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Complete List of publications and datasets
Brief Description# of ConditionsFull DescriptionFirst AuthorAll AuthorsPublication TitleJournalYearPubMed ID
rsc3/rsc30 knockouts8DNA microarray analysis with rsc3 or rsc30 mutants reveals different effects on the expression levels of ribosomal protein genes and cell wall genesAngus-Hill MLAngus-Hill ML, Schlichter A, Roberts D, Erdjument-Bromage H, Tempst P, Cairns BRA Rsc3/Rsc30 zinc cluster dimer reveals novel roles for the chromatin remodeler RSC in gene expression and cell cycle control.Mol Cell200111336698
slt2/swi4/swi6/bck1 knockouts5Transcriptional coregulation by the cell integrity mitogen-activated protein kinase Slt2 and the cell cycle regulator Swi4Baetz KBaetz K, Moffat J, Haynes J, Chang M, Andrews BTranscriptional coregulation by the cell integrity mitogen-activated protein kinase Slt2 and the cell cycle regulator Swi4.Mol Cell Biol200111533240
splitomicin exposure and sir2 mutants7Identification of a small molecule inhibitor of Sir2pBedalov ABedalov A, Gatbonton T, Irvine WP, Gottschling DE, Simon JAIdentification of a small molecule inhibitor of Sir2p.Proc Natl Acad Sci U S A200111752457
Oxidative stress and glutaredoxin 5-deficient mutant9Transcriptome analysis of glutaredoxin 5-deficient (grx5) mutant, a model for continuous moderate oxidative stress. Respiratory petite (pet117) mutants and wild type also examined.Belli GBelli G, Molina MM, Garcia-Martinez J, Perez-Ortin JE, Herrero ESaccharomyces cerevisiae glutaredoxin 5-deficient cells subjected to continuous oxidizing conditions are affected in the expression of specific sets of genes.J Biol Chem200414722110
Histone deacetylase (rpd3/sin3/hda1 deletions)6Here, we present transcription profiles of the yeast deletion strains rpd3, sin3, sap30, ume6, hda1, hos2, and hos3. In addition, we present profiles of wild-type yeast treated with TSA in concentration- and time-dependent mannersBernstein BEBernstein BE, Tong JK, Schreiber SLGenomewide studies of histone deacetylase function in yeast.Proc Natl Acad Sci U S A200011095743
Histone deacetylase (sin3/sap30/ume6/hda1/hos2/hos3 deletions)7Here, we present transcription profiles of the yeast deletion strains rpd3, sin3, sap30, ume6, hda1, hos2, and hos3. In addition, we present profiles of wild-type yeast treated with TSA in concentration- and time-dependent mannersBernstein BEBernstein BE, Tong JK, Schreiber SLGenomewide studies of histone deacetylase function in yeast.Proc Natl Acad Sci U S A200011095743
Trichostatin A treatment time course5Here, we present transcription profiles of the yeast deletion strains rpd3, sin3, sap30, ume6, hda1, hos2, and hos3. In addition, we present profiles of wild-type yeast treated with TSA in concentration- and time-dependent mannersBernstein BEBernstein BE, Tong JK, Schreiber SLGenomewide studies of histone deacetylase function in yeast.Proc Natl Acad Sci U S A200011095743
leu3 mutant expression profiles12Analysis of leu3 mutant grown in either limited ethanol or limited ammonium media. Leu3p regulates a gene involved in nitrogen assimilation and six genes involved in branched chain amino acid metabolism. Results provide insight into the role of Leu3p in gene regulation.Boer VMBoer VM, Daran JM, Almering MJ, de Winde JH, Pronk JTContribution of the Saccharomyces cerevisiae transcriptional regulator Leu3p to physiology and gene expression in nitrogen- and carbon-limited chemostat cultures.FEMS Yeast Res200515949974
Diauxic shift time course (Batch1)13Time course of batch growth. Reference (channel 1) was a culture grown in MD medium with 2.4 g/L glucose, with 5 slpm air-flow, stirring at 400 rpm and a constant 300C temperature, dilution 0.25 volumes/hour. The experimental (channel 2) time course samples were grown in batch for the indicated time. The Low-D chemostat vs. High-D chemostat hybridization's channel 2 sample was grown in a chemostat, with a dilution rate of 0.05 volumes/hour; it is most similar to the time course samples taken between 8 and 9 hours.Brauer MJBrauer MJ, Saldanha AJ, Dolinski K, Botstein DHomeostatic adjustment and metabolic remodeling in glucose-limited yeast cultures.Mol Biol Cell200515758028
Diauxic shift time course (Batch2)7Time course of batch growth. Reference (channel 1) was a culture grown in MD medium with 2.4 g/L glucose, with 5 slpm air-flow, stirring at 400 rpm and a constant 300C temperature, dilution 0.25 volumes/hour. The experimental (channel 2) samples were grown in batch for the indicated time.Brauer MJBrauer MJ, Saldanha AJ, Dolinski K, Botstein DHomeostatic adjustment and metabolic remodeling in glucose-limited yeast cultures.Mol Biol Cell200515758028
Transcriptional regulation (I)40several crosses of BY4716 and wild wine strainBrem RBBrem RB, Yvert G, Clinton R, Kruglyak LGenetic dissection of transcriptional regulation in budding yeast.Science200211923494
Transcriptional regulation (I)(dye swap)40several crosses of BY4716 and wild wine strainBrem RBBrem RB, Yvert G, Clinton R, Kruglyak LGenetic dissection of transcriptional regulation in budding yeast.Science200211923494
Transcriptional regulation (II)12independent cultures of BY4716 and wild strains against a reference pool of BY4716Brem RBBrem RB, Yvert G, Clinton R, Kruglyak LGenetic dissection of transcriptional regulation in budding yeast.Science200211923494
Transcriptional regulation (II)(dye swap)11independent cultures of BY4716 and wild strains against a reference pool of BY4716Brem RBBrem RB, Yvert G, Clinton R, Kruglyak LGenetic dissection of transcriptional regulation in budding yeast.Science200211923494
Genetic variation in gene expression among parents and progenies (dye-swap)131Expression profiling of parental strains and 112 haploid progenies from a cross of strain BY4716 and the wild wine strain RM11-1a. Results used to find linkage between gene expression levels, which are treated as quantitative traits, and genetic markers.Brem RBBrem RB, Kruglyak LThe landscape of genetic complexity across 5,700 gene expression traits in yeast.Proc Natl Acad Sci U S A200515659551
