Hap4p overexpression in glucose-grown Saccharomyces cerevisiae induces cells to enter a novel metabolic state

BackgroundMetabolic and regulatory gene networks generally tend to be stable. However, we have recently shown that overexpression of the transcriptional activator Hap4p in yeast causes cells to move to a state characterized by increased respiratory activity. To understand why overexpression of HAP4 is able to override the signals that normally result in glucose repression of mitochondrial function, we analyzed in detail the changes that occur in these cells.ResultsWhole-genome expression profiling and fingerprinting of the regulatory activity network show that HAP4 overexpression provokes changes that also occur during the diauxic shift. Overexpression of HAP4, however, primarily acts on mitochondrial function and biogenesis. In fact, a number of nuclear genes encoding mitochondrial proteins are induced to a greater extent than in cells that have passed through a normal diauxic shift: in addition to genes required for mitochondrial energy conservation they include genes encoding mitochondrial ribosomal proteins.ConclusionsWe show that overproduction of a single nuclear transcription factor enables cells to move to a novel state that displays features typical of, but clearly not identical to, other derepressed states.

[1]  Xin Chen,et al.  TRANSFAC: an integrated system for gene expression regulation , 2000, Nucleic Acids Res..

[2]  Barbara M. Bakker,et al.  Modulating the distribution of fluxes among respiration and fermentation by overexpression of HAP4 in Saccharomyces cerevisiae. , 2001, FEMS yeast research.

[3]  T. Werner,et al.  MatInd and MatInspector: new fast and versatile tools for detection of consensus matches in nucleotide sequence data. , 1995, Nucleic acids research.

[4]  W. H. Mager,et al.  Different roles for abf1p and a T-rich promoter element in nucleosome organization of the yeast RPS28A gene. , 2000, Nucleic acids research.

[5]  D. Botstein,et al.  Cluster analysis and display of genome-wide expression patterns. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[6]  D. Eide,et al.  Regulation of Zinc Homeostasis in Yeast by Binding of the ZAP1 Transcriptional Activator to Zinc-responsive Promoter Elements* , 1998, The Journal of Biological Chemistry.

[7]  H. Bussemaker,et al.  Regulatory element detection using correlation with expression , 2001, Nature Genetics.

[8]  H. Schägger,et al.  Blue native electrophoresis for isolation of membrane protein complexes in enzymatically active form. , 1991, Analytical biochemistry.

[9]  William Stafford Noble,et al.  Exploring Gene Expression Data with Class Scores , 2001, Pacific Symposium on Biocomputing.

[10]  P. Brown,et al.  Exploring the metabolic and genetic control of gene expression on a genomic scale. , 1997, Science.

[11]  L. Grivell,et al.  A region of the C-terminal part of the 11-kDa subunit of ubiquinol-cytochrome-c oxidoreductase of the yeast Saccharomyces cerevisiae contributes to the structure of the Qout reaction domain. , 1993, European journal of biochemistry.

[12]  D. Botstein,et al.  Genome-wide characterization of the Zap1p zinc-responsive regulon in yeast. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[13]  J. Pringle Staining of bud scars and other cell wall chitin with calcofluor. , 1991, Methods in enzymology.

[14]  H. Mewes,et al.  The 2‐(dimethylaminostyryl)‐1‐methylpyridinium cation as indicator of the mitochondrial membrane potential , 1981, FEBS letters.

[15]  G. Fink,et al.  Yeast plasma membrane ATPase is essential for growth and has homology with (Na+ + K+), K+- and Ca2+-ATPases , 1986, Nature.

[16]  Yudong D. He,et al.  Functional Discovery via a Compendium of Expression Profiles , 2000, Cell.

[17]  Stuart L. Schreiber,et al.  Partitioning the transcriptional program induced by rapamycin among the effectors of the Tor proteins , 2000, Current Biology.

[18]  D. Botstein,et al.  Genomic expression programs in the response of yeast cells to environmental changes. , 2000, Molecular biology of the cell.

[19]  A. Wagner Robustness against mutations in genetic networks of yeast , 2000, Nature Genetics.

[20]  T. Mason,et al.  Structure and regulation of a nuclear gene in Saccharomyces cerevisiae that specifies MRP13, a protein of the small subunit of the mitochondrial ribosome , 1988, Molecular and cellular biology.

[21]  D. Botstein,et al.  Systematic changes in gene expression patterns following adaptive evolution in yeast. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[22]  L. Grivell,et al.  Redirection of the Respiro-Fermentative Flux Distribution in Saccharomyces cerevisiae by Overexpression of the Transcription Factor Hap4p , 2000, Applied and Environmental Microbiology.

[23]  J. Bereiter-Hahn,et al.  Dimethylaminostyrylmethylpyridiniumiodine (daspmi) as a fluorescent probe for mitochondria in situ. , 1976, Biochimica et biophysica acta.

[24]  Hans-Werner Mewes,et al.  MIPS: a database for protein sequences, homology data and yeast genome information , 1997, Nucleic Acids Res..

[25]  K. Isono,et al.  Cloning and analysis of the nuclear gene for YmL33, a protein of the large subunit of the mitochondrial ribosome in Saccharomyces cerevisiae , 1991, Journal of bacteriology.

[26]  J. Collado-Vides,et al.  A web site for the computational analysis of yeast regulatory sequences , 2000, Yeast.

[27]  L. Grivell,et al.  Prohibitins act as a membrane‐bound chaperone for the stabilization of mitochondrial proteins , 2000, The EMBO journal.