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Links from GEO DataSets

Items: 17

1.

RfaH counter-silences inhibition of transcript elongation by H-NS–StpA H-NS nucleoprotein filaments in pathogenic E. coli

(Submitter supplied) Expression of virulence genes in pathogenic E. coli is controlled in part by the transcription silencer H-NS and its paralogs (e.g., StpA), which sequester DNA in multi-kb nucleoprotein filaments to inhibit transcription initiation, elongation, or both. Some activators counter-silence initiation by displacing H-NS from promoters. How H-NS inhibition of elongation is overcome is not understood. In uropathogenic E. more...
Organism:
Escherichia coli CFT073; Escherichia coli
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL32598 GPL16085
97 Samples
Download data: BW
Series
Accession:
GSE212064
ID:
200212064
2.

Transcriptome-wide effects of NusA on RNA polymerase pausing in Bacillus subtilis

(Submitter supplied) In this work we conducted RNET-seq on Wild Type, NusA depletion, nusG deletion, and NusA depletion nusG deletion strains of B. subtilis. Using this data we analysed the transcriptome-wide effects of NusA on RNA polymerase pausing and found that NusA has modest pause stimulating as well as suppressing effects throughout the genome.
Organism:
Bacillus subtilis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18561
8 Samples
Download data: BW
Series
Accession:
GSE186285
ID:
200186285
3.

Role of stpA in Salmonella typhimurium

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; Salmonella enterica
Type:
Expression profiling by array; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL9091 GPL5780
40 Samples
Download data: GPR, TXT
Series
Accession:
GSE18452
ID:
200018452
4.

Identification of StpA-binding sites on the Salmonella genome

(Submitter supplied) We used ChIP-chip analysis to identify where the nucleoid associated protein StpA binds on the Salmonella Typhimurium genome. We identified 285 chromosomal regions bound by StpA, ranging in size from 400 to 3500 base pairs and containing 572 genes. Comparison of the ChIP data revealed that StpA displayed an identical binding profile to H-NS; all genomic regions associated with StpA were also bound by H-NS. more...
Organism:
Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; Salmonella enterica subsp. enterica serovar Typhimurium
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL5791
8 Samples
Download data: TXT
Series
Accession:
GSE18450
ID:
200018450
5.

StpA prevents RpoS-dependent transcription during mid-exponential growth in S. Typhimurium

(Submitter supplied) StpA is a paralogue of the nucleoid associated protein H-NS that is conserved in a range of enteric bacteria and had no known function in Salmonella enterica serovar Typhimurium. Here, we show that 5% of the Salmonella genome is regulated by StpA, which contrasts with the situation in Escherichia coli where deletion of stpA only had minor effects on gene expression. The StpA-dependent genes of S. Typhimurium are a specific subset of the H-NS regulon that are predominantly under the positive control of sigma38 (RpoS), CRP-cAMP and PhoP. more...
Organism:
Salmonella enterica; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344
Type:
Expression profiling by array
Platform:
GPL9091
12 Samples
Download data: GPR
Series
Accession:
GSE18428
ID:
200018428
6.

The effect of stpA deletion on S. Typhimurium gene expression during growth in rich medium

(Submitter supplied) StpA is a paralogue of the nucleoid associated protein H-NS that is conserved in a range of enteric bacteria and had no known function in Salmonella enterica serovar Typhimurium. Here, we show that 5% of the Salmonella genome is regulated by StpA, which contrasts with the situation in Escherichia coli where deletion of stpA only had minor effects on gene expression. The StpA-dependent genes of S. Typhimurium are a specific subset of the H-NS regulon that are predominantly under the positive control of sigma38 (RpoS), CRP-cAMP and PhoP. more...
Organism:
Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; Salmonella enterica
Type:
Expression profiling by array
Platforms:
GPL5780 GPL9091
28 Samples
Download data: GPR, TXT
Series
Accession:
GSE18424
ID:
200018424
7.

Global H-NS counter-silencing by LuxR activates quorum sensing gene expression [RNA-seq]

(Submitter supplied) Bacteria coordinate cellular behaviors using a cell-cell communication system termed quorum sensing. In Vibrio harveyi, the master quorum sensing transcriptional factor LuxR directly regulates >100 genes in response to changes in population density. Here, we show that LuxR derepresses quorum sensing loci by competing with H-NS, a global transcriptional repressor that oligomerizes on DNA to form filaments and bridges. more...
Organism:
Vibrio campbellii
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27117
12 Samples
Download data: TXT
Series
Accession:
GSE136191
ID:
200136191
8.

Global H-NS counter-silencing by LuxR activates quorum sensing gene expression

(Submitter supplied) Bacteria coordinate cellular behaviors using a cell-cell communication system termed quorum sensing. In Vibrio harveyi, the master quorum sensing transcriptional factor LuxR directly regulates >100 genes in response to changes in population density. Here, we show that LuxR derepresses quorum sensing loci by competing with H-NS, a global transcriptional repressor that oligomerizes on DNA to form filaments and bridges. more...
Organism:
Vibrio campbellii
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL27117
5 Samples
Download data: TXT
Series
Accession:
GSE136050
ID:
200136050
9.

Genomic analysis of the combined effects of H-NS and co-regulators on E. coli gene expression

(Submitter supplied) This entry refers to transcriptome analysis of E. coli with single deletions of hns, stpA, hha and ydgT and double deletions of hns with each of the other three regulators mentioned.
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15982
16 Samples
Download data: TXT
Series
Accession:
GSE40313
ID:
200040313
10.