Genetic variation in gene expression among parents and progenies131Expression profiling of parental strains and 112 haploid progenies from a cross of strain BY4716 and the wild wine strain RM11-1a. Results used to find linkage between gene expression levels, which are treated as quantitative traits, and genetic markers.Brem RBBrem RB, Kruglyak LThe landscape of genetic complexity across 5,700 gene expression traits in yeast.Proc Natl Acad Sci U S A200515659551
Lithium response7Wild type CEN.PK113-7D grown with 20 g/L galactose. LiCl (10 mM, therapeutically relevant) added and samples analyzed at 0, 20, 40, 60 and 140 minutes after LiCl addition. Lithium inhibits phosphoglucomutase, affecting galactose uptake and growth.Bro CBro C, Regenberg B, Lagniel G, Labarre J, Montero-Lomeli M, Nielsen JTranscriptional, proteomic, and metabolic responses to lithium in galactose-grown yeast cells.J Biol Chem200312791685
Chitin synthesis11wt and fks1 mutant exposed to chitin-inducing glucosamine for 2-hours or continuous steady stateBulik DABulik DA, Olczak M, Lucero HA, Osmond BC, Robbins PW, Specht CAChitin synthesis in Saccharomyces cerevisiae in response to supplementation of growth medium with glucosamine and cell wall stress.Eukaryot Cell200314555471
Genotoxic stress24BY4730 cells treated with DNA-reactive compounds cisplatin, methyl methanesulfonate (MMS), and bleomycin to induce genotoxic stress. Effect of genotoxic compounds compared to cytotoxic compounds, NaCl and ethanol.Caba ECaba E, Dickinson DA, Warnes GR, Aubrecht JDifferentiating mechanisms of toxicity using global gene expression analysis in Saccharomyces cerevisiae.Mutat Res200515878181
H2O2 exposure to wt and Deltatrr1 knockout15Role of thioredoxin reductase in the Yap1p-dependent response to oxidative stress in Saccharomyces cerevisiae.Carmel-Harel OCarmel-Harel O, Stearman R, Gasch AP, Botstein D, Brown PO, Storz GRole of thioredoxin reductase in the Yap1p-dependent response to oxidative stress in Saccharomyces cerevisiae.Mol Microbiol200111169101
pho85 inhibition12we used a chemical genetic approach that enabled us to control Pho85 kinase activity with a cell-permeable inhibitor and whole genome transcript profiling.Carroll ASCarroll AS, Bishop AC, DeRisi JL, Shokat KM, O'Shea EKChemical inhibition of the Pho85 cyclin-dependent kinase reveals a role in the environmental stress response.Proc Natl Acad Sci U S A200111675494
Unfolded protein response2DNA microarray assays to examine whether the expression of H-2Kb increases the transcription of genes also induced by the UPR. mRNA was harvested from wild-type cells that either express H-2Kb or bear a control plasmidCasagrande RCasagrande R, Stern P, Diehn M, Shamu C, Osario M, Zuniga M, Brown PO, Ploegh HDegradation of proteins from the ER of S. cerevisiae requires an intact unfolded protein response pathway.Mol Cell200010882108
acid response11response to various changes in extracellular environment, including changes in temperature, oxidation, nutrients, pH, and osmolarityCauston HCCauston HC, Ren B, Koh SS, Harbison CT, Kanin E, Jennings EG, Lee TI, True HL, Lander ES, Young RARemodeling of yeast genome expression in response to environmental changes.Mol Biol Cell200111179418
alkali response8response to various changes in extracellular environment, including changes in temperature, oxidation, nutrients, pH, and osmolarityCauston HCCauston HC, Ren B, Koh SS, Harbison CT, Kanin E, Jennings EG, Lee TI, True HL, Lander ES, Young RARemodeling of yeast genome expression in response to environmental changes.Mol Biol Cell200111179418
heat response7response to various changes in extracellular environment, including changes in temperature, oxidation, nutrients, pH, and osmolarityCauston HCCauston HC, Ren B, Koh SS, Harbison CT, Kanin E, Jennings EG, Lee TI, True HL, Lander ES, Young RARemodeling of yeast genome expression in response to environmental changes.Mol Biol Cell200111179418
NaCl response6response to various changes in extracellular environment, including changes in temperature, oxidation, nutrients, pH, and osmolarityCauston HCCauston HC, Ren B, Koh SS, Harbison CT, Kanin E, Jennings EG, Lee TI, True HL, Lander ES, Young RARemodeling of yeast genome expression in response to environmental changes.Mol Biol Cell200111179418
peroxide response7response to various changes in extracellular environment, including changes in temperature, oxidation, nutrients, pH, and osmolarityCauston HCCauston HC, Ren B, Koh SS, Harbison CT, Kanin E, Jennings EG, Lee TI, True HL, Lander ES, Young RARemodeling of yeast genome expression in response to environmental changes.Mol Biol Cell200111179418
Sorbitol response6response to various changes in extracellular environment, including changes in temperature, oxidation, nutrients, pH, and osmolarityCauston HCCauston HC, Ren B, Koh SS, Harbison CT, Kanin E, Jennings EG, Lee TI, True HL, Lander ES, Young RARemodeling of yeast genome expression in response to environmental changes.Mol Biol Cell200111179418
TBP inhibition20Here, we use DNA microarrays to explore the genome-wide interplay of several TBP-interacting inhibitors in the yeast Saccharomyces cerevisiaeChitikila CChitikila C, Huisinga KL, Irvin JD, Basehoar AD, Pugh BFInterplay of TBP inhibitors in global transcriptional control.Mol Cell200212419230
mitotic cell cycle17Cell-cycle arrested yeast cells are synchronized by being held at a restrictive temperature and then released at t=0. RNA expression via Affymetrix chips is measured every 10 minutes until t=160. Data up to t=40 reflects temperature-induced as well as cell-cycle effects.Cho RJCho RJ, Campbell MJ, Winzeler EA, Steinmetz L, Conway A, Wodicka L, Wolfsberg TG, Gabrielian AE, Landsman D, Lockhart DJ, Davis RWA genome-wide transcriptional analysis of the mitotic cell cycle.Mol Cell19989702192
Sporulation time course7Samples taken during sporulation up to 11 hoursChu SChu S, DeRisi J, Eisen M, Mulholland J, Botstein D, Brown PO, Herskowitz IThe transcriptional program of sporulation in budding yeast.Science19989784122
