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: 16

1.

Barcoded DNA sequencing (BarSeq) samples from passaging of Caulobacter crescentus in medium containing cheesecloth

(Submitter supplied) BarSeq experiment enriching for C. crescentus mutants that do not adhere to cheesecloth.
Organism:
Caulobacter vibrioides
Type:
Other
Platform:
GPL21015
30 Samples
Download data: TXT
Series
Accession:
GSE119738
ID:
200119738
2.

A cryptic transcription factor regulates Caulobacter crescentus adhesion

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caulobacter vibrioides CB15
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL32211
14 Samples
Download data
Series
Accession:
GSE201499
ID:
200201499
3.

A cryptic transcription factor regulates Caulobacter crescentus adhesion [RNA-seq]

(Submitter supplied) Alphaproteobacteria commonly produce a polar adhesin that is anchored to the exterior of the cell envelope. In Caulobacter crescentus, this adhesin enables permanent attachment to solid surfaces and is known as the holdfast. An ensemble of two-component signal transduction (TCS) proteins control C. crescentus holdfast biogenesis by indirectly regulating expression of HfiA, a potent holdfast inhibitor. more...
Organism:
Caulobacter vibrioides CB15
Type:
Expression profiling by high throughput sequencing
Platform:
GPL32211
8 Samples
Download data: CSV
Series
Accession:
GSE201498
ID:
200201498
4.

A cryptic transcription factor regulates Caulobacter crescentus adhesion [ChIP-seq]

(Submitter supplied) Alphaproteobacteria commonly produce a polar adhesin that is anchored to the exterior of the cell envelope. In Caulobacter crescentus, this adhesin enables permanent attachment to solid surfaces and is known as the holdfast. An ensemble of two-component signal transduction (TCS) proteins control C. crescentus holdfast biogenesis by indirectly regulating expression of HfiA, a potent holdfast inhibitor. more...
Organism:
Caulobacter vibrioides CB15
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL32211
6 Samples
Download data: TXT
Series
Accession:
GSE201497
ID:
200201497
5.

Defining genes in the Caulobacter crescentus SpdR regulon

(Submitter supplied) We measured steady-state transcript levels in 1) wild-type C. crescentus, 2) an spdR response regulator deletion strain (ΔspdR), and an spdR phosphomimic strain (SpdR(D64E))
Organism:
Caulobacter vibrioides
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22063
9 Samples
Download data: TXT
Series
Accession:
GSE125783
ID:
200125783
6.

XRE Transcription Factors in Caulobacter and φCbK Modulate Adhesion and Phage Viability

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caulobacter vibrioides CB15
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL32211
63 Samples
Download data
Series
Accession:
GSE241057
ID:
200241057
7.

XRE Transcription Factors in Caulobacter and φCbK Modulate Adhesion and Phage Viability [RNA-seq]

(Submitter supplied) During infection, transcriptional changes in both the phage and its host bacterium influence the outcome of infection. The xenobiotic response element (XRE) family of transcription factors (TFs), which are commonly encoded by bacteria and phages, regulate diverse aspects of bacterial cell physiology and can impact phage infection dynamics. Through a pangenome analysis of Caulobacter species isolated from soil and aquatic ecosystems, we uncovered an apparent radiation of an XRE TF gene cluster, several of which have established functions in the regulation of holdfast adhesin development and biofilm formation in C. more...
Organism:
Caulobacter vibrioides CB15
Type:
Expression profiling by high throughput sequencing
Platform:
GPL32211
33 Samples
Download data: CSV
Series
Accession:
GSE241056
ID:
200241056
8.

XRE Transcription Factors in Caulobacter and φCbK Modulate Adhesion and Phage Viability [ChIP-seq]

(Submitter supplied) During infection, transcriptional changes in both the phage and its host bacterium influence the outcome of infection. The xenobiotic response element (XRE) family of transcription factors (TFs), which are commonly encoded by bacteria and phages, regulate diverse aspects of bacterial cell physiology and can impact phage infection dynamics. Through a pangenome analysis of Caulobacter species isolated from soil and aquatic ecosystems, we uncovered an apparent radiation of an XRE TF gene cluster, several of which have established functions in the regulation of holdfast adhesin development and biofilm formation in C. more...
Organism:
Caulobacter vibrioides CB15
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL32211
30 Samples
Download data: TXT
Series
Accession:
GSE241053
ID:
200241053
9.

Comparison of Expression Profiles for Agrobacterium tumefaciens visR mutant to wild-type strain.

