U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 20

1.

The contribution of the post-transcriptional regulator CsrA to RNA stability and translation and identification of binding partners

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL15010
50 Samples
Download data
Series
Accession:
GSE102386
ID:
200102386
2.

The contribution of the post-transcriptional regulator CsrA to translation

(Submitter supplied) Analysis of the contribution of the post-transcriptional regulator CsrA to translation during exponential growth in Escherichia coli
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL15010
20 Samples
Download data: CSV
Series
Accession:
GSE102385
ID:
200102385
3.

The contribution of the post-transcriptional regulator CsrA to RNA stability

(Submitter supplied) Analysis of the contribution of the post-transcriptional regulator CsrA to RNA stability during exponential growth in Escherichia coli
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15010
20 Samples
Download data: CSV
Series
Accession:
GSE102381
ID:
200102381
4.

RNA binding partners of the post-transcriptional regulator CsrA

(Submitter supplied) Analysis of RNA binding partners of the post-transcriptional regulator CsrA to translation during exponential growth in Escherichia coli
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Other
Platform:
GPL15010
10 Samples
Download data: CSV
Series
Accession:
GSE102380
ID:
200102380
5.

Global maps of ProQ binding in vivo reveal target recognition via RNA structure and stability control at mRNA 3' ends

(Submitter supplied) In this study binding sites for the RNA-binding protein ProQ was determined in Salmonella and Escherichia coli
Organism:
Escherichia coli str. K-12 substr. MG1655; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344
Type:
Other
Platforms:
GPL21117 GPL20056
10 Samples
Download data: WIG
Series
Accession:
GSE106633
ID:
200106633
6.

The Legionella pneumophila genome evolved to accommodate multiple regulatory mechanisms controlled by the CsrA-system

(Submitter supplied) The RNA binding protein CsrA is the master regulator of the bi-phasic life cycle of Legionella pneumophila governing virulence expression in this intracellular pathogen. The goal of the study was to use deep sequencing of RNA enriched by co-immunoprecipitation with epitope tagged CsrA to identify CsrA-associated transcripts at the genome level. We found 478 mRNAs or non-coding RNAs to be targets of CsrA. more...
Organism:
Legionella pneumophila str. Paris
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL22984
10 Samples
Download data: WIG
Series
Accession:
GSE94068
ID:
200094068
7.

E. coli MazF does not create specialized ribosomes that translate leaderless mRNAs, but instead blocks rRNA maturation and ribosome biogenesis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Escherichia coli
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL14548 GPL21222
19 Samples
Download data
Series
Accession:
GSE107330
ID:
200107330
8.

E. coli MazF does not create specialized ribosomes that translate leaderless mRNAs, but instead blocks rRNA maturation and ribosome biogenesis [5'OH-seq]

(Submitter supplied) The purpose of this experiment was to characterize MazF cleavage specificity with single-nucleotide resolution by enriching and sequencing 5’-OH ends (a 5’-OH end is generated by MazF cleavage).
Organism:
Escherichia coli
Type:
Other
Platform:
GPL14548
2 Samples
Download data: CSV
Series
Accession:
GSE107329
ID:
200107329
9.

E. coli MazF does not create specialized ribosomes that translate leaderless mRNAs, but instead blocks rRNA maturation and ribosome biogenesis [Ribo-Seq]

(Submitter supplied) The purpose of this experiment was to assess translation of mRNA after MazF expression to determine if cleavage events resulted in a loss in ribosome footprints.
Organism:
Escherichia coli
Type:
Other
Platform:
GPL21222
3 Samples
Download data: CSV
Series
Accession:
GSE107328
ID:
200107328
10.

E. coli MazF does not create specialized ribosomes that translate leaderless mRNAs, but instead blocks rRNA maturation and ribosome biogenesis [RNA-seq]

(Submitter supplied) The purpose of this experiment was to characterize MazF cleavage specificity and locations of cleavage genome-wide in E. coli and also identify any leaderless transcripts .To do this, MazF was expressed in a ΔmazF background and compared to an empty vector. rRNA-subtracted samples were used to assess cleavage in the mRNA, and total RNA samples were used to assess changes in the rRNA.
Organism:
Escherichia coli
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21222
14 Samples
Download data: CSV
Series
Accession:
GSE107327
ID:
200107327
11.

Genomic Targets and Features of BarA-UvrY (-SirA) Signal Transduction Systems

(Submitter supplied) Using ChIP-exo, we have identified at single nucleotide resolution genomic binding sites for UvrY in E. coli and its homolog SirA in S. Typhimurium.
Organism:
Salmonella enterica subsp. enterica serovar Typhimurium str. 14028S; Escherichia coli str. K-12 substr. MG1655
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL15010 GPL20046
2 Samples
Download data: TXT
Series
Accession:
GSE74810
ID:
200074810
12.

Analysis of the contribution of the post-transcriptional regulator CsrA to RNA stability in Salmonella during growth in LB and mLPM media

(Submitter supplied) Analysis of the contribution of the post-transcriptional regulator CsrA to RNA stability in Salmonella during growth in LB and mLPM media
Organism:
Salmonella enterica subsp. enterica serovar Typhimurium
Type:
Other
Platform:
GPL17070
39 Samples
Download data: CSV
Series
Accession:
GSE107835
ID:
200107835
13.

