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: 17

1.

The NtrYX two-component system regulates the bacterial cell envelope

(Submitter supplied) To investigate the R. sphaeroides NtrYX two component system on RNA transcript levels, we used global RNA sequencing (RNA-seq) to compare transcript abundance in parent and DntrYX strains grown under aerobic conditions. Our previous studies were performed in strains deficient at synthesizing the polyhydroxybutyrate, so we used strains D0382 and DNtrYXD0382, herein referred to as parent and DntrYX, respectively. more...
Organism:
Cereibacter sphaeroides 2.4.1
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18842 GPL28141
11 Samples
Download data: WIG, XLSX
Series
Accession:
GSE145442
ID:
200145442
2.

Defining the transcriptional regulon of ChvI in Caulobacter crescentus

(Submitter supplied) We sought to define the transcriptional regulon of the ChvI response regulator in Caulobacter crescentus. This study compares gene expression between ∆chvI cells and cells overexpressing the constitutively-active chvI(D52E) mutant. Our work provides a global view of the genes directly and indirectly regulated by the ChvGI two-component system in C. crescentus.
Organism:
Caulobacter vibrioides
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24555
12 Samples
Download data: TXT
Series
Accession:
GSE168965
ID:
200168965
3.

The Essential Rhodobacter sphaeroides RSP1056-RSP0847 (CenKR) Two-Component System Regulated Tol-Pal and Cell Envelope Biosynthesis

(Submitter supplied) To determine the regulon of RSP1056-RSP0847 TCS (response regulator with DNA-binding domains) we used ChIP-seq to determine the genomic occupancy of RSP0847 in strains with a hyperactive (RSP0847(D56E)), WT, and low activity (ΔRSP1056, RSP0847(D56A)) TCS. We then correlated cenR binding sites with changes in global gene expression between WT and strains with a hyperactive (RSP1056(D56E)) or low activity (ΔRSP1056, RSP0847(D56A)) TCS in RNA-seq experiments.
Organism:
Cereibacter sphaeroides 2.4.1
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL30898 GPL30899
53 Samples
Download data: TXT, WIG
Series
Accession:
GSE186600
ID:
200186600
4.

Growth-phase dependent gene regulation in the alpha-proteobacterium Rhodobacter sphaeroides

(Submitter supplied) Global transcriptome analyses at different stages of growth were applied to monitor growth phase-dependent gene expression in the alpha-proteobacterium Rhodobacter sphaeroides. Cultures with low aeration, which underwent strong changes in levels of dissolved oxygen during growth, were compared to aerated cultures, which showed little variation in levels of dissolved oxygen. Cells were in stationary phase for 12 h or for 57 h before dilution into fresh medium. more...
Organism:
Cereibacter sphaeroides 2.4.1
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17213
8 Samples
Download data: WIG
Series
Accession:
GSE71844
ID:
200071844
5.

IscR of Rhodobacter sphaeroides functions as repressor of genes for iron-sulphur metabolism and represents a new type of iron-sulphur binding protein

(Submitter supplied) Iron-sulphur (Fe-S) clusters are ensembles of iron and sulphide centres. They are found in all life forms and are important components of many enzymes involved in diverse cellular processes, including respiration, DNA synthesis or gene regulation. However, the increase in oxygen after the emergence of oxygenic photosynthesis created a threat to Fe–S proteins and, consequently, to the organisms relying on them. more...
Organism:
Cereibacter sphaeroides 2.4.1
Type:
Expression profiling by array
Platform:
GPL15457
2 Samples
Download data: TXT
Series
Accession:
GSE65537
ID:
200065537
6.

R. sphaeroides pRCcsR1-4 vs. R. sphaeroides 2.4.1 pRK415 (aerobic conditions)

(Submitter supplied) Transcriptional profiling of R. sphaeroides pRCcsR1-4 comparing to control R. sphaeroides 2.4.1 pRK415 under aerobic conditions
Organism:
Cereibacter sphaeroides; Cereibacter sphaeroides 2.4.1
Type:
Expression profiling by array
Platform:
GPL15457
2 Samples
Download data: TXT
Series
Accession:
GSE67145
ID:
200067145
7.

CceR and AkgR regulate of central carbon and energy metabolism in α-Proteobacteria

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Cereibacter sphaeroides 2.4.1; Cereibacter sphaeroides
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL162 GPL18840 GPL18841
13 Samples
Download data: CEL, WIG
Series
Accession:
GSE63450
ID:
200063450
8.

Genome-wide protein-DNA interaction analysis of CceR and AkgR transcription factors

(Submitter supplied) To gain a better understanding of the transcription factors that regulate central carbon metabolism in Rhodobacter sphaeroides ChIP-seq was used to determine the genome-wide binding locations of 2 transcription factors: CceR (RSP_1663) and AkgR (RSP_0981) both predicted to be involved in the regulation of of central carbon and energy metabolism.
Organism:
Cereibacter sphaeroides
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18841 GPL18840
4 Samples
Download data: WIG
Series
Accession:
GSE63449
ID:
200063449
9.

Microarray analysis of Rhodobacter sphaeroides CceR and AkgR deletion strains

(Submitter supplied) To gain a better understanding of the transcription factors that regulate central carbon metabolism in Rhodobacter sphaeroides global gene expression analysis was used to determine genes under the regulatory influence of 2 transcription factors: CcmR (RSP_1663) and AkgR (RSP_0981) both predicted to be involved in the regulation of central carbon and energy metabolism.
Organism:
Cereibacter sphaeroides 2.4.1; Cereibacter sphaeroides
Type:
Expression profiling by array
Platform:
GPL162
12 Samples
Download data: CEL
Series
Accession:
GSE63448
ID:
200063448
10.

