Streamlining effects of extra telomeric repeat on telomeric DNA folding revealed by fluorescence-force spectroscopy
Author(s) -
Jaba Mitra,
Taekjip Ha
Publication year - 2019
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkz906
Subject(s) - biology , folding (dsp implementation) , dna , telomere , fluorescence , biophysics , force spectroscopy , genetics , computational biology , atomic force microscopy , evolutionary biology , nanotechnology , physics , quantum mechanics , electrical engineering , engineering , materials science
A human telomere ends in a single-stranded 3' tail, composed of repeats of T2AG3. G-quadruplexes (GQs) formed from four consecutive repeats have been shown to possess high-structural and mechanical diversity. In principle, a GQ can form from any four repeats that are not necessarily consecutive. To understand the dynamics of GQs with positional multiplicity, we studied five and six repeats human telomeric sequence using a combination of single molecule FRET and optical tweezers. Our results suggest preferential formation of GQs at the 3' end both in K+ and Na+ solutions, with minor populations of 5'-GQ or long-loop GQs. A vectorial folding assay which mimics the directional nature of telomere extension showed that the 3' preference holds even when folding is allowed to begin from the 5' side. In 100 mM K+, the unassociated T2AG3 segment has a streamlining effect in that one or two mechanically distinct species was observed at a single position instead of six or more observed without an unassociated repeat. We did not observe such streamlining effect in 100 mM Na+. Location of GQ and reduction in conformational diversity in the presence of extra repeats have implications in telomerase inhibition, T-loop formation and telomere end protection.
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