Regulator trafficking on bacterial transcription units in vivo

(Submitter supplied) The in vivo trafficking patterns on DNA by the bacterial regulators of transcript elongation Sigma70, Rho, NusA, and NusG and the explanation for high promoter-proximal levels or peaks of RNA polymerase (RNAP) are unknown. Genome-wide ChIP-chip on E. coli revealed distinct association patterns of regulators as RNAP transcribes away from promoters (Rho first, then NusA, and then NusG). However, the interactions of elongating complexes with these regulators, including a weak interaction with Sigma70, did not differ significantly among most transcription units. more...
Organism:
Escherichia coli
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7790
17 Samples
Download data: TXT
Series
Accession:
GSE13938
ID:
200013938
11.

Overexpression of BglJ and LeuO in Escherichia coli K12

(Submitter supplied) The only target locus of transcription factor BglJ known to date is the bgl operon, and activation of bgl by BglJ requires RcsB. Transcription factor LeuO is involved in stress responses and known as antagonist of H-NS. To identifiy novel targets of BglJ, we overexpressed BglJ in Escherichia coli K12 and measured differential gene expression by performing DNA microarray analysis. Moreover, to analyze whether all targets of BglJ require RcsB, we overexpressed BglJ in an rcsB deletion background. more...
Organism:
Escherichia coli; Escherichia coli K-12
Type:
Expression profiling by array
Platform:
GPL3154
28 Samples
Download data: CEL
Series
Accession:
GSE34023
ID:
200034023
12.

Genome-wide assessments of transcriptional pauses and errors by nascent transcript sequencing combined with RNase footprinting (RNET-seq)

(Submitter supplied) We developed native elongating transcript sequencing (NET-seq, Churchman and Weissman Nature 2011, PMID: 21248844) combined with RNase footprinting of nascent transcripts (RNET-seq) to visualize translocation dynamics and nascent transcript errors in paused RNA polymerases in E. coli. We employed RNET-seq to the wild-type (WT) E. coli strain and to an isogenic strain deficient in genes for GreA and GreB (ΔgreAB). more...
Organism:
Escherichia coli
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18945
2 Samples
Download data: CSV
Series
Accession:
GSE62102
ID:
200062102
13.

Brucella MucR acts as an H-NS-like protein to silence virulence genes and structure the nucleoid 

(Submitter supplied) Histone-like nucleoid structuring (H-NS) and H-NS-like proteins serve as global gene silencers and work with antagonistic transcriptional activators (counter- silencers) to properly coordinate the expression of virulence genes in pathogenic bacteria. In Brucella, MucR has been proposed as a novel H-NS-like gene silencer, but direct experimental evidence is lacking. Here, we show that MucR serves as an H-NS-like silencer of the Brucella abortus genes encoding the polar autotransporter adhesins BtaE and BmaC, the c-di-GMP-specific phosphodiesterase BpdB, and the quorum-sensing regulator BabR. more...
Organism:
Brucella abortus 2308
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
Platform:
GPL33491
12 Samples
Download data: CSV, TXT
Series
Accession:
GSE234935
ID:
200234935
14.

The environmentally-regulated interplay between three-dimensional chromatin organisation and transcription of the Escherichia coli proVWX operon

(Submitter supplied) Nucleoid associated proteins maintain the architecture of bacterial chromosomes and regulate gene expression. Thus, their role as transcription factors may involve three-dimensional chromosome re-modelling. Here, we provide the first in vivo evidence supporting this hypothesis. Using RT-qPCR and 3C-qPCR, we show that activation of the H-NS-regulated, osmosensitive proVWX operon of Escherichia coli in response to a hyperosmotic shock involves the destabilization of H-NS-mediated bridges anchored between the proVWX downstream and upstream regulatory elements (DRE and URE), and between the DRE and ygaY that lies immediately downstream of proVWX. more...
Organism:
Escherichia coli str. K-12 substr. MG1655
Type:
Other
Platform:
GPL21117
11 Samples
Download data: HIC, PNG, TXT
Series
Accession:
GSE214511
ID:
200214511
15.

Transcriptomic study of single mutants hns, hns2 and double mutans hhahha2 and hnshns2 from enteroaggregative E. coli 042 by RNA-seq

(Submitter supplied) Bacterial genomes encode in many instances more than one copy of genes coding for global modulators. In the Enterobacteriaceae, cells express the global modulator H-NS and its paralogue StpA. The enteroaggregative E. coli strain 042 encodes, in addition to the hns and stpA genes, an additional hns gene. We used RNA-seq to compare the transcriptome of the wt strain and its hns, hns2 and double hns hns2 derivatives, as well as of an hha null mutant (hhahha2). more...
Organism:
Escherichia coli 042
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24145
5 Samples
Download data: XLS
Series
Accession:
GSE105133
ID:
200105133
16.

Characterization of Bacterial Transcriptional Regulatory Networks in Escherichia coli through Genome-Wide In Vitro Run-Off Transcription/RNA-seq (ROSE)

(Submitter supplied) The global characterization of transcriptional regulatory networks almost exclusively uses in vivo conditions, thereby providing a snapshot on multiple regulatory interactions at the same time. To complement these approaches, we developed and applied a method for characterizing bacterial promoters genome-wide by in vitro transcription coupled to transcriptome sequencing specific for native 5'-ends of transcripts. more...
Organism:
Escherichia coli
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL16085
10 Samples
Download data: BEDGRAPH, XLS
Series
Accession:
GSE159312
ID:
200159312
17.

Global timeospatial map of RNA polymerase in Escherichia coli

(Submitter supplied) To investigate the relationship between RNA polymerase binding and transcription ChIP-seq on the common house-keeping SigmaD and RNA polymerase beta subunit were coupled with RNA-seq at various growth phases of Escherichia coli in rich media.
Organism:
Escherichia coli
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL21433
40 Samples
Download data: BED, TXT
Series
Accession:
GSE153815
ID:
200153815
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