mRNA processing factors and splicing (dye swap)17brr1, cus2, dbr1, ecm2, gcr3, hsp104, msl1, mud1, mud13, mud2, nam8, prp17, prp18, snu17, snu40, snu66, upf3 deletion mutantsClark TAClark TA, Sugnet CW, Ares MGenomewide analysis of mRNA processing in yeast using splicing-specific microarrays.Science200211988574
mRNA processing factors and splicing17brr1, cus2, dbr1, ecm2, gcr3, hsp104, msl1, mud1, mud13, mud2, nam8, prp17, prp18, snu17, snu40, snu66, upf3 deletion mutantsClark TAClark TA, Sugnet CW, Ares MGenomewide analysis of mRNA processing in yeast using splicing-specific microarrays.Science200211988574
yap1 and yap2 knockouts with peroxide and cadmium added11There is a separate summary series for each strain and treatment combination. These include wild type control, with peroxide and with cadmium, yap1 knockout control and with peroxide and with cadmium, yap2 knockout control and with peroxide and with cadmium, double knockouts control and with peroxide, wild type and fold change numbers from wild type control for each strain and treatment.Cohen BACohen BA, Pilpel Y, Mitra RD, Church GMDiscrimination between paralogs using microarray analysis: application to the Yap1p and Yap2p transcriptional networks.Mol Biol Cell200212006656
Osmotic stress12Comparison of wild type and rpd3- S. cerevisiae cells in response to osmotic stress. Wild type (MATalpha ura3 leu2 his3) and rpd3- (MATalpha ura3 leu2 his3 rpd3::KANMX) were grown to OD660=1 in YPD media and then subjected or not to a brief osmotic stress (5 or 20 min / 0.4 M NaCl). Cells were collected by centrifugation and total RNA was extracted as described.De Nadal EDe Nadal E, Zapater M, Alepuz PM, Sumoy L, Mas G, Posas FThe MAPK Hog1 recruits Rpd3 histone deacetylase to activate osmoresponsive genes.Nature200414737171
Diauxic shift time course7Samples of expression taken at several time points during the metabolic shift from anaerobic fermentation to aerobic respiration.DeRisi JLDeRisi JL, Iyer VR, Brown POExploring the metabolic and genetic control of gene expression on a genomic scale.Science19979381177
post heat shock, delayed rapamycin exposure time course20we have examined the role of the essential protein Tap42 in transcriptional regulation by TorDuvel KDuvel K, Santhanam A, Garrett S, Schneper L, Broach JRMultiple roles of Tap42 in mediating rapamycin-induced transcriptional changes in yeast.Mol Cell200312820961
post heat shock, immediate rapamycin exposure time course10we have examined the role of the essential protein Tap42 in transcriptional regulation by TorDuvel KDuvel K, Santhanam A, Garrett S, Schneper L, Broach JRMultiple roles of Tap42 in mediating rapamycin-induced transcriptional changes in yeast.Mol Cell200312820961
Mitochondrial dysfunction11We used DNA microarrays to characterize the transcriptional responses to different mitochondrial perturbations in Saccharomyces cerevisiae.Epstein CBEpstein CB, Waddle JA, Hale W, Dave V, Thornton J, Macatee TL, Garner HR, Butow RAGenome-wide responses to mitochondrial dysfunction.Mol Biol Cell200111179416
SPT10 global transcription regulator null mutant6Expression profiling of mutants lacking Spt10p. Spt10p binds the upstream activating sequences in all major core histone promoters. Results provide insight into the mechanism by which Spt10p acts as a global regulator of transcription.Eriksson PREriksson PR, Mendiratta G, McLaughlin NB, Wolfsberg TG, Marino-Ramirez L, Pompa TA, Jainerin M, Landsman D, Shen CH, Clark DJGlobal regulation by the yeast Spt10 protein is mediated through chromatin structure and the histone upstream activating sequence elements.Mol Cell Biol200516199888
Evolved strains4Beginning with a clonal, founding population, independently evolved strains were obtained from three independent cultures after continuous aerobic growth in glucose-limited chemostats for more than 250 generations. DNA microarrays were used to compare genome-wide patterns of gene expression in the evolved strains and the parental strain.Ferea TLFerea TL, Botstein D, Brown PO, Rosenzweig RFSystematic changes in gene expression patterns following adaptive evolution in yeast.Proc Natl Acad Sci U S A199910449761
Hydrostatic pressure response2Gene expression patterns in response to hydrostatic pressure were determined by whole genome microarray hybridization. Functional classification of the 274 genes affected by pressure treatment of 200 MPa for 30 min revealed a stress response expression profile.Fernandes PMFernandes PM, Domitrovic T, Kao CM, Kurtenbach EGenomic expression pattern in Saccharomyces cerevisiae cells in response to high hydrostatic pressure.FEBS Lett200414706843
proteasome inhibition with exposure to PS-34130whole-genome technologies in Saccharomyces cerevisiae to determine the cellular impact of the proteasome inhibitor PS-341Fleming JAFleming JA, Lightcap ES, Sadis S, Thoroddsen V, Bulawa CE, Blackman RKComplementary whole-genome technologies reveal the cellular response to proteasome inhibition by PS-341.Proc Natl Acad Sci U S A200211830665
Aging in yeast8wt & sgs1 null, w/ or w/o MMS (DNA damaging agent)Fry RCFry RC, Sambandan TG, Rha CDNA damage and stress transcripts in Saccharomyces cerevisiae mutant sgs1.Mech Ageing Dev200312875747
Amino acid, adenine starvation 5minimal medium lacking amino acids and adenine, samples at 0, 0.5, 1, 2, 4, 6 hoursGasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Carbon sources6wt grown in YP media with 2% weight to volume of glucose, raffinose, galactose, fructose, sucrose, or ethanol as carbon sourceGasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Diamide treatment time course8Diamide (1.5 mM) added to culture, and samples recovered at several time points up to 90 minutes.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Dithiothrietol exposure time course (y13)8Dithiothrietol (DTT; 2.5 mM) added to culture and samples recovered at several time points up to 180 minutes.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Dithiothrietol exposure time course (y14)7Dithiothrietol (DTT; 2.5 mM) added to culture and samples recovered at several time points up to 480 minutes.