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Article

Shelterin and subtelomeric DNA sequences control nucleosome maintenance and genome stability

Thomas S van Emden, View ORCID ProfileMarta Forn, Ignasi Forné, Zsuzsa Sarkadi, Matías Capella, Lucía Martín Caballero, Sabine Fischer‐Burkart, Cornelia Brönner, Marco Simonetta, David Toczyski, Mario Halic, View ORCID ProfileAxel Imhof, View ORCID ProfileSigurd Braun
DOI 10.15252/embr.201847181 | Published online 12.11.2018
EMBO reports (2019) 20, e47181
Thomas S van Emden
Department of Physiological Chemistry, BioMedical Center (BMC), Ludwig Maximilians University of Munich, Martinsried, GermanyInternational Max Planck Research School for Molecular and Cellular Life Sciences, Martinsried, Germany
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Marta Forn
Department of Physiological Chemistry, BioMedical Center (BMC), Ludwig Maximilians University of Munich, Martinsried, Germany
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Ignasi Forné
Protein Analysis Unit (ZfP), BioMedical Center (BMC), Ludwig Maximilians University of Munich, Martinsried, Germany
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Zsuzsa Sarkadi
Department of Physiological Chemistry, BioMedical Center (BMC), Ludwig Maximilians University of Munich, Martinsried, Germany
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Matías Capella
Department of Physiological Chemistry, BioMedical Center (BMC), Ludwig Maximilians University of Munich, Martinsried, Germany
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Lucía Martín Caballero
Department of Physiological Chemistry, BioMedical Center (BMC), Ludwig Maximilians University of Munich, Martinsried, GermanyInternational Max Planck Research School for Molecular and Cellular Life Sciences, Martinsried, Germany
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Sabine Fischer‐Burkart
Department of Physiological Chemistry, BioMedical Center (BMC), Ludwig Maximilians University of Munich, Martinsried, Germany
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Cornelia Brönner
Department of Biochemistry, Gene Center, Ludwig Maximilians University of Munich, Munich, Germany
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Marco Simonetta
Department of Biophysics and Biochemistry, University of California San Francisco (UCSF), San Francisco, CA, USA
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David Toczyski
Department of Biophysics and Biochemistry, University of California San Francisco (UCSF), San Francisco, CA, USA
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Mario Halic
Department of Biochemistry, Gene Center, Ludwig Maximilians University of Munich, Munich, Germany
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Axel Imhof
Protein Analysis Unit (ZfP), BioMedical Center (BMC), Ludwig Maximilians University of Munich, Martinsried, Germany
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Sigurd Braun
Department of Physiological Chemistry, BioMedical Center (BMC), Ludwig Maximilians University of Munich, Martinsried, GermanyInternational Max Planck Research School for Molecular and Cellular Life Sciences, Martinsried, Germany
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Author Affiliations

  1. Thomas S van Emden1,2,†,
  2. Marta Forn1,†,
  3. Ignasi Forné3,
  4. Zsuzsa Sarkadi1,
  5. Matías Capella1,
  6. Lucía Martín Caballero1,2,
  7. Sabine Fischer‐Burkart1,
  8. Cornelia Brönner4,
  9. Marco Simonetta5,6,
  10. David Toczyski5,
  11. Mario Halic4,
  12. Axel Imhof3 and
  13. Sigurd Braun (sigurd.braun{at}bmc.med.lmu.de)*,1,2
  1. 1Department of Physiological Chemistry, BioMedical Center (BMC), Ludwig Maximilians University of Munich, Martinsried, Germany
  2. 2International Max Planck Research School for Molecular and Cellular Life Sciences, Martinsried, Germany
  3. 3Protein Analysis Unit (ZfP), BioMedical Center (BMC), Ludwig Maximilians University of Munich, Martinsried, Germany
  4. 4Department of Biochemistry, Gene Center, Ludwig Maximilians University of Munich, Munich, Germany
  5. 5Department of Biophysics and Biochemistry, University of California San Francisco (UCSF), San Francisco, CA, USA
  6. 6Present Address: Department of Molecular Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands
  1. ↵*Corresponding author. Tel: +49 89 2180 77128; E‐mail: sigurd.braun{at}bmc.med.lmu.de
  1. ↵† These authors contributed equally to this work

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Abstract

Telomeres and the shelterin complex cap and protect the ends of chromosomes. Telomeres are flanked by the subtelomeric sequences that have also been implicated in telomere regulation, although their role is not well defined. Here, we show that, in Schizosaccharomyces pombe, the telomere‐associated sequences (TAS) present on most subtelomeres are hyper‐recombinogenic, have metastable nucleosomes, and unusual low levels of H3K9 methylation. Ccq1, a subunit of shelterin, protects TAS from nucleosome loss by recruiting the heterochromatic repressor complexes CLRC and SHREC, thereby linking nucleosome stability to gene silencing. Nucleosome instability at TAS is independent of telomeric repeats and can be transmitted to an intrachromosomal locus containing an ectopic TAS fragment, indicating that this is an intrinsic property of the underlying DNA sequence. When telomerase recruitment is compromised in cells lacking Ccq1, DNA sequences present in the TAS promote recombination between chromosomal ends, independent of nucleosome abundance, implying an active function of these sequences in telomere maintenance. We propose that Ccq1 and fragile subtelomeres co‐evolved to regulate telomere plasticity by controlling nucleosome occupancy and genome stability.

Synopsis

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The AT‐rich telomere‐associated sequences (TAS) in S. pombe are hyper‐recombinogenic and have metastable nucleosomes. This fragile nature of subtelomeres is counteracted by the shelterin subunit Ccq1 and its downstream partners CLRC and SHREC.

  • Ccq1 protects TAS from nucleosome loss by recruiting the heterochromatic repressor complexes CLRC and SHREC.

  • Nucleosome instability is independent of the chromosomal position and an intrinsic feature of the subtelomeric DNA sequence.

  • TAS promote recombination of chromosomal ends in the absence of Ccq1.

  • genome stability
  • heterochromatin
  • nucleosomes
  • shelterin
  • telomeres

EMBO Reports (2019) 20: e47181

  • Received October 3, 2018.
  • Revision received October 3, 2018.
  • Accepted October 12, 2018.
  • © 2018 The Authors
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Volume 20, Issue 1
01 January 2019
EMBO reports: 20 (1)
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