Nucleic Acids Research, Vol 24, Issue 8 1412-1419, Copyright © 1996 by Oxford University Press
M Duffy and A Chambers
Gel retardation assays using a probe containing the repeat region of a
Schizosaccharomyces pombe chromosomal telomere identified four specific
DNA- protein complexes in S. pombe total protein extracts (I, I', IIa and
IIb). The proteins responsible for these complexes bound to the telomeric
repeat region irrespective of whether or not the repeats were in close
proximity to the end of a DNA molecule, and none of them bound strongly to
single-stranded DNA. The protein responsible for complex I (TeRF I) was
separated from the activity responsible for complexes IIa and IIb (TeRF II)
using heparin-Sepharose chromatography. Both factors were efficiently
cross-competed by an oligonucleotide containing the 18 bp sequence
5'-GGTTACAGGTTACAGGTT-3', which corresponds to two complete telomeric
repeat units. Mutation of the T residues at positions 4 and 11 in the
oligonucleotide dramatically reduced binding by TeRF II, but had no affect
on binding by TeRF I. The protein responsible for complex I' did not bind
strongly to either the wild-type or mutant oligonucleotide.
ARTICLES
DNA-protein interactions at the telomeric repeats of Schizosaccharomyces pombe
Department of Genetics, University of Nottingham, Queen's Medical Centre, UK.
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