Volume 271, Number 31,
Issue of August 2, 1996
pp. 18485-18493
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
Condensation of Rat Telomere-specific Nucleosomal Arrays
Containing Unusually Short DNA Repeats and Histone H1
(Received for publication, March 20, 1996, and in revised form, May 16, 1996)
Jirair K.
Bedoyan
§
,
Serguei
Lejnine
§
,
Vladimir L.
Makarov
§
and
John P.
Langmore
§
From the
Graduate Program in Cellular and Molecular
Biology, § Biophysics Research Division, and
Department of Biological Sciences, The University of Michigan,
Ann Arbor, Michigan 48109-1055
Vertebrate telomeres contain arrays of
nucleosomes with unusually short and regular repeat lengths (Makarov,
V. L., Lejnine, S., Bedoyan, J., and Langmore, J. P. (1993) Cell
73, 775-787; Lejnine, S., Makarov, V., and Langmore, J. P. (1995) Proc. Natl. Acad. Sci. U. S. A. 92, 2393-2397).
In order to better define the specific structural features of telomere
chromatin, we examined the condensation and H1 content of telomere
nucleoproteins from rat liver. Velocity sedimentation analysis shows
that telomeric nucleosome arrays condense with increasing ionic
strength and molecular weight in a manner comparable with that of bulk
chromatin despite the very short repeat length. However, these
condensed structures do not exhibit the ~100-base pair
deoxyribonuclease II repeat characteristic of condensed bulk chromatin.
Frictional coefficient calculations suggest that telomere-specific
higher order structure is more compact than bulk chromatin.
Nucleoprotein gel electrophoresis shows that telomeric dinucleosomes
from soluble chromatin contain H1. Finally, direct isolation and
analysis of telomere nucleoproteins from formaldehyde-cross-linked
nuclei indicate the presence of core histone proteins and H1. These
results are consistent with the view that a major fraction of the long
telomeres of rat are organized as specialized nucleosome arrays with
features similar but not identical to those of bulk chromatin.