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Science 3 December 1993:
Vol. 262. no. 5139, pp. 1563 - 1566
DOI: 10.1126/science.8248805

Articles

Science, Vol 262, Issue 5139, 1563-1566
Copyright © 1993 by American Association for the Advancement of Science


articles

Nucleosome disruption by transcription factor binding in yeast

RH Morse

Laboratory of Cellular and Developmental Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892.

Studies in vivo and in vitro have shown that the packaging of DNA into chromatin can affect gene expression. Here, binding of the yeast transcriptional activator GAL4 to DNA in chromatin has been investigated in vivo with a yeast episome. A positioned nucleosome that is present in cells grown in glucose and contains a single GAL4 binding site is disrupted by GAL4 binding in galactose. GAL4 can also bind to DNA in chromatin when the carboxyl-terminal activation domain of GAL4 is either masked by GAL80 or is absent. These results show that a transcription factor can bind to its site in vivo in what would appear to be a repressive chromatin structure.


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GCN5 Dependence of Chromatin Remodeling and Transcriptional Activation by the GAL4 and VP16 Activation Domains in Budding Yeast.
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Artificially Recruited TATA-Binding Protein Fails To Remodel Chromatin and Does Not Activate Three Promoters That Require Chromatin Remodeling.
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Increased recruitment of TATA-binding protein to the promoter by transcriptional activation domains in vivo.
C Klein and K Struhl (1994)
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Stimulation of GAL4 derivative binding to nucleosomal DNA by the yeast SWI/SNF complex.
J Cote, J Quinn, J. Workman, and C. Peterson (1994)
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The N-terminal and C-terminal Domains of RAP1 Are Dispensable for Chromatin Opening and GCN4-mediated HIS4 Activation in Budding Yeast.
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