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Hydrogen peroxide response2wt and yap1 mutant collected 20 minutes after exposure to 0.3mM hydrogren peroxideGasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Hydrogen peroxide response time course9Hydrogen peroxide (0.3 mM) added to culture and samples taken at several time points up to 160 minutes.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Heat Shock 25C to 37C time course8Heat shock from 25¡C to 37¡C. Samples collected at several time points up to 80 minutes.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Heat Shock 29C to 33C time course4Heat shock from 29¡C to 33¡C. Samples collected at 5, 15, 30 and 90 minutes.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Heat Shock 30C to 37C time course5Cultures shifted from 30¡C to 37¡C and samples collected at 0, 5, 15, 30 and 60 minutes.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Heat Shock 37C to 25C5Heat shock from 37¡C to 25¡C. Samples collected at 15, 30, 45, 60 and 90 minutes.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Mild Heat Shock6Heat shock from 29¡C to 33¡C, with or without addition of 1 M sorbitol. Samples collected at 5, 15 and 30 minutes.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Heat Shock from various temp to 37C6Samples collected 20 min after temperature shift from either 17¡C, 21¡C, 25¡C, 29¡C or 33¡C to 37¡C.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Hyper-osmotic shock time course6Samples grown in YPD supplemented with 1 M sorbitol and collected at several time points up to 60 minutes.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Hypo-osmotic shock time course5Cells resuspended in YPD medium without sorbitol. Samples recovered at 5, 15, 30, 45 and 60 minutes.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Menadione exposure time course9Superoxide-generating drug menadione bisulphate (1 mM) added to culture and samples removed at several time points up to 160 minutes.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Nitrogen depletion time course9Samples grown in minimal medium without amino acids or adenine, low ammonium sulfate and collected at various time points up to 3 days.Gasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Stationary phase time course (y12)10Culture grown to OD600 0.3 after which samples collected at various time points up to 13 daysGasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Stationary phase time course (y14)9Culture grown to OD600 0.3 after which samples collected at various time points up to 13 daysGasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Steady-state temperature (y13)5Samples collected from cells grown continuously at 17¡C, 21¡C, 25¡C, 29¡C and 37¡C, and compared to cells grown at 33¡CGasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Steady-state temperature (y14)8Samples collected from cells grown continuously at 15¡C, 17¡C, 21¡C, 25¡C, 29¡C, 33¡C and 36¡CGasch APGasch AP, Spellman PT, Kao CM, Carmel-Harel O, Eisen MB, Storz G, Botstein D, Brown POGenomic expression programs in the response of yeast cells to environmental changes.Mol Biol Cell200011102521
Copper regulon6Growth conditions of excess copper or copper deficiency, regulated by Mac1 or Ace1 transcriptional activators.Gross CGross C, Kelleher M, Iyer VR, Brown PO, Winge DRIdentification of the copper regulon in Saccharomyces cerevisiae by DNA microarrays.J Biol Chem200010922376
rapamycin exposure14We measured the immediate transcriptional response of yeast grown in rich media and treated with rapamycin to investigate the direct effects of Tor proteins on nutrient-sensitive signaling pathwaysHardwick JSHardwick JS, Kuruvilla FG, Tong JK, Shamji AF, Schreiber SLRapamycin-modulated transcription defines the subset of nutrient-sensitive signaling pathways directly controlled by the Tor proteins.Proc Natl Acad Sci U S A199910611304
pho85 related knockouts20DNA microarrays to examine the genome-wide transcriptional consequences of deleting PHO85 or members of the Pho85 cyclin familyHuang DHuang D, Moffat J, Andrews BDissection of a complex phenotype by functional genomics reveals roles for the yeast cyclin-dependent protein kinase Pho85 in stress adaptation and cell integrity.Mol Cell Biol200212077337
diverse knockout mutants300300 knockout mutants create a compendium of expression profilesHughes TRHughes TR, Marton MJ, Jones AR, Roberts CJ, Stoughton R, Armour CD, Bennett HA, Coffey E, Dai H, He YD, Kidd MJ, King AM, Meyer MR, Slade D, Lum PY, Stepaniants SB, Shoemaker DD, Gachotte D, Chakraburtty K, Simon J, Bard M, Friend SHFunctional discovery via a compendium of expression profiles.Cell200010929718
GAL mutants21systematic perturbations of the yeast galactose-utilization pathwayIdeker TIdeker T, Thorsson V, Ranish JA, Christmas R, Buhler J, Eng JK, Bumgarner R, Goodlett DR, Aebersold R, Hood LIntegrated genomic and proteomic analyses of a systematically perturbed metabolic network.Science200111340206
SBF-MBF genomic distribution (ORF_intergenic_v1.0) (I)2Identification of genomic binding sites of the sequence-specific transcription factors SBF and MBF.Iyer VRIyer VR, Horak CE, Scafe CS, Botstein D, Snyder M, Brown POGenomic binding sites of the yeast cell-cycle transcription factors SBF and MBF.Nature200111206552
SBF-MBF genomic distribution (ORF_intergenic_v1.0) (II)2Identification of genomic binding sites of the sequence-specific transcription factors SBF and MBF.Iyer VRIyer VR, Horak CE, Scafe CS, Botstein D, Snyder M, Brown POGenomic binding sites of the yeast cell-cycle transcription factors SBF and MBF.Nature200111206552
SBF-MBF genomic distribution (intergenic_v1.0) (I)6Identification of genomic binding sites of the sequence-specific transcription factors SBF and MBF.Iyer VRIyer VR, Horak CE, Scafe CS, Botstein D, Snyder M, Brown POGenomic binding sites of the yeast cell-cycle transcription factors SBF and MBF.Nature200111206552
SBF-MBF genomic distribution (intergenic_v1.0) (II)5Identification of genomic binding sites of the sequence-specific transcription factors SBF and MBF.Iyer VRIyer VR, Horak CE, Scafe CS, Botstein D, Snyder M, Brown POGenomic binding sites of the yeast cell-cycle transcription factors SBF and MBF.Nature200111206552