Transcriptome response to nitrosative stress in Rhodobacter sphaeroides 2.4.1

(Submitter supplied) DNA microarray analysis was employed to investigate the transcriptome response to nitrosative stress in a non-denitrifying facultative photosynthetic bacterium Rhodobacter sphaeroides 2.4.1. We focused on the role played by a nitric oxide-response transcriptional regulator NnrR in the response. The transcriptome profiles of R. sphaeroides 2.4.1 and its nnrR mutant before and after exposure to nitrosating agents S-nitrosoglutathione (GSNO) or sodium nitroprusside (SNP) under semiaerobic conditions were analyzed.
Organism:
Cereibacter sphaeroides 2.4.1
Type:
Expression profiling by array
Platform:
GPL162
12 Samples
Download data: CEL
Series
Accession:
GSE33641
ID:
200033641
11.

Expression data from Burkholderia multivorans mucoid and nonmucoid isolates

(Submitter supplied) Burkholderia multivorans comprises opportunistic bacteria infecting hosts such as cystic fibrosis (CF) patients. Bcc long-term infection of CF patient airways has been associated with emergence of phenotypic variation including the mucoid-to-nonmucoid colony morphotype. Here we studied three Burkholderia multivorans clonal isolates (mucoid D2095 (BM11L), and nonmucoid D2214G and D2214P) and a laboratory nonmucoid variant (BM11L-nmv1) obtained under prolonged stationary phase. more...
Organism:
Burkholderia cenocepacia J2315; Burkholderia multivorans; Burkholderia multivorans ATCC 17616
Type:
Expression profiling by array
Platform:
GPL13356
12 Samples
Download data: CEL
Series
Accession:
GSE111467
ID:
200111467
12.

Regulation of hydrogen peroxide-dependent gene expression in Rhodobacter sphaeroides: Regulatory functions of OxyR

(Submitter supplied) Transcriptome profiling of Rhodobacter sphaeroides cells (WT and delta-oxyR mutant) grown in semiaerobic conditions, 7 and 30 min after addition of H2O2 up to 1 mM Keywords: time series
Organism:
Cereibacter sphaeroides 2.4.1; Cereibacter sphaeroides
Type:
Expression profiling by array
Dataset:
GDS1908
Platform:
GPL162
15 Samples
Download data
Series
Accession:
GSE2829
ID:
200002829
13.
Full record GDS1908

Hydrogen peroxide response: time course

Expression profiling of oxyR deletion mutant and wild type cells following treatment with 1 mM hydrogen peroxide. OxyR is a transcription factor that senses oxidative stress. Results provide insight into the mechanisms involved in oxidative stress tolerance.
Organism:
Rhodobacter sphaeroides; Rhodobacter sphaeroides 2.4.1
Type:
Expression profiling by array, count, 2 genotype/variation, 3 time sets
Platform:
GPL162
Series:
GSE2829
15 Samples
Download data
14.

Rhodobacter sphaeroides 2.4.1 pRKSorX144 versus pRK415 under singlet oxygen stress.

(Submitter supplied) To learn more about the function of SorX, we constructed an over-expression strain. For this purpose, the sorX gene together with its 28-bp upstream region was cloned into the over-expression vector pRK4352 and expressed in the R. sphaeroides wild-type 2.4.1 background. The corresponding strain consequently exhibits a SorX over-expression that is driven by the constitutive 16S rRNA (RSP_4352) promoter. more...
Organism:
Cereibacter sphaeroides 2.4.1
Type:
Expression profiling by array
Platform:
GPL15457
3 Samples
Download data: TXT
Series
Accession:
GSE79421
ID:
200079421
15.

A unique mode of cross regulation in a cell envelope stress signaling system

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Brucella ovis
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL33317
19 Samples
Download data
Series
Accession:
GSE229183
ID:
200229183
16.

A unique mode of cross regulation in a cell envelope stress signaling system [RNA-seq]

(Submitter supplied) A multi-layered structure known as the cell envelope separates the controlled interior of Gram-negative bacteria from a fluctuating physical and chemical environment. Transcription of genes that determine cell envelope structure and function is commonly controlled by a class of environmental regulators known as two-component signal transduction systems (TCS), which are comprised of 1) sensor histidine kinases and 2) response regulators. more...
Organism:
Brucella ovis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33317
9 Samples
Download data: XLSX
Series
Accession:
GSE229181
ID:
200229181
17.

A unique mode of cross regulation in a cell envelope stress signaling system [ChIP-seq]

(Submitter supplied) A multi-layered structure known as the cell envelope separates the controlled interior of Gram-negative bacteria from a fluctuating physical and chemical environment. Transcription of genes that determine cell envelope structure and function is commonly controlled by a class of environmental regulators known as two-component signal transduction systems (TCS), which are comprised of 1) sensor histidine kinases and 2) response regulators. more...
Organism:
Brucella ovis
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL33317
10 Samples
Download data: CSV
Series
Accession:
GSE229120
ID:
200229120
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=16|qty=8|blobid=MCID_66d7e9d217e8137d4092ebe6|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

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center