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Molecular and Cellular Biology, March 1999, p. 2088-2097, Vol. 19, No. 3
Department of Molecular Biology,
Massachusetts General Hospital, Boston, Massachusetts
021141; Department of Genetics, Harvard
Medical School, Boston, Massachusetts 021152;
and Graduate Program, Department of Chemistry and
Biochemistry, University of Notre Dame, Notre Dame, Indiana
465563
Received 19 August 1998/Returned for modification 8 October
1998/Accepted 13 December 1998
The histone N-terminal tails have been shown previously to be
important for chromatin assembly, remodeling, and stability. We have
tested the ability of human SWI-SNF (hSWI-SNF) to remodel nucleosomes
whose tails have been cleaved through a limited trypsin digestion. We
show that hSWI-SNF is able to remodel tailless mononucleosomes and
nucleosomal arrays, although hSWI-SNF remodeling of tailless nucleosomes is less effective than remodeling of nucleosomes with tails. Analogous to previous observations with tailed nucleosomal templates, we show both (i) that hSWI-SNF-remodeled trypsinized mononucleosomes and arrays are stable for 30 min in the remodeled conformation after removal of ATP and (ii) that the remodeled tailless
mononucleosome can be isolated on a nondenaturing acrylamide gel as a
novel species. Thus, nucleosome remodeling by hSWI-SNF can occur via
interactions with a tailless nucleosome core.
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Stable Remodeling of Tailless Nucleosomes by the
Human SWI-SNF Complex
*
Corresponding author. Mailing address: Department of
Molecular Biology, Wellman 10, Massachusetts General Hospital, Boston, MA 02114. Phone: (617) 726-5990. Fax: (617) 726-5949. E-mail: kingston{at}frodo.mgh.harvard.edu.
This paper is dedicated to Veronica Blasquez in remembrance of her
guidance, encouragement, and friendship.
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