Exposure to alkylating, oxidizing agents, ionizing radiation28Exposure to carcinogenic alkylating agents, oxidizing agents, and ionizing radiation modulates transcript levels for over one third of Saccharomyces cerevisiae's 6,200 genes.Jelinsky SAJelinsky SA, Estep P, Church GM, Samson LDRegulatory networks revealed by transcriptional profiling of damaged Saccharomyces cerevisiae cells: Rpn4 links base excision repair with proteasomes.Mol Cell Biol200011027285
Xylose metabolism6Strain YSX3 engineered for D-xylose utilization and respiration-deficient mutant FPL-YSX3P were grown under full aeration or oxygen limitation, with glucose or xylose as a carbon source.Jin YSJin YS, Laplaza JM, Jeffries TWSaccharomyces cerevisiae engineered for xylose metabolism exhibits a respiratory response.Appl Environ Microbiol200415528549
Ras/cAMP signal transduction pathway (dye swap)5wt, pde2Delta deletion mutantJones DLJones DL, Petty J, Hoyle DC, Hayes A, Ragni E, Popolo L, Oliver SG, Stateva LITranscriptome profiling of a Saccharomyces cerevisiae mutant with a constitutively activated Ras/cAMP pathway.Physiol Genomics200314570984
Ras/cAMP signal transduction pathway5wt, pde2Delta deletion mutantJones DLJones DL, Petty J, Hoyle DC, Hayes A, Ragni E, Popolo L, Oliver SG, Stateva LITranscriptome profiling of a Saccharomyces cerevisiae mutant with a constitutively activated Ras/cAMP pathway.Physiol Genomics200314570984
Haa1 analysis4Microarray experiments were carried out to determine whether Haa1 is a transcription factor and to identify any potential target genes. Haa1 was found to be a transcriptional activator of a set of genes encoding membrane stress proteins.Keller GKeller G, Ray E, Brown PO, Winge DRHaa1, a protein homologous to the copper-regulated transcription factor Ace1, is a novel transcriptional activator.J Biol Chem200111504737
Carbon source shift3The global gene expression program that accompanies the adaptation of Saccharomyces cerevisiae to an abrupt transfer from a fermentable to a nonfermentable carbon source was characterized by using a cDNA microarray to monitor the relative abundances and polysomal distributions of mRNAs.Kuhn KMKuhn KM, DeRisi JL, Brown PO, Sarnow PGlobal and specific translational regulation in the genomic response of Saccharomyces cerevisiae to a rapid transfer from a fermentable to a nonfermentable carbon source.Mol Cell Biol200111154278
Unfolded protein response and HAC1 transcription13Strains expressing HAC1 grown at 30C or shifted from 23C to 37C, and treated with 6mM DTT or tunicamycin for 60 minutes. DTT and TM activate the unfolded protein response, which is regulated by Hac1p.Leber JHLeber JH, Bernales S, Walter PIRE1-independent gain control of the unfolded protein response.PLoS Biol200415314654
rnt1 null mutant expression profile9Expression profiling of isogenic strains lacking Rnt1p, a member of the RNase III family of double-stranded RNA endonucleases. Results identify potential Rnt1p mRNA targetsLee ALee A, Henras AK, Chanfreau GMultiple RNA surveillance pathways limit aberrant expression of iron uptake mRNAs and prevent iron toxicity in S. cerevisiae.Mol Cell200515989963
gcr1 mutant, glucose exposure17the genomic expression patterns of wild-type and gcr1 mutant yeast growing on various media, with and without glucoseLopez MCLopez MC, Baker HVUnderstanding the growth phenotype of the yeast gcr1 mutant in terms of global genomic expression patterns.J Bacteriol200010940042
Zinc homeostatis, zap19The Zap1p transcription factor senses cellular zinc status and increases expression of its target genes in response to zinc deficiency. Previously known Zap1p-regulated genes encode the Zrt1p, Zrt2p, and Zrt3p zinc transporter genes and Zap1p itself. To allow the characterization of additional genes in yeast important for zinc homeostasis, a systematic study of gene expression on the genome-wide scale was used to identify other Zap1p target genes. Using a combination of DNA microarrays and a computer-assisted analysis of shared motifs in the promoters of similarly regulated genes, we identified 46 genes that are potentially regulated by Zap1p. Zap1p-regulated expression of seven of these newly identified target genes was confirmed independently by using lacZ reporter fusions, suggesting that many of the remaining candidate genes are also Zap1p targets. Our studies demonstrate the efficacy of this combined approach to define the regulon of a specific eukaryotic transcription factor.Lyons TJLyons TJ, Gasch AP, Gaither LA, Botstein D, Brown PO, Eide DJGenome-wide characterization of the Zap1p zinc-responsive regulon in yeast.Proc Natl Acad Sci U S A200010884426
MAPK mutants11transcript levels in strains in which MAPK signaling was altered geneticallyMadhani HDMadhani HD, Galitski T, Lander ES, Fink GREffectors of a developmental mitogen-activated protein kinase cascade revealed by expression signatures of signaling mutants.Proc Natl Acad Sci U S A199910535956
TOR2-controlled transcription12Comparison of total transcription profiles for temperature-sensitive TOR2 mutant strain SH121 to its isogenic wild type counterpart SH100Martin DEMartin DE, Demougin P, Hall MN, Bellis MRank Difference Analysis of Microarrays (RDAM), a novel approach to statistical analysis of microarray expression profiling data.BMC Bioinformatics200415476558
immunosuppressant response7treatment of yeast mutant strains defective in calcineurin, immunophilins or other genes with the immunosuppressants cyclosporin A or FK506Marton MJMarton MJ, DeRisi JL, Bennett HA, Iyer VR, Meyer MR, Roberts CJ, Stoughton R, Burchard J, Slade D, Dai H, Bassett DE, Hartwell LH, Brown PO, Friend SHDrug target validation and identification of secondary drug target effects using DNA microarrays.Nat Med19989809554
abf1-1 mutant at 36C4abf1-1 mutant and wt cells grown at 30C, raised to 36C for 45 min. Four repeats of the same experiement.Miyake TMiyake T, Reese J, Loch CM, Auble DT, Li RGenome-wide analysis of ARS (autonomously replicating sequence) binding factor 1 (Abf1p)-mediated transcriptional regulation in Saccharomyces cerevisiae.J Biol Chem200415192094
