Journal of Biological Chemistry
Volume 279, Issue 3, 16 January 2004, Pages 1867-1871
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Genes: Structure and Regulation
Deubiquitination of Histone H2B by a Yeast Acetyltransferase Complex Regulates Transcription*

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Post-translational modifications of the histone protein components of eukaryotic chromatin play an important role in the regulation of chromatin structure and gene expression (1). Given the requirement of Rad6/Bre1-dependent ubiquitination of histone H2B for H3 dimethylation (at lysines 4 and 79) and gene silencing (27), removal of ubiquitin from H2B may have a significant regulatory effect on transcription. Here we show that a putative deubiquitinating enzyme, Ubp8, is a structurally nonessential component of both the Spt-Ada-Gcn5-acetyltransferase (SAGA) and SAGA-like (SLIK) histone acetyltransferase (HAT) complexes in yeast. Disruption of this gene dramatically increases the cellular level of ubiquitinated-H2B, and SAGA and SLIK are shown to have H2B deubiquitinase activity. These findings demonstrate, for the first time, how the ubiquitin moiety can be removed from histone H2B in a regulated fashion. Ubp8 is required for full expression of the SAGA- and SLIK-dependent gene GAL10 and is recruited to the upstream activation sequence (UAS) of this gene under activating conditions, while Rad6 dissociates. Furthermore, trimethylation of H3 at lysine 4 within the UAS increases significantly under activating conditions, and remarkably, Ubp8 is shown to have a role in regulating the methylation status of this residue. Collectively, these data suggest that the SAGA and SLIK HAT complexes can regulate an integrated set of multiple histone modifications, counteracting repressive effects that alter chromatin and regulate gene expression.

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This work was supported by NIDDK, National Institutes of Health (NIH) Grant DK58646 (awarded to P. A. G.), Grant RR11823-03 (to the National Center for Research Resources Yeast Center), National Science Foundation Science and Technology Center Grant BIR9214821AM (to J. R. Y.), and grants from the National Center for Research Resources (to C. D. A.). The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The on-line version of this article (available at http://www.jbc.com) contains a Supplemental Figure.

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Supported by a postdoctoral cancer training grant from the University of Virginia Cancer Center.

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Current address: Dept. of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232.

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Current address: Laboratory of Chromatin Biology, The Rockefeller University, New York, NY 10021.