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Originally published In Press as doi:10.1074/jbc.M910206199 on May 2, 2000

J. Biol. Chem., Vol. 275, Issue 30, 23267-23272, July 28, 2000
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Histone H2A.Z Is Widely but Nonrandomly Distributed in Chromosomes of Drosophila melanogaster*

Thomas J. Leach, Maria Mazzeo, Heather L. Chotkowski, James P. Madigan, Michael G. Wotring, and Robert L. GlaserDagger

From the Wadsworth Center, New York State Department of Health and Department of Biomedical Sciences, State University of New York, Albany, New York 12201-2002

Variant histones that differ in amino acid sequence from S-phase histones are widespread in eukaryotes, yet the structural changes they cause to nucleosomes and how those changes affect relevant cellular processes have not been determined. H2A.F/Z is a highly conserved family of H2A variants. H2Av, the H2A.F/Z variant of Drosophila melanogaster, was localized in polytene chromosomes by indirect immunofluorescence and in diploid chromosomes by chromatin immunoprecipitation. H2Av was widely distributed in the genome and not limited to sites of active transcription. H2Av was present in thousands of euchromatic bands and the heterochromatic chromocenter of polytene chromosomes, and the H2Av antibody precipitated both transcribed and nontranscribed genes as well as noncoding euchromatic and heterochromatic sequences. The distribution of H2Av was not uniform. The complex banding pattern of H2Av in polytene chromosomes did not parallel the concentration of DNA, as did the pattern of immunofluorescence using H2A antibodies, and the density of H2Av measured by immunoprecipitation varied between different sequences. Of the sequences assayed, H2Av was least abundant on 1.688 satellite sequences and most abundant on the hsp70 genes. Finally, transcription caused, to an equivalent extent, both H2Av and H2A to be less tightly associated with DNA.


* This work was supported by National Institutes of Health Grant GM53476.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Dagger To whom correspondence should be addressed: Wadsworth Center, New York State Dept. of Health and Dept. of Biomedical Sciences, State University of New York, P. O. Box 22002, Albany, NY 12201-2002 Tel.: 518-473-4201; Fax: 518-474-3181; E-mail: glaser@wadsworth.org.


Copyright © 2000 by The American Society for Biochemistry and Molecular Biology, Inc.
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