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Originally published In Press as doi:10.1074/jbc.M704762200 on July 6, 2007
J. Biol. Chem., Vol. 282, Issue 36, 26623-26628, September 7, 2007
Stb3 Binds to Ribosomal RNA Processing Element Motifs That Control Transcriptional Responses to Growth in Saccharomyces cerevisiae*
Dritan Liko ,
Matthew G. Slattery , and
Warren Heideman 1
From the
Department of Biomolecular Chemistry, School of Medicine and the Department of Pharmaceutical Sciences, School of Pharmacy, University of Wisconsin, Madison, Wisconsin 53705
Transfer of quiescent Saccharomyces cerevisiae cells to fresh medium rapidly induces hundreds of genes needed for growth. A large subset of these genes is regulated via a DNA sequence motif known as the ribosomal RNA processing element (RRPE). However, no RRPE-binding proteins have been identified. We screened a panel of 6144 glutathione S-transferase-open reading frame fusions for RRPE-binding proteins and identified Stb3 as a specific RRPE-binding protein, both in vitro and in vivo. Chromatin immunoprecipitation experiments showed that glucose increases Stb3 binding to RRPE-containing promoters. Microarray experiments demonstrated that the loss of Stb3 inhibits the transcriptional response to fresh glucose, especially for genes with RRPE motifs. However, these experiments also showed that not all genes containing RRPEs were dependent on Stb3 for expression. Overall our data support a model in which Stb3 plays an important but not exclusive role in the transcriptional response to growth conditions.
Received for publication, June 11, 2007
, and in revised form, July 5, 2007.
* This work was supported by National Science Foundation Grants MCB-0235379 and MCB-0542779. 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.org) contains supplemental text and Table S1.
1 To whom correspondence should be addressed: School of Pharmacy, University of Wisconsin, 777 Highland Ave., Madison, WI 53705. Fax: 608-262-3397; E-mail: wheidema{at}wisc.edu.

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Copyright © 2007 by the American Society for Biochemistry and Molecular Biology.
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