TRF2-Mediated Control of Telomere DNA Topology as a Mechanism for Chromosome-End Protection

Mol Cell. 2016 Jan 21;61(2):274-86. doi: 10.1016/j.molcel.2015.12.009. Epub 2016 Jan 7.

Abstract

The shelterin proteins protect telomeres against activation of the DNA damage checkpoints and recombinational repair. We show here that a dimer of the shelterin subunit TRF2 wraps ∼ 90 bp of DNA through several lysine and arginine residues localized around its homodimerization domain. The expression of a wrapping-deficient TRF2 mutant, named Top-less, alters telomeric DNA topology, decreases the number of terminal loops (t-loops), and triggers the ATM checkpoint, while still protecting telomeres against non-homologous end joining (NHEJ). In Top-less cells, the protection against NHEJ is alleviated if the expression of the TRF2-interacting protein RAP1 is reduced. We conclude that a distinctive topological state of telomeric DNA, controlled by the TRF2-dependent DNA wrapping and linked to t-loop formation, inhibits both ATM activation and NHEJ. The presence of RAP1 at telomeres appears as a backup mechanism to prevent NHEJ when topology-mediated telomere protection is impaired.

Keywords: DNA topology; DNA wrapping; RAP1; TRF2; telomere.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Ataxia Telangiectasia Mutated Proteins / metabolism
  • Base Pairing
  • DNA / chemistry*
  • DNA / metabolism
  • DNA Damage
  • DNA End-Joining Repair
  • HeLa Cells
  • Humans
  • Lysine / metabolism
  • Models, Molecular
  • Mutation
  • Nucleic Acid Conformation*
  • Protein Structure, Tertiary
  • Shelterin Complex
  • Signal Transduction
  • Telomere / metabolism*
  • Telomere-Binding Proteins / metabolism
  • Telomeric Repeat Binding Protein 2 / chemistry
  • Telomeric Repeat Binding Protein 2 / metabolism*

Substances

  • Shelterin Complex
  • TERF2IP protein, human
  • Telomere-Binding Proteins
  • Telomeric Repeat Binding Protein 2
  • DNA
  • Ataxia Telangiectasia Mutated Proteins
  • Lysine