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Links from GEO DataSets

Items: 20

1.

RNA Polymerase mapping during stress responses reveals widespread nonproductive transcription in yeast

(Submitter supplied) The use of genome-wide RNA abundance profiling by microarrays and deep sequencing has spurred a revolution in our understanding of transcriptional control. However, changes in mRNA abundance reflect the combined effect of changes in RNA production, processing, and degradation, and thus, mRNA levels provide an occluded view of transcriptional regulation. To partially disentangle these issues, we carry out genome-wide RNA Polymerase II (“Pol2”) localization profiling in budding yeast in two different stress response time courses. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by array
Platform:
GPL4131
18 Samples
Download data: GPR
Series
Accession:
GSE22675
ID:
200022675
2.

Control of chromatin structure by Spt6 has different consequences in coding and regulatory regions

(Submitter supplied) Spt6 is a highly conserved factor that carries out important functions in transcription and chromatin structure. To gain new insights into Spt6, we measured nucleosome occupancy along Saccharomyces cerevisiae chromosome III in an spt6 mutant and found that the level of nucleosomes is greatly reduced accross some but not all coding regions. In addition, genome-wide location analyses of RNA polymerase II showed that the nucleosome loss in the spt6 mutant occurs over highly-transcribed genes. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by array
Platform:
GPL4131
8 Samples
Download data: GPR, TIFF
Series
Accession:
GSE21787
ID:
200021787
3.

RNA pol II ChIP on chip (RPCC)

(Submitter supplied) Adaptation of the ChIP-on-chip protocol, to calculate genomic transcription rates in S. cerevisiae. Keywords: ChIP-chip
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platforms:
GPL6727 GPL7871
30 Samples
Download data
Series
Accession:
GSE14060
ID:
200014060
4.

Transcription rate analysis of wild type strain subjected to osmotic stress

(Submitter supplied) Transcription rate (TR) analysis of W303-1a yeast strain growing in exponential phase in YPD subjected to osmotic stress Keywords: time course
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL4565
35 Samples
Download data
Series
Accession:
GSE13096
ID:
200013096
5.

Gene Expression Kinetics

(Submitter supplied) We have taken five different time points of a Yeast culture in exponential grow in rich medium, each one elapsed ten minutes from de previous one (from OD600 0.36 to 0.47). Then, for each time point we have measured the transcription rates (TR) and mRNA amounts (RA) for all the genes using the Genomic run-on (GRO) technique .
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL6727
39 Samples
Download data
Series
Accession:
GSE11521
ID:
200011521
6.

Genomic Run-On (GRO) experiment for the YPD to YPGal time course

(Submitter supplied) Timecourse analyses (0 to 850 min) of exponentially growing BQS252 yeast after shift from YPD to YPGal galactose medium. Total RNA in vivo labeled by run-on, or cDNA labelling using random decamers included. Genomic DNA also examined. Keywords: other
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL772
42 Samples
Download data
Series
Accession:
GSE1002
ID:
200001002
7.

Transcriptomic study in RNA pol II foot mutants

(Submitter supplied) The goal of the project was to study the effects on transctiptome of some Rpb1 foot mutations that block Rpb4/7 assembly
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL8568
18 Samples
Download data: TXT
Series
Accession:
GSE65283
ID:
200065283
8.

Genomic Run On (GRO): determination of the nascent transcriptional rates and mRNA levels in several yeast mutants.

(Submitter supplied) In order to maintain the appropriate level of mRNA it is necessary coordinate simultaneously all the steps along the mRNA life cycle. It has been shown that several factors act in the regulation of gene expression as global coordinators. Thus, some kind of information is transferred from the nucleus to the cytoplasm, imprinted in the mRNA. In this way, it is conceivable the existence of mechanisms that ensure the balance between mRNA synthesis and degradation through the information flow from the cytoplasm to the nucleus and vice versa, as a crosstalk among both process to ensure the proper mRNA homeostasis in the cell. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL13620
18 Samples
Download data: TXT
Series
Accession:
GSE57467
ID:
200057467
9.

Hog1 bypasses stress-mediated down-regulation of transcription by PolII redistribution and chromatin remodeling

(Submitter supplied) Cells are subjected to dramatic changes on gene expression upon environmental changes. Stress causes a general down-regulation of gene expression together with the induction of a set of stress-responsive genes. Genome wide localisation studies showed major changes on Pol II localisation towards stress-responsive genes in contrast to housekeeping genes. Pol II relocalisation requires of the Hog1 SAPK, which also associates at stress-responsive loci. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13272
15 Samples
Download data: BED
Series
Accession:
GSE41494
ID:
200041494
10.

Hog1 bypasses stress-mediated downregulation of transcription by PolII redistribution and chromatin remodeling

(Submitter supplied) Hog1 bypasses stress-mediated downregulation of transcription by PolII redistribution and chromatin remodeling Keyword: genetic modification
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL7542
3 Samples
Download data: GPR
Series
Accession:
GSE41451
ID:
200041451
11.

Genome-wide analysis of mRNA lengths in Saccharomyces cerevisiae

(Submitter supplied) We developed a 'Virtual Northern' method, using DNA microarrays for genome-wide systematic analysis of mRNA lengths. We used this method to measure mRNAs corresponding to 84% of the annotated open reading frames (ORFs) in the S. cerevisiae genome, with high precision and accuracy (measurement errors 1 6-7%). We found a close linear relationship between mRNA lengths and the lengths of known or predicted translated sequences; mRNAs were typically around 300 nucleotides longer than the translated sequences. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL3292
35 Samples
Download data
Series
Accession:
GSE3932
ID:
200003932
12.