Phosphate-regulated pathway (I)5Modifying phosphate levels through mutation (pho81c, pho85, pho80, pho4c) or chemical manipulationOgawa NOgawa N, DeRisi J, Brown PONew components of a system for phosphate accumulation and polyphosphate metabolism in Saccharomyces cerevisiae revealed by genomic expression analysis.Mol Biol Cell200011102525
Phosphate-regulated pathway (II)3Modifying phosphate levels through mutation or chemical manipulation (YPAD+Pi vs. YPAD-Pi)Ogawa NOgawa N, DeRisi J, Brown PONew components of a system for phosphate accumulation and polyphosphate metabolism in Saccharomyces cerevisiae revealed by genomic expression analysis.Mol Biol Cell200011102525
Fermentation time course12Expression of brewing yeast during production scale lager beer fermentation. Samples at time points up to 264 hours.Olesen KOlesen K, Felding T, Gjermansen C, Hansen JThe dynamics of the Saccharomyces carlsbergensis brewing yeast transcriptome during a production-scale lager beer fermentation.FEMS Yeast Res200212702272
Deubiquitinating enzyme UBP10 inactivation4Comparison of wt, ubp10 null, sir4 null, and ubp10 sir4 double null mutantsOrlandi IOrlandi I, Bettiga M, Alberghina L, Vai MTranscriptional profiling of ubp10 null mutant reveals altered subtelomeric gene expression and insurgence of oxidative stress response.J Biol Chem200414623890
HOG MAPK pathway133response to elevated osmolarityO'Rourke SMO'Rourke SM, Herskowitz IUnique and redundant roles for HOG MAPK pathway components as revealed by whole-genome expression analysis.Mol Biol Cell200414595107
Phosphomannose isomerase PMI40 deletion strain response to excess mannose15Expression profiling of a phosphomannose isomerase PMI40 deletion strain growing on media with various mannose concentrations up to 5 g/liter. Results provide insight into the cause of slow growth exhibited by the PMI40 deletion strain in media with excess mannose.Pitkanen JPPitkanen JP, Torma A, Alff S, Huopaniemi L, Mattila P, Renkonen RExcess mannose limits the growth of phosphomannose isomerase PMI40 deletion strain of Saccharomyces cerevisiae.J Biol Chem200415520001
Sporulation of two strains24meiotic expression patterns of two yeast strains, SK1 and W303, that display distinct kinetics and efficiencies of sporulationPrimig MPrimig M, Williams RM, Winzeler EA, Tevzadze GG, Conway AR, Hwang SY, Davis RW, Esposito REThe core meiotic transcriptome in budding yeasts.Nat Genet200011101837
Filamentous-form growth on solid media time course10wt diploid cells shifted from yeast-form growth in SHAD liquid with plentiful glucose and ammonium to filamentous-form growth on SLAD agar with low ammonium. Samples collected hourly for 10 hours.Prinz SPrinz S, Avila-Campillo I, Aldridge C, Srinivasan A, Dimitrov K, Siegel AF, Galitski TControl of yeast filamentous-form growth by modules in an integrated molecular network.Genome Res200414993204
Iron concentration and AFT1 overexpression4Analysis of iron-regulated gene expression in Saccharomyces cerevisiae using cDNA microarrays has identified three putative cell wall proteins that are directly regulated by Aft1p, the major iron-dependent transcription factor in yeast.Protchenko OProtchenko O, Ferea T, Rashford J, Tiedeman J, Brown PO, Botstein D, Philpott CCThree cell wall mannoproteins facilitate the uptake of iron in Saccharomyces cerevisiae.J Biol Chem200111673473
Pheremone response56Exposure of MATa to alpha-factor, MATalpha to a-factor time courses at various concentrations of pheremonesRoberts CJRoberts CJ, Nelson B, Marton MJ, Stoughton R, Meyer MR, Bennett HA, He YD, Dai H, Walker WL, Hughes TR, Tyers M, Boone C, Friend SHSignaling and circuitry of multiple MAPK pathways revealed by a matrix of global gene expression profiles.Science200010657304
TPK1, TPK2, TPK3 mutants12study of TPK1 (alternate name for YJL164C), TPK2 (alternate name for YPL203W), and TPK3 (YRL166C) mutantsRobertson LSRobertson LS, Causton HC, Young RA, Fink GRThe yeast A kinases differentially regulate iron uptake and respiratory function.Proc Natl Acad Sci U S A200010811893
sus1 mutant6wt, sus1 deletion mutantRodriguez-Navarro SRodriguez-Navarro S, Fischer T, Luo MJ, Antunez O, Brettschneider S, Lechner J, Perez-Ortin JE, Reed R, Hurt ESus1, a functional component of the SAGA histone acetylase complex and the nuclear pore-associated mRNA export machinery.Cell200414718168
fhl1 and ifh1 deletion mutants6Expression profiling of fhl1 single deletion mutant and ifh1 fhl1 double deletion mutant. Mutants generated from W303 strain. Results indicate that Ifh1p and Fhl1p function together to regulate the transcription of ribosomal protein genes.Rudra DRudra D, Zhao Y, Warner JRCentral role of Ifh1p-Fhl1p interaction in the synthesis of yeast ribosomal proteins.EMBO J200515692568
Iron homeostasis2DNA microarrays were used to identify genes regulated by AFT2Rutherford JCRutherford JC, Jaron S, Ray E, Brown PO, Winge DRA second iron-regulatory system in yeast independent of Aft1p.Proc Natl Acad Sci U S A200111734641
Histone deacetylase RPD3 deletion and histone mutations18Analysis of gene regulation by expression profiling of single mutants for histone deacetylase RPD3, histones H3 and H4, and double mutants for either RPD3 and H3 or RPD3 and H4. Histone mutants defective in amino terminal tails, which are acetylated and deacetylated in transcription regulation.Sabet NSabet N, Volo S, Yu C, Madigan JP, Morse RHGenome-wide analysis of the relationship between transcriptional regulation by Rpd3p and the histone H3 and H4 amino termini in budding yeast.Mol Cell Biol200415456858
limitation by Leucine29physiological response to limitation by leucine in batch and steady-state (chemostat) cultures of S. cerevisiaeSaldanha AJSaldanha AJ, Brauer MJ, Botstein DNutritional homeostasis in batch and steady-state culture of yeast.Mol Biol Cell200415240820
limitation by Phosphate30physiological response to limitation by phosphate in batch and steady-state (chemostat) cultures of S. cerevisiaeSaldanha AJSaldanha AJ, Brauer MJ, Botstein DNutritional homeostasis in batch and steady-state culture of yeast.Mol Biol Cell200415240820
