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Links from GEO DataSets

Items: 8

1.
Full record GDS2427

Arginine regulon repression and derepression

Analysis of cells with the arginine (Arg) regulon fully or partially repressed, or derepressed. Genes of the Arg regulon are coordinately repressed by the Arg repressor (ArgR) in response to Arg. Results provide insight into ArgR-mediated repression of arginine biosynthesis and uptake genes.
Organism:
Escherichia coli
Type:
Expression profiling by array, count, 2 genotype/variation, 2 growth protocol, 3 other sets
Platform:
GPL3154
Series:
GSE4724
9 Samples
Download data: CEL, EXP
DataSet
Accession:
GDS2427
ID:
2427
2.

Transcriptome analysis of the arginine regulon in E.coli

(Submitter supplied) Analysis of the response to arginine of the Escherichia coli K-12 transcriptome by microarray hybridization and real-time quantitative PCR provides a first coherent quantitative picture of the ArgR-mediated repression of arginine biosynthesis and uptake genes. Transcriptional repression was shown to be the major control mechanism of the biosynthetic genes, leaving only limited room for additional transcriptional or post-transcriptional regulations. more...
Organism:
Escherichia coli
Type:
Expression profiling by array
Dataset:
GDS2427
Platform:
GPL3154
9 Samples
Download data: CEL, EXP
Series
Accession:
GSE4724
ID:
200004724
3.

Genome-scale reconstruction of the PurR regulon reveals its role in the adenine stimulon of Escherichia coli K-12 MG1655

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Escherichia coli str. K-12 substr. MG1655; Escherichia coli
Type:
Expression profiling by array; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL3154 GPL8387
12 Samples
Download data: CEL, PAIR
Series
Accession:
GSE26591
ID:
200026591
4.

ChIP-chip of E. coli K-12 MG1655 with antibody against PurR-8myc under various conditions.

(Submitter supplied) We integrated transcription factor binding regions and mRNA transcript abundance to elucidate the PurR regulon experimentally. To measure transcription factor binding at a genome scale, we employed a ChIP-chip method to derivative strains of E. coli K-12 MG1655 harboring PurR-8myc under various conditions.
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8387
4 Samples
Download data: PAIR
Series
Accession:
GSE26589
ID:
200026589
5.

Transcriptome analysis of E. coli MG1655

(Submitter supplied) Expression profiling of wild type and purR deletion strains of E. coli K-12 MG1655 under both M9 minimal media and addition of adenine.
Organism:
Escherichia coli; Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by array
Platform:
GPL3154
8 Samples
Download data: CEL
Series
Accession:
GSE26588
ID:
200026588
6.

In vivo probing of the DNA-binding Architecture by bacterial arginine repressor

(Submitter supplied) Although DNA motifs recognized by the transcription factors (TFs) have been determined, challenges remain in probing in vivo architecture of TF-DNA complexes on a genome-wide scale. Here, we show in vivo architecture of Escherichia coli arginine repressor (ArgR)-DNA complexes using chromatin immunoprecipitation coupled with sequencing (ChIP-exo). The identified 62 ArgR-binding loci were classified into three groups, comprised of single, double, and triple peak-pairs, respectively. more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17439
2 Samples
Download data: GFF
Series
Accession:
GSE60546
ID:
200060546
7.

S coelicolor ∆argR vs S. coelicolor M145

(Submitter supplied) S. coelicolor M145 and S. coelicolor ∆argR were grown in MG medium and samples from 3 biological replicates were taken at 32, 42, 49, 56 and 66 hours.
Organism:
Streptomyces coelicolor A3(2); Streptomyces coelicolor
Type:
Expression profiling by array
Platform:
GPL16698
30 Samples
Download data: TXT
Series
Accession:
GSE58666
ID:
200058666
8.

Response and adaptation to growth with low glucose concentration

(Submitter supplied) The faecal indicator bacterium Escherichia coli K12 was used to study the cellular events that take place at the transcription level using the microarray technology during short-term (physiological) and long-term (genetic) adaptation to slow growth under limited nutrient supply. Short-term and long-term adaptation were assessed by comparing the mRNA levels isolated after 40 or 500 hours of glucose-limited continuous culture at a dilution rate of 0.3 h-1 with those from batch culture with glucose excess. more...
Organism:
Escherichia coli; Escherichia coli K-12
Type:
Expression profiling by array
Platform:
GPL534
6 Samples
Download data
Series
Accession:
GSE4706
ID:
200004706
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Supplemental Content

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