Global mRNA expression analysis in myo1 delta strains of the budding yeast Saccharomyces cerevisiae

(Submitter supplied) The Saccharomyces cerevisiae MYO1 gene encodes the myosin type II heavy chain (Myo1p), a protein required for normal cytokinesis in budding yeast. Deletion of the MYO1 gene prevents actomyosin-driven cytokinesis thereby activating an alternative mechanism that involves the synthesis of a remedial septum. Myo1p deficiency in yeast (myo1) also causes the formation of attached cells, abnormal budding patterns, formation of enlarged and elongated cells, increased osmotic sensitivity, delocalized chitin deposition, and increased chitin synthesis. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL884
6 Samples
Download data: TXT
Series
Accession:
GSE5931
ID:
200005931
13.

Genome-wide analysis of RNA polymerase II termination at protein-coding genes

(Submitter supplied) At the end of protein-coding genes, RNA polymerase (Pol) II undergoes a concerted transition that involves 3’-processing of the pre-mRNA and transcription termination. Here we conduct a genome-wide analysis of this 3’-transition in yeast. We find that the 3’-transition globally requires the Pol II elongation factor Spt5 and factors involved in the recognition of the poly-adenylation (pA) site and in endonucleolytic RNA cleavage. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18085 GPL17582 GPL13272
44 Samples
Download data: BED, TXT
Series
Accession:
GSE79222
ID:
200079222
14.

Pol II localization in yeast termination mutants

(Submitter supplied) RNA Polymerase II was mapped over 4% of the yeast genome by ChIP, in wild-type and a handful of mutants in transcriptional termination factors. Keywords: ChIP-chip, transcription termination
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL1950
9 Samples
Download data
Series
Accession:
GSE6301
ID:
200006301
15.

Nuclear RNA decay pathways aid rapid remodeling of gene expression in yeast

(Submitter supplied) In budding yeast, the nuclear RNA surveillance system is active on all pre-mRNA transcripts and modulated by nutrient availability. To test the role of nuclear surveillance in reprograming gene expression, we identified transcriptome-wide binding sites for RNA polymerase II (Pol II) and the exosome cofactors Mtr4 (TRAMP complex) and Nab3 (NNS complex) by UV-crosslinking immediately following glucose withdrawal (0, 4, and 8 minutes). more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL13821
24 Samples
Download data: BEDGRAPH, BW
Series
Accession:
GSE86483
ID:
200086483
16.

Affinity purification of ribosomes and associated RNAs from stress-treated cells using tagged Rpl16a and Rpl16b

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array; Other
Platforms:
GPL7662 GPL8546
60 Samples
Download data
Series
Accession:
GSE13682
ID:
200013682
17.

Affinity purification of ribosomes and associated RNAs using tagged Rpl16a and Rpl16b

(Submitter supplied) In this study, we systematically identified RNAs associated with ribosomes. To identify ribosome associated RNAs, C-terminal ZZ-tagged Rpl16a or Rpl16b, expressed under control of thier native promoter, were affinity purified from whole cell extracts of cultures grown to mid-log phase in minimal medium. Extracts were incubated with immunoglobulin G (IgG) coupled microbeads, washed, and ribosomes were eluted by tobacco etch virus (TEV) protease treatment. more...
Organism:
Saccharomyces cerevisiae
Type:
Other
Platform:
GPL8546
8 Samples
Download data
Series
Accession:
GSE13654
ID:
200013654
18.

Affinity purification of ribosomes and associated RNAs from stress-treated cells

(Submitter supplied) In this study, we systematically identified ribosome associated RNAs. To identify ribosome associated RNAs, C-terminal ZZ-tagged Rpl16a, expressed under control of its native promoter, was affinity purified from whole cell extracts of cultures grown to mid-log phase. Extracts were incubated with immunoglobulin G (IgG) coupled microbeads, washed, and ribosomes were eluted by tobacco etch virus (TEV) protease treatment. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array; Other
Platform:
GPL7662
52 Samples
Download data
Series
Accession:
GSE13653
ID:
200013653
19.

Budding yeast RNA polymerase II CTD phosphorylation and transcription termination factor localization

(Submitter supplied) Whole genome analysis of total RNA pol II, Ser2-, Ser5- and Ser7-phosphorylated RNA pol II, in WT and mutants of the C-terminal domain (CTD) kinases Ctk1 and Kin28, and localization of the termination factors Pcf11, Nrd1 and Rat1.
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL4613
12 Samples
Download data: GFF, PAIR, TXT
Series
Accession:
GSE23960
ID:
200023960
20.

Oxidative stress in stationary-phase cultures

(Submitter supplied) Background: As carbon sources are exhausted, Saccharomyces cerevisiae cells exhibit reduced metabolic activity and cultures enter stationary phase. We asked whether cells in stationary-phase cultures respond to additional stress at the level of transcript abundance. Results: Microarrays were used to quantify changes in transcript abundance in cells from stationary-phase cultures. In response to oxidative stress, more than 800 mRNAs increased within 1 minute. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platforms:
GPL1859 GPL3153
219 Samples
Download data: TIFF
Series
Accession:
GSE3729
ID:
200003729
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