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Chapter 10. Multiple Pathways Tether Telomeres and Silent Chromatin at the Nuclear Periphery: Functional Implications for Sir-Mediated Repression

  1. Derek J. Chadwick Organizer,
  2. Jamie Goode
  1. Angela Taddei,
  2. Marc R. Gartenberg,
  3. Frank R. Neumann,
  4. Florence Hediger,
  5. Susan M. Gasser

Published Online: 7 OCT 2008

DOI: 10.1002/0470093765.ch10

Nuclear Organization in Development and Disease: Novartis Foundation Symposium 264

Nuclear Organization in Development and Disease: Novartis Foundation Symposium 264

How to Cite

Taddei, A., Gartenberg, M. R., Neumann, F. R., Hediger, F. and Gasser, S. M. (2008) Multiple Pathways Tether Telomeres and Silent Chromatin at the Nuclear Periphery: Functional Implications for Sir-Mediated Repression, in Nuclear Organization in Development and Disease: Novartis Foundation Symposium 264 (eds D. J. Chadwick and J. Goode), John Wiley & Sons, Ltd, Chichester, UK. doi: 10.1002/0470093765.ch10

Author Information

  1. University of Geneva, Department of Molecular Biology and NCCR Frontiers in Genetics, Quai, Ernest-Ansermet 30, CH-1211 Geneva 4, Switzerland

  1. Friedrich Miescher Institute for Biomedical Research, Marlbeerstrasse 66, CH-4058 Basel, Switzerland

Publication History

  1. Published Online: 7 OCT 2008
  2. Published Print: 14 JAN 2005

Book Series:

  1. Novartis Foundation Symposia

Book Series Editors:

  1. Novartis Foundation

ISBN Information

Print ISBN: 9780470093733

Online ISBN: 9780470093764

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Keywords:

  • LexA-fusion targeting;
  • GFP-tagged chromosomal domains;
  • inducible site-specific recombination;
  • HMR silent mating-type locus;
  • dual anchoring pathways;
  • chromatin mobility;
  • Sir-dependent pathway;
  • perinuclear anchoring in repression;
  • clustering-feedback loop

Summary

The positioning of chromosomal domains within interphase nuclei is thought to contribute to establishment and maintenance of epigenetic control. Using GFP-tagged chromosomal domains, LexA-fusion targeting and live microscopy, we investigated mechanisms through which chromatin can be anchored to the nuclear envelope (NE). We find that a subdomain of the silencing information regulator Sir4 (Sir4PAD) and yKu80 are sucient to tether a chromatin region to the nuclear periphery, independently of their silencing function. Sir4PAD interacts with Esc1 (Establishes Silent Chromatin 1), a large acidic protein, localized at the nuclear periphery in the absence of Sir4 and yKu. Sir4 also binds to the periphery through yKu80, whose perinuclear ligand is unidentified. Both pathways are involved in the localization of natural telomeres. To show that silent chromatin can also mediate anchorage, we uncoupled the HMR silent mating-type locus from the chromosome using inducible site-specific recombination. Real-time cytological techniques reveal the position and dynamics of the excised locus. We show that the silent HMR ring associates with the NE in a SIR-dependent manner, while derepressed excised rings move without detectable constraint throughout the nucleoplasm. Dual anchoring pathways thus cooperate to generate high concentrations of SIR proteins in perinuclear foci, which in turn promote repression.