4.8 Article

The effect of the TRF2 N-terminal and TRFH regions on telomeric G-quadruplex structures

Journal

NUCLEIC ACIDS RESEARCH
Volume 37, Issue 5, Pages 1541-1554

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkn1081

Keywords

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Funding

  1. James and Esther King, Florida Biomedical Research Program [04NAR-06]
  2. American Heart Association [07552813]

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The sequence of human telomeric DNA consists of tandem repeats of 5-d(TTAGGG)-3. This guanine-rich DNA can form G-quadruplex secondary structures which may affect telomere maintenance. A current model for telomere protection by the telomere-binding protein, TRF2, involves the formation of a t-loop which is stabilized by a strand invasion-like reaction. This type of reaction may be affected by G-quadruplex structures. We analyzed the influence of the arginine-rich, TRF2 N-terminus (TRF2(B)), as well as this region plus the TRFH domain of TRF2 (TRF2(BH)), on the structure of G-quadruplexes. Circular dichroism results suggest that oligonucleotides with 4, 7 and 8 5-d(TTAGGG)-3 repeats form hybrid structures, a mix of parallel/antiparallel strand orientation, in K. TRF2(B) stimulated the formation of parallel-stranded structures and, in some cases, intermolecular structures. TRF2(BH) also stimulated intermolecular but not parallel-stranded structures. Only full-length TRF2 and TRF2(BH) stimulated uptake of a telomeric single-stranded oligonucleotide into a plasmid containing telomeric DNA in the presence of K. The results in this study suggest that G-quadruplex formation inhibits oligonucleotide uptake into the plasmid, but the inhibition can be overcome by TRF2. This study is the first analysis of the effects of TRF2 domains on G-quadruplex structures and has implications for the role of G-quadruplexes and TRF2 in the formation of t-loops.

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