Analysis of the contribution of the post-transcriptional regulator CsrA to translation during exponential growth in Escherichia coli

(Submitter supplied) Analysis of the contribution of the post-transcriptional regulator CsrA to translation during exponential growth in Escherichia coli
Organism:
Salmonella enterica subsp. enterica serovar Typhimurium
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL17070
32 Samples
Download data: CSV
Series
Accession:
GSE107834
ID:
200107834
14.

Global RNA recognition patterns of post‐transcriptional regulators Hfq and CsrA revealed by UV crosslinking in vivo

(Submitter supplied) The molecular roles of many RNA‐binding proteins in bacterial post‐transcriptional gene regulation are not well understood. Approaches combining in vivo UV crosslinking with RNA deep sequencing (CLIP‐seq) have begun to revolutionize the transcriptome‐wide mapping of eukaryotic RNA‐binding protein target sites. We have applied CLIP‐seq to chart the target landscape of two major bacterial post‐transcriptional regulators, Hfq and CsrA, in the model pathogen Salmonella Typhimurium. more...
Organism:
Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20056
12 Samples
Download data: WIG
Series
Accession:
GSE74425
ID:
200074425
15.

Grad-seq shines light on unrecognized RNA and protein complexes in the model bacterium Escherichia coli

(Submitter supplied) Stable protein complexes, including those formed with RNA, are major building blocks of every living cell. Escherichia coli has been the leading organism with respect to global bacterial protein-protein networks. However, there has been no global census of RNA/protein complexes in this model species of microbiology. Here, we performed Grad-seq to establish an RNA/protein complexome, reconstructing sedimentation profiles in a glycerol gradient for ~85% of all E. more...
Organism:
Escherichia coli
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21222
22 Samples
Download data: WIG
Series
Accession:
GSE152974
ID:
200152974
16.

Metabolome and transcriptome-wide effects of the carbon storage regulator A in enteropathogenic Escherichia coli.

(Submitter supplied) The carbon storage regulator A (CsrA) is a conserved swivel of a global regulatory system known to regulate central carbon pathways, biofilm formation, motility, and pathogenicity. The aim of this study was to characterize changes in major metabolic pathways induced by CsrA in the human enteropathogenic Escherichia coli (EPEC) strain E2348/69. The EPEC strain E2348/69 and a csrA deletion mutant were grown under virulence factor inducing conditions and characterized by a combined analysis of their metabolomes and transcriptomes. more...
Organism:
Escherichia coli
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18133
6 Samples
Download data: TAB, XLS
Series
Accession:
GSE103415
ID:
200103415
17.

Elucidation and validation of new targets of the global regulator PdhR in Escherichia coli

(Submitter supplied) The pyruvate dehydrogenase regulator protein (PdhR) of Escherichia coli acts as a transcriptional regulator in a pyruvate dependent manner to control central metabolic fluxes. However, the complete PdhR regulon has not yet been uncovered. To achieve an extended understanding of its gene regulation network, we combined large-scale network inference and experimental verification of results obtained by a systems biology approach.
Organism:
Escherichia coli str. K-12 substr. MG1655; Escherichia coli; Escherichia coli O157:H7 str. EDL933; Escherichia coli CFT073; Escherichia coli O157:H7 str. Sakai
Type:
Expression profiling by array
Platform:
GPL13359
24 Samples
Download data: TXT
Series
Accession:
GSE31333
ID:
200031333
18.

Interrogation of RNA-protein interaction dynamics in bacterial growth

(Submitter supplied) RNA-protein interactions are fundamental for bacterial homeostasis. However, we lack a system-wide understanding of their dynamics upon environmental perturbation. In this study, we have characterised the dynamics of 91% of the Escherichia coli proteome and the RNA-interaction properties of 271 RNA-binding proteins (RBPs) at different growth phases. We find that 68% of RBPs differentially bind RNA across growth phases and reveal novel RBP functions for proteins like the chaperone HtpG, a new tRNA-binding protein. more...
Organism:
Escherichia coli
Type:
Other
Platform:
GPL16085
8 Samples
Download data: BEDGRAPH
Series
Accession:
GSE235661
ID:
200235661
19.

Deconvoluting Independent Regulatory Signals in the Escherichia coli Transcriptome

(Submitter supplied) ChIPexo experiment was performed on E. coli K12 MG1655 with various supplements designed to activate transcriptional regulators
Organism:
Escherichia coli K-12
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24377
4 Samples
Download data: GFF
Series
Accession:
GSE122320
ID:
200122320
20.

Expression profiling of multiple Escherichia coli strains on glucose minimal media

(Submitter supplied) RNA sequencing was performed on multiple E. coli strains grown on glucose minimal media
Organism:
Escherichia coli
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16085
14 Samples
Download data: CSV
Series
Accession:
GSE122296
ID:
200122296
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=15|qty=11|blobid=MCID_672c35a9e0354754b5493ad2|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Support Center