Skip Navigation

This Article
Right arrow Print PDF (9554K)
Right arrow A corrigendum has been published
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (37)
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Barbaric, S.
Right arrow Articles by Hoörz, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Barbaric, S.
Right arrow Articles by Hoörz, W.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1992, Vol. 20, No. 5 1031-1038
© 1992


MOLECULAR BIOLOGY

Activation of the weakly regulated PHO8 promoter in S.cerevisiae: chromatin transition and binding sites for the positive regulatory protein PHO4

Slobodan Barbaric+, Klaus-D. Fascher§ and Wolfram Hoörz*

Institut fUÜr Physiologische Chemie, Universitat Munchen, Schillerstra(eqn)te 44 8000 Munchen 2, FRG

*To whom correspondence should be addressed

Received December 20, 1991. Revised January 31, 1992. Accepted January 31, 1992.

PHO8 encodes an alkaline phosphatase in Saccharomyces cerevisiae whose transcription is regulated by the phosphate concentration in the medium. This occurs through the action of several positive and negative regulatory proteins, also involved in the regulation of other members of the phosphatase gene family. A central role is played by PH04, the gene encoding a DNA binding regulatory protein. Digestion experiments with DNasel, micrococcal nuclease and 20 different restriction nucleases show that under conditions of PHO8 repression, there is a highly ordered chromatin structure at the promoter consisting of three hypersensitive regions, approximately 820 to 690, 540 to 510, and 230 to 160 bp upstream of the initiation codon. These hypersensitive sites are surrounded by DNA organized in nucleosomes. Gel shift analysis and in vitro footprlnting revealed the presence of two PHO4 binding sites at the PH08 promoter: a low affinity site at – 728 and a high affinity site at –532. Each one is located within a hypersensitive site. Upon derepression of PHO8, the chromatin structure changes significantly: The two upstream hypersensitive sites containing the PHO4 binding sites merge, resulting in a long region of hypersensitivity. This transition is PHO4 dependent. However, not all of the promoter becomes nucleosome free. Instead, as a novel feature, regions of intermediate accessibility are generated upstream and downstream of the third hypersensitive site, the latter region encompassing the TATA-box. The available data fit best into a concept that these regions are organized in unstable or partly unfolded nucleosomes.


+Present addresses:Laboratory of Biochemistry, Faculty of Biotechnology, Pierottijeva 6, 4I000 Zagreb, Yugoslavia

§Present addresses:Regierung von Oberfranken, Ludwigstra(eqn)e 20, 8580 Bayreuth, FRG


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
S. Barbaric, T. Luckenbach, A. Schmid, D. Blaschke, W. Horz, and P. Korber
Redundancy of Chromatin Remodeling Pathways for the Induction of the Yeast PHO5 Promoter in Vivo
J. Biol. Chem., September 21, 2007; 282(38): 27610 - 27621.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
P. Korber, S. Barbaric, T. Luckenbach, A. Schmid, U. J. Schermer, D. Blaschke, and W. Horz
The Histone Chaperone Asf1 Increases the Rate of Histone Eviction at the Yeast PHO5 and PHO8 Promoters
J. Biol. Chem., March 3, 2006; 281(9): 5539 - 5545.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
C. B. Hertel, G. Langst, W. Horz, and P. Korber
Nucleosome Stability at the Yeast PHO5 and PHO8 Promoters Correlates with Differential Cofactor Requirements for Chromatin Opening
Mol. Cell. Biol., December 15, 2005; 25(24): 10755 - 10767.
[Abstract] [Full Text] [PDF]


Home page
Eukaryot CellHome page
I. Garcia, R. Gonzalez, D. Gomez, and C. Scazzocchio
Chromatin Rearrangements in the prnD-prnB Bidirectional Promoter: Dependence on Transcription Factors
Eukaryot. Cell, February 1, 2004; 3(1): 144 - 156.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
C. D. Carvin, A. Dhasarathy, L. B. Friesenhahn, W. J. Jessen, and M. P. Kladde
Targeted cytosine methylation for in vivo detection of protein-DNA interactions
PNAS, June 24, 2003; 100(13): 7743 - 7748.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
S. Barbaric, H. Reinke, and W. Horz
Multiple Mechanistically Distinct Functions of SAGA at the PHO5 Promoter
Mol. Cell. Biol., May 15, 2003; 23(10): 3468 - 3476.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
S. Barbaric, M. Münsterkötter, C. Goding, and W. Hörz
Cooperative Pho2-Pho4 Interactions at the PHO5 Promoter Are Critical for Binding of Pho4 to UASp1 and for Efficient Transactivation by Pho4 at UASp2
Mol. Cell. Biol., May 1, 1998; 18(5): 2629 - 2639.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
D. Lohr
Nucleosome Transactions on the Promoters of the Yeast GAL and PHO Genes
J. Biol. Chem., October 24, 1997; 272(43): 26795 - 26798.
[Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. Munsterkotter, S. Barbaric, and W. Horz
Transcriptional Regulation of the Yeast PHO8 Promoter in Comparison to the Coregulated PHO5 Promoter
J. Biol. Chem., July 21, 2000; 275(30): 22678 - 22685.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.