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Vol. 95, Issue 7, 3396-3401, March 31, 1998
* Department of Biochemistry and Biophysics, Oregon State
University, Corvallis, OR 97331-7305; and Contributed by Kensal van Holde, January 20, 1998
The protection against micrococcal nuclease digestion afforded to
chromatosomal DNA by the presence of a linker histone (H1o)
has been quantitatively measured in two reconstituted systems. We have
used chromatosomes reconstituted at two distinct positions on a DNA
fragment containing the 5S rRNA gene from Lytechinus variegatus and at a specific position on a sequence containing Gal4- and USF-binding sites. In all cases, we find asymmetric protection, with
Copyright © 1998 by The National Academy of Sciences 0027-8424/98/953396-6$2.00/0
Biochemistry
Linker histone protects linker DNA on only one side of the core
particle and in a sequence-dependent manner
,
Institute of
Genetics, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria
20 bp protected on one side of the core particle and no protection on the other. We demonstrated through crosslinking experiments that the result is not due to any sliding of the histone core caused by either linker histone addition or micrococcal nuclease cleavage. Because the core particle is itself a symmetric object, the
preferred asymmetric location of a linker histone must be dictated by
unknown elements in the DNA sequence.
Present address: Department of Physics and Astronomy,
Arizona State University, P.O. Box 871504, Tempe, AZ 85287-1504.
§
To whom reprint requests should be addressed at: Department
of Biochemistry and Biophysics, Oregon State University, Corvallis, OR
97331-7305. e-mail: zlatanoj{at}ucs.orst.edu.
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