Telomere sister chromatid exchange and the process of aging

Aging (Albany NY). 2010 Oct;2(10):727-30. doi: 10.18632/aging.100206.

Abstract

Telomeres are a hotspot for sister chromatid exchange (T-SCE). Any biological consequence of this form of instability remained obscure until quantitative modeling revealed a link between elevated T-SCE rates and accelerated cellular replicative senescence. This work strongly suggests that progressive telomere erosion is not the only determinant of replicative capacity; instead, T-SCE need to be considered as an independent factor controlling colony growth and senescence. Additionally high T-SCE rates have been observed in cells with deficiencies in WRN and BLM, the genes that are defective in Werner's and Bloom's syndromes, implying a connection to premature aging. In this Research Perspective we will explore some of the implications this recent work has for human health.

MeSH terms

  • Aging / genetics
  • Animals
  • Antioxidants / pharmacology
  • Bloom Syndrome / genetics
  • Cell Proliferation*
  • Cellular Senescence / physiology*
  • Computer Simulation
  • Exodeoxyribonucleases / genetics
  • Humans
  • Models, Biological
  • Neoplasms / genetics
  • RecQ Helicases / genetics
  • Sister Chromatid Exchange / drug effects
  • Sister Chromatid Exchange / physiology*
  • Sister Chromatid Exchange / radiation effects
  • Skin Aging / genetics
  • Skin Aging / radiation effects
  • Telomere / genetics
  • Telomere / metabolism*
  • Werner Syndrome / genetics
  • Werner Syndrome Helicase

Substances

  • Antioxidants
  • Exodeoxyribonucleases
  • Bloom syndrome protein
  • RecQ Helicases
  • WRN protein, human
  • Werner Syndrome Helicase