chromosomes even during anaphase. In this paper, we have used immuno-fiber fluorescence in situ hybridization and chromatin-immunoprecipitation to demonstrate that PICH associates with centromeric chromatin during anaphase. Furthermore, by careful analysis of PICH-positive anaphase threads through FISH as well as bromo-deoxyurdine and CREST labeling, we strengthen the evidence that these threads comprise mainly alphoid centromere deoxyribonucleic acid. Finally, by timing the addition of ICRF-193 (a specific inhibitor of topoisomerase-II alpha) to cells synchronized in anaphase, we demonstrate that topoisomerase activity is required specifically to resolve PICH-positive threads during anaphase (as opposed to being required to prevent the formation of such threads during earlier cell cycle stages). These data indicate that PICH associates with centromeres during anaphase and that most PICH-positive threads evolve from inner centromeres as these stretch in response to tension. Moreover, they show that topoisomerase activity is required during anaphase for the resolution of PICH-positive threads, implying that the complete separation of sister chromatids occurs later than previously assumed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anaphase*
  • Centromere / ultrastructure
  • Centrosome / ultrastructure
  • Chromatids / ultrastructure*
  • Chromatin / metabolism
  • Chromosome Segregation*
  • DNA Helicases / genetics*
  • DNA Topoisomerases, Type II / metabolism
  • HeLa Cells
  • Humans
  • Image Processing, Computer-Assisted
  • In Situ Hybridization, Fluorescence
  • Kinetochores
  • Microscopy, Fluorescence
  • Nucleic Acid Hybridization

Substances

  • Chromatin
  • DNA Helicases
  • ERCC6L protein, human
  • DNA Topoisomerases, Type II