limitation by Sulfate21physiological response to limitation by sulfate in batch and steady-state (chemostat) cultures of S. cerevisiaeSaldanha AJSaldanha AJ, Brauer MJ, Botstein DNutritional homeostasis in batch and steady-state culture of yeast.Mol Biol Cell200415240820
limitation by Uracil20physiological response to limitation by Uracil in batch and steady-state (chemostat) cultures of S. cerevisiaeSaldanha AJSaldanha AJ, Brauer MJ, Botstein DNutritional homeostasis in batch and steady-state culture of yeast.Mol Biol Cell200415240820
comparison of limitation by Ura, Sul, Pho, and Leu24physiological response to limitation by diverse nutrients in steady-state (chemostat) cultures of S. cerevisiaeSaldanha AJSaldanha AJ, Brauer MJ, Botstein DNutritional homeostasis in batch and steady-state culture of yeast.Mol Biol Cell200415240820
Pre-mRNA splicing factor mutants at restrictive temperature time course24wt, prp17 null, prp17-1, prp22-1 at time points following a temperature shift from permissive 23C to restrictive 37CSapra AKSapra AK, Arava Y, Khandelia P, Vijayraghavan UGenome-wide analysis of pre-mRNA splicing: intron features govern the requirement for the second-step factor, Prp17 in Saccharomyces cerevisiae and Schizosaccharomyces pombe.J Biol Chem200415452114
IFH1 overexpression: time course24Analysis of overexpression of essential ribosomal protein activator IFH1. Cells engineered to express IFH1 from a galactose inducible promoter. Expression examined at various time points up to 60 minutes following galactose addition. Results indicate that IFH1 regulates ribosomal protein genes.Schawalder SBSchawalder SB, Kabani M, Howald I, Choudhury U, Werner M, Shore DGrowth-regulated recruitment of the essential yeast ribosomal protein gene activator Ifh1.Nature200415616569
Heat Shock, kin82 mutant10wt and kin82 mutant strains after heat shock from 25C to 37C, samples at time points up to 1 hour.Segal ESegal E, Shapira M, Regev A, Pe'er D, Botstein D, Koller D, Friedman NModule networks: identifying regulatory modules and their condition-specific regulators from gene expression data.Nat Genet200312740579
Hypo-osmotic shock, ppt1 mutant10Temporal analysis of wild type and ppt1 mutant strains after hypo-osmotic shock. Cultures grown with 1M sorbitol for ~20 hours, then cells resuspended in YPD after which samples collected at several time points up to 1 hour.Segal ESegal E, Shapira M, Regev A, Pe'er D, Botstein D, Koller D, Friedman NModule networks: identifying regulatory modules and their condition-specific regulators from gene expression data.Nat Genet200312740579
Stationary phase, ypl230w mutant12wt, ypl230w mutant in stationary phase. Cultures were grown to OD600 of 0.27 (ypl230w) and 0.4 (wild-type), then samples collected at various time points up to 24 hoursSegal ESegal E, Shapira M, Regev A, Pe'er D, Botstein D, Koller D, Friedman NModule networks: identifying regulatory modules and their condition-specific regulators from gene expression data.Nat Genet200312740579
Iron deprivation6Saccharomyces cerevisiae responds to depletion of iron in the environmentShakoury-Elizeh MShakoury-Elizeh M, Tiedeman J, Rashford J, Ferea T, Demeter J, Garcia E, Rolfes R, Brown PO, Botstein D, Philpott CCTranscriptional remodeling in response to iron deprivation in Saccharomyces cerevisiae.Mol Biol Cell200414668481
oxidative stress responses70Oxidative stress caused by Menadione or Hydrogen peroxide in synchronized Saccharomyces cerevisiae cultures. Alpha factor synchronized cultures (0.2-0.4 OD), treated at the beginning of S phase (25 min after release from G1 arrest) with either 2 mM Menadione (MD) or 0.24 mM Hydrogen peroxide (HP), show cell cycle effects. Cells treated with MD arrested at G1. Cells treated with HP delayed at S and then, after removal of HP at 135 minutes , continued the cell cycle, only to arrest at G2/M. Growth was carried out in 30C with shaking (295 rpm).Shapira MShapira M, Segal E, Botstein DDisruption of yeast forkhead-associated cell cycle transcription by oxidative stress.Mol Biol Cell200415371544
Cell cycle, alpha-factor block-release16Culture synchronized by alpha factor arrest, then samples taken every 7 minutes as cells went through cell cycle.Spellman PTSpellman PT, Sherlock G, Zhang MQ, Iyer VR, Anders K, Eisen MB, Brown PO, Botstein D, Futcher BComprehensive identification of cell cycle-regulated genes of the yeast Saccharomyces cerevisiae by microarray hybridization.Mol Biol Cell19989843569
Cell cycle, cdc15 block-release25Culture synchronized in telophase by arrest of cdc15 temperature-sensitive mutant. Samples taken during the course of almost three full cell cycles.Spellman PTSpellman PT, Sherlock G, Zhang MQ, Iyer VR, Anders K, Eisen MB, Brown PO, Botstein D, Futcher BComprehensive identification of cell cycle-regulated genes of the yeast Saccharomyces cerevisiae by microarray hybridization.Mol Biol Cell19989843569
Cyclin overexpression2Cells arrested in G1 for CLN3 overexpression.Spellman PTSpellman PT, Sherlock G, Zhang MQ, Iyer VR, Anders K, Eisen MB, Brown PO, Botstein D, Futcher BComprehensive identification of cell cycle-regulated genes of the yeast Saccharomyces cerevisiae by microarray hybridization.Mol Biol Cell19989843569
Cell cycle, elutriation14Culture synchronized by elutriation and samples removed at several time points up to 6.5 h.Spellman PTSpellman PT, Sherlock G, Zhang MQ, Iyer VR, Anders K, Eisen MB, Brown PO, Botstein D, Futcher BComprehensive identification of cell cycle-regulated genes of the yeast Saccharomyces cerevisiae by microarray hybridization.Mol Biol Cell19989843569
Snf/Swi mutants (v1_2.2)2swi1, swi2 deletion mutantsSudarsanam PSudarsanam P, Iyer VR, Brown PO, Winston FWhole-genome expression analysis of snf/swi mutants of Saccharomyces cerevisiae.Proc Natl Acad Sci U S A200010725359
Snf/Swi mutants (384_F_v1.0)8snf2, swi1 deletion mutants grown in minimal or rich mediaSudarsanam PSudarsanam P, Iyer VR, Brown PO, Winston FWhole-genome expression analysis of snf/swi mutants of Saccharomyces cerevisiae.Proc Natl Acad Sci U S A200010725359
