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PMID: 14624238 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Partially phosphorylated Pho4 activates transcription of a subset of phosphate-responsive genes.

PLoS biology ·Vol. 1 ·No. 2 ·2003-11-00 ·Pages E28

Springer M, Wykoff DD, Miller N, O'Shea EK

Abstract

A cell's ability to generate different responses to different levels of stimulus is an important component of an adaptive environmental response. Transcriptional responses are frequently controlled by transcription factors regulated by phosphorylation. We demonstrate that differential phosphorylation of the budding yeast transcription factor Pho4 contributes to differential gene expression. When yeast cells are grown in high-phosphate growth medium, Pho4 is phosphorylated on four critical residues by the cyclin-CDK complex Pho80-Pho85 and is inactivated. When yeast cells are starved for phosphate, Pho4 is dephosphorylated and fully active. In intermediate-phosphate conditions, a form of Pho4 preferentially phosphorylated on one of the four sites accumulates and activates transcription of a subset of phosphate-responsive genes. This Pho4 phosphoform binds differentially to phosphate-responsive promoters and helps to trigger differential gene expression. Our results demonstrate that three transcriptional outputs can be generated by a pathway whose regulation is controlled by one kinase, Pho80-Pho85, and one transcription factor, Pho4. Differential phosphorylation of Pho4 by Pho80-Pho85 produces phosphorylated forms of Pho4 that differ in their ability to activate transcription, contributing to multiple outputs.

MeSH Terms
Blotting, Northern Blotting, Western Chromatin Immunoprecipitation Culture Media/chemistry,metabolism Cyclin-Dependent Kinases/genetics,physiology Cyclins/genetics,physiology DNA, Complementary/metabolism DNA-Binding Proteins/genetics,physiology Gene Expression Regulation, Fungal Genes, Fungal Microscopy, Fluorescence Models, Biological Models, Genetic Molecular Sequence Data Oligonucleotide Array Sequence Analysis Phosphates/chemistry Phosphopeptides/chemistry Phosphorylation Promoter Regions, Genetic Protein Binding Repressor Proteins/genetics,physiology Saccharomyces cerevisiae/metabolism Saccharomyces cerevisiae Proteins/genetics,physiology Transcription Factors/genetics,metabolism,physiology Transcription, Genetic
Chemicals
Culture Media Cyclins DNA, Complementary DNA-Binding Proteins PHO4 protein, S cerevisiae PHO80 protein, S cerevisiae Phosphates Phosphopeptides Repressor Proteins Saccharomyces cerevisiae Proteins Transcription Factors Cyclin-Dependent Kinases PHO85 protein, S cerevisiae
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Springer Michael
Howard Hughes Medical Institute, Department of Biochemistry and Biophysics, University of California, San Francisco, USA.
Wykoff Dennis D
Miller Nicole
O'Shea Erin K
Conflict of Interest

The authors have declared that no conflicts of interest exist.

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Article Info
Journal
PLoS biology
Abbr.
PLoS Biol
ISSN
1545-7885
Published
2003-11-00
Epub
2003-00-17
Pages
E28
Language
English
Region
United States
NLM ID
101183755
PMCID
PMC261874
Subset
IM
Grants
NIGMS NIH HHS · F32 GM019734 · United States
NIGMS NIH HHS · F32 GM020762 · United States
NIGMS NIH HHS · GM51377 · United States
NIGMS NIH HHS · GM20762 · United States
NIGMS NIH HHS · GM19734 · United States
NIGMS NIH HHS · R01 GM051377 · United States
Databases
RefSeq
NP_009434, NP_009651, NP_010177, NP_010622, NP_010769, NP_012087, NP_013583, NP_014039, NP_014642, NP_015294, NP_116614, NP_116692
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