(Submitter supplied) Many bacteria colonize surfaces and transition to a sessile mode of growth. The plant pathogen Agrobacterium tumefaciens produces a unipolar polysaccharide (UPP) adhesin at single cell poles that contact surfaces. Here we report that elevated levels of the intracellular signal cyclic diguanosine monophosphate (c-di-GMP) lead to surface-contact-independent UPP production and a red colony phenotype due to production of UPP and the exopolysaccharide cellulose, when A. more...
Organism:
Agrobacterium tumefaciens
Type:
Expression profiling by array
Platform:
GPL18993
3 Samples
Download data: GPR, TXT
Series
Accession:
GSE60565
ID:
200060565
10.

Defining the role of the General Stress Response regulators, SigT and GsrN, in control of the hyperosmotic stress response in Caulobacter crescentus

(Submitter supplied) We report gene expression responses of Caulobacter crescentus to osmotic upshock (150 mM sucrose). The goal of this study is compare the transcriptional responses of wild type, sigT deletion, and gsrN overexpression (gsrN++) strains. The data provide a high resolution view of how two major regulators of the general stress response (sigT and gsrN) shape transcription upon shift to a hyperosmotic environment.
Organism:
Caulobacter vibrioides
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21015
31 Samples
Download data: TXT
Series
Accession:
GSE114971
ID:
200114971
11.

Caulobacter vibrioides CB15N mRNA expression in M2-Glucose Vs. M2-Inositol

(Submitter supplied) The purpose of this experiment was to examine the differential transcriptional profiles of Caulobacter CB15N grown in M2-Glucose versus M2-Inositol.
Organism:
Caulobacter vibrioides
Type:
Expression profiling by array
Platform:
GPL2749
2 Samples
Download data
Series
Accession:
GSE12414
ID:
200012414
12.

Ribosome Profiling Reveals Translational Control During the Caulobacter crescentus cell cycle

(Submitter supplied) The Caulobacter cell cycle includes sequential differentiation of the cell poles and an asymmetric cell division yielding distinct daughter cells. RNA-seq and ribosome profiling were used to measure global messenger RNA (mRNA) abundance and translation levels throughout the Caulobacter cell cycle revealing translational control in 51% of cell cycle-regulated genes. Ribosome profiling levels were temporally regulated for ten proteins encoding asymmetrically localized multi-protein assemblies that specify cell fate upon cell division, with five ORFs being regulated with a >2 fold contribution from the translation efficiency. more...
Organism:
Caulobacter vibrioides NA1000
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL18276
12 Samples
Download data: TXT
Series
Accession:
GSE68200
ID:
200068200
13.

The coding and noncoding architecture of the Caulobacter crescentus genome

(Submitter supplied) Caulobacter crescentus undergoes an asymmetric cell division controlled by a genetic circuit that cycles in space and time. We provide a universal strategy for defining the coding potential of bacterial genomes by applying ribosome profiling, RNA-seq, global 5’-RACE, and liquid chromatography coupled with tandem mass spectrometry (LC-MS) data to the 4-megabase C. crescentus genome. We mapped transcript units at single base-pair resolution using RNA-seq together with global 5’ RACE. more...
Organism:
Caulobacter vibrioides NA1000
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL18275 GPL18276
4 Samples
Download data: TXT
Series
Accession:
GSE54883
ID:
200054883
14.

Absolute measurements of mRNA translation in C. crescentus reveal important fitness costs of Vitamin B12 scavenging

(Submitter supplied) Ribosome profiling samples of C. crescentus grown in M2G to measure absolute levels of mRNA translation in M2G media.
Organism:
Caulobacter vibrioides
Type:
Other
Platform:
GPL21015
3 Samples
Download data: TXT
Series
Accession:
GSE126485
ID:
200126485
15.

Contact-dependent killing by Caulobacter crescentus via cell surface-associated, glycine zipper proteins

(Submitter supplied) Most bacteria are in fierce competition with other species for limited nutrients. Some bacteria can kill nearby cells by secreting bacteriocins, a diverse group of proteinaceous antimicrobials. However, bacteriocins are typically freely diffusible, and so of little value to planktonic cells in aqueous environments. Here, we identify an atypical two-protein bacteriocin in the gamma-proteobacterium Caulobacter crescentus that is retained on the surface of producer cells where it mediates cell contact-dependent killing. more...
Organism:
Caulobacter vibrioides
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21015
1 Sample
Download data: WIG
Series
Accession:
GSE96582
ID:
200096582
16.

Caulobacter strains ET163 and ET166 vs. CB15N (wild-type)

(Submitter supplied) The goal of this study was to compare the expression profiles of inversion strains ET163 and ET166 to that of wild-type. To this end we performed transcriptional profiling of Caulobacter crescentus swarmer cells from strains ET163, ET166, and CB15N (WT).
Organism:
Caulobacter vibrioides CB15; Caulobacter vibrioides
Type:
Expression profiling by array
Platform:
GPL14163
4 Samples
Download data: TXT
Series
Accession:
GSE31468
ID:
200031468
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=1|qty=5|blobid=MCID_6778d5fe7eb86f557f4aafff|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