Nutrient limitation under aerobic and anaerobic conditions24Expression profiling of MATa CEN.PK113-7D chemostat cultures grown either aerobically or anaerobically in media limited for either glucose, nitrogen, phosphorous, or sulfur. Results provide insight into the interaction between oxygen and nutrient responsive pathways.Tai SLTai SL, Boer VM, Daran-Lapujade P, Walsh MC, de Winde JH, Daran JM, Pronk JTTwo-dimensional transcriptome analysis in chemostat cultures. Combinatorial effects of oxygen availability and macronutrient limitation in Saccharomyces cerevisiae.J Biol Chem200515496405
Ssl1 mutant for a subunit of TFIIH response to methyl methanesulfonate12Analysis of Ssl1 mutant for a subunit of TFIIH treated with methyl methanesulfonate (MMS). Ssl1 mutant contains C406A substitution and is sensitive to DNA damaging agents such as MMSTakagi YTakagi Y, Masuda CA, Chang WH, Komori H, Wang D, Hunter T, Joazeiro CA, Kornberg RDUbiquitin ligase activity of TFIIH and the transcriptional response to DNA damage.Mol Cell200515837426
Ume6 regulon (Ye6100subA)8wt, ume6 deletion diploids during vegetative growth in glucose and acetateWilliams RMWilliams RM, Primig M, Washburn BK, Winzeler EA, Bellis M, Sarrauste de Menthiere C, Davis RW, Esposito REThe Ume6 regulon coordinates metabolic and meiotic gene expression in yeast.Proc Natl Acad Sci U S A200212370439
Ume6 regulon (Ye6100subB)8wt, ume6 deletion diploids during vegetative growth in glucose and acetateWilliams RMWilliams RM, Primig M, Washburn BK, Winzeler EA, Bellis M, Sarrauste de Menthiere C, Davis RW, Esposito REThe Ume6 regulon coordinates metabolic and meiotic gene expression in yeast.Proc Natl Acad Sci U S A200212370439
Ume6 regulon (Ye6100subC)8wt, ume6 deletion diploids during vegetative growth in glucose and acetateWilliams RMWilliams RM, Primig M, Washburn BK, Winzeler EA, Bellis M, Sarrauste de Menthiere C, Davis RW, Esposito REThe Ume6 regulon coordinates metabolic and meiotic gene expression in yeast.Proc Natl Acad Sci U S A200212370439
Ume6 regulon (Ye6100subD)8wt, ume6 deletion diploids during vegetative growth in glucose and acetateWilliams RMWilliams RM, Primig M, Washburn BK, Winzeler EA, Bellis M, Sarrauste de Menthiere C, Davis RW, Esposito REThe Ume6 regulon coordinates metabolic and meiotic gene expression in yeast.Proc Natl Acad Sci U S A200212370439
Heat shock transcription factor 1 mutant response to heat stress4Analysis of a heat shock transcription factor 1 (HSF1) temperature sensitive mutant strain subjected to heat stress at 33 degrees C. HSF1 mutant contains an arginine to serine and a phenylalanine to serine substitution at residues 206 and 256 respectively. Results identify novel targets of HSF1.Yamamoto AYamamoto A, Mizukami Y, Sakurai HIdentification of a novel class of target genes and a novel type of binding sequence of heat shock transcription factor in Saccharomyces cerevisiae.J Biol Chem200515647283
Transcription factor deletions7Study expression effects of single transcription factor deletions.Yeang CHYeang CH, Mak HC, McCuine S, Workman C, Jaakkola T, Ideker TValidation and refinement of gene-regulatory pathways on a network of physical interactions.Genome Biol200515998451
Ca(2+) exposure24n Saccharomyces cerevisiae, the Ca(2+)/calmodulin-dependent protein phosphatase, calcineurin, is activated by specific environmental conditions, including exposure to Ca(2+) and Na(+), and induces gene expression by regulating the Crz1p/Tcn1p transcription factor. We used DNA microarrays to perform a comprehensive analysis of calcineurin/Crz1p-dependent gene expression following addition of Ca(2+) (200 mm) or Na(+) (0.8 m) to yeast.Yoshimoto HYoshimoto H, Saltsman K, Gasch AP, Li HX, Ogawa N, Botstein D, Brown PO, Cyert MSGenome-wide analysis of gene expression regulated by the calcineurin/Crz1p signaling pathway in Saccharomyces cerevisiae.J Biol Chem200212058033
Na(+) exposure16n Saccharomyces cerevisiae, the Ca(2+)/calmodulin-dependent protein phosphatase, calcineurin, is activated by specific environmental conditions, including exposure to Ca(2+) and Na(+), and induces gene expression by regulating the Crz1p/Tcn1p transcription factor. We used DNA microarrays to perform a comprehensive analysis of calcineurin/Crz1p-dependent gene expression following addition of Ca(2+) (200 mm) or Na(+) (0.8 m) to yeast.Yoshimoto HYoshimoto H, Saltsman K, Gasch AP, Li HX, Ogawa N, Botstein D, Brown PO, Cyert MSGenome-wide analysis of gene expression regulated by the calcineurin/Crz1p signaling pathway in Saccharomyces cerevisiae.J Biol Chem200212058033
Iron uptake4In the yeast Saccharomyces cerevisiae, uptake of iron is largely regulated by the transcription factor Aft1. cDNA microarrays were used to identify new iron and AFT1-regulated genes.Yun CWYun CW, Ferea T, Rashford J, Ardon O, Brown PO, Botstein D, Kaplan J, Philpott CCDesferrioxamine-mediated iron uptake in Saccharomyces cerevisiae. Evidence for two pathways of iron uptake.J Biol Chem200010744769
Trans-acting regulatory variation (dye swap)90Investigation of trans-acting regulatory variation using laboratory (BY) and wild (RM) strains and 86 F1 haploid cross segregantsYvert GYvert G, Brem RB, Whittle J, Akey JM, Foss E, Smith EN, Mackelprang R, Kruglyak LTrans-acting regulatory variation in Saccharomyces cerevisiae and the role of transcription factors.Nat Genet200312897782
Trans-acting regulatory variation90Investigation of trans-acting regulatory variation using laboratory (BY) and wild (RM) strains and 86 F1 haploid cross segregantsYvert GYvert G, Brem RB, Whittle J, Akey JM, Foss E, Smith EN, Mackelprang R, Kruglyak LTrans-acting regulatory variation in Saccharomyces cerevisiae and the role of transcription factors.Nat Genet200312897782
Pseudohyphal Growth26Wild-type or isogenic fkh1 fkh2 cells (GZ45-17a) were synchronized with -factor, released, and sampled through two cell cycles. Relative mRNA abundance was analysed by competitive microarray hybridization.Zhu GZhu G, Spellman PT, Volpe T, Brown PO, Botstein D, Davis TN, Futcher BTwo yeast forkhead genes regulate the cell cycle and pseudohyphal growth.Nature200010894548