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Links from GEO DataSets

Items: 17

1.

Transcriptional redirection of activated SKN-1/NRF2 abates the negative metabolic outcomes of a perceived pathogen infection

(Submitter supplied) Optimal health requires perpetual transcriptional fidelity of gene expression. SKN-1/NRF2 is a cytoprotective transcription factor in C. elegans that regulates the expression of cellular defenses during stress, including: nutrient deprivation, redox imbalance, and xenobiotic and pathogen exposure. Constitutive activation of SKN-1 results in pleiotropic outcomes, including shortened lifespan and protective redistribution of somatic fat to the germline. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13657
15 Samples
Download data: TXT
Series
Accession:
GSE123531
ID:
200123531
2.

TRX-1 Regulates SKN-1 Nuclear Localization Cell Non-Autonomously in Caenorhabditis elegans

(Submitter supplied) The Caenorhabditis elegans oxidative stress response transcription factor, SKN-1, is essential for the maintenance of redox homeostasis and is a functional ortholog of the Nrf family of transcription factors. The numerous levels of regulation that govern these transcription factors underscore their importance. Here, we add a thioredoxin, encoded by trx-1, to the expansive list of SKN-1 regulators. We report that loss of trx-1 promotes nuclear localization of intestinal SKN-1 in a redox-independent, cell non-autonomous fashion from the ASJ neurons. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13657
4 Samples
Download data: XLS
Series
Accession:
GSE77976
ID:
200077976
3.

RNA-seq analysis of germline stem cell removal and loss of SKN-1 in C. elegans

(Submitter supplied) In C. elegans, ablation of germline stem cells (GSCs) extends lifespan, but also increases fat accumulation and alters lipid metabolism, raising the intriguing question of how these effects might be related. Here we show that a lack of GSCs results in a broad transcriptional reprogramming, in which the conserved detoxification regulator SKN-1/Nrf increases stress resistance, proteasome activity, and longevity. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13657
12 Samples
Download data: CSV
Series
Accession:
GSE63075
ID:
200063075
4.

Stimulation of Host Immune Defenses by a Small Molecule Protects C. elegans from Bacterial Infection

(Submitter supplied) The nematode Caenorhabditis elegans offers currently untapped potential for carrying out high-throughput, live-animal screens of low molecular weight compound libraries to identify molecules that target a variety of cellular processes. We previously used a bacterial infection assay in C. elegans to identify 119 compounds that affect host-microbe interactions among 37,214 tested. We subsequently found that one of these small molecules, RPW-24, protects C. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Dataset:
GDS4243
Platform:
GPL200
6 Samples
Download data: CEL
Series
Accession:
GSE37266
ID:
200037266
5.
Full record GDS4243

Host immune response of bacterial infected nematode stimulated with small molecule

Analysis of bacterial infected C. elegans treated with 70 μM RPW-24 or DMSO. In a C.elegans-bacterial infection assay screening small molecules, RPW-24 was identified as a putative antimicrobial agent. Results provide insight into C. elegans conserved immune response to bacterial infection.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array, count, 2 agent sets
Platform:
GPL200
Series:
GSE37266
6 Samples
Download data: CEL
6.

C.elegans treated with control or elt-2 RNAi during adulthood and exposed to E. coli or P. aeruginosa

(Submitter supplied) Transcriptional profiling of adult C.elegans exposed to E.coli or to GFP-expressing P. aeruginosa (strain PA14). For P. aeruginosa exposure, worms were separated into 2 groups - fully colonized (green) or non-colonized (dark).
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL9458
14 Samples
Download data: GPR
Series
Accession:
GSE63846
ID:
200063846
7.

Muscleblind Splicing Factor Regulates Longevity Through p38 MAPK Signaling

(Submitter supplied) Muscleblind-like splicing regulators (MBNLs) are RNA-binding factors that have an important role in developmental processes. Dysfunction of these factors is a key contributor of different neuromuscular degenerative disorders, including Myotonic Dystrophy type 1 (DM1). Since DM1 is a multisystemic disease characterized by symptoms resembling accelerated aging, we asked which cellular processes do MBNLs regulate that make them necessary for normal lifespan. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19757
6 Samples
Download data: TXT
Series
Accession:
GSE146801
ID:
200146801
8.

Transcriptomic analysis of ddi-1(icb156) mutants in C. elegans

(Submitter supplied) We used RNA-seq to identify gene expression changes in C. elegans ddi-1(icb156) mutants
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22765
6 Samples
Download data: H5
Series
Accession:
GSE241087
ID:
200241087
9.

SKN-1-dependent oxidative stress response in C. elegans

(Submitter supplied) Oxidative stress may play a role in normal aging. SKN-1 is a transcription factor necessary for intestine development in Caenorhabditis elegans, which also regulates the response to oxidative stress post-embryonically. Using DNA microarrays, we found that oxidative stress induces the antioxidant response, the heat shock response, and detoxification genes, while the expression of genes involved in homeostasis, development, and reproduction were decreased. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL200
11 Samples
Download data: CEL
Series
Accession:
GSE9301
ID:
200009301
10.

Response of C. elegans immune pathway mutants to P. aeruginosa infection

(Submitter supplied) Synchronized C. elegans cultures of three geontypes -- wildype N2, daf-2(e1370) and sma-6(wk7) -- were prepared using standard techniques (http://cmgm.stanford.edu/~kimlab/index_methods.html). Live young adult worms were split between NG plates pre-seeded with the non-pathogenic E. coli strain OP50 or the Pseudomonas aeruginosa clinical isolate PA14 and incubated at 25C for 4 or 24 hours before harvesting. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
4 related Platforms
26 Samples
Download data: TXT
Series
Accession:
GSE13473
ID:
200013473
11.

Genes regulated by PMK-1 and DAF-16 in a daf-2(e1368) background.

(Submitter supplied) Analysis of genes differentially expressed between daf-2(e1368) and daf-2(e1368);pmk-1(km25) and between daf-2(e1368) and daf-2(e1368);daf-16(mgDf47). These studies identified genes upregulated by wild-type PMK-1 and wild-type DAF-16. Keywords: genetic modification
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Dataset:
GDS3253
Platform:
GPL200
9 Samples
Download data: CEL
Series
Accession:
GSE5801
ID:
200005801
12.

C. elegans gene expression in response to the pathogenic P. aeruginosa strain PA14.

(Submitter supplied) Analysis of differential gene expression in C. elegans adults exposed to three different bacteria: E. coli strain OP50, wild-type P. aeruginosa PA14 and gacA mutant PA14. Samples were analyzed at 4 hours and 8 hours after exposure to the different bacteria. These studies identified C. elegans genes induced by pathogen infection. Keywords: Time course, response to pathogen infection
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Dataset:
GDS3252
Platform:
GPL200
18 Samples
Download data: CEL
Series
Accession:
GSE5793
ID:
200005793
13.
Full record GDS3253

MAP kinase PMK-1 and transcription factor DAF-16 deletion mutants

Analysis of daf-2(e1368) loss-of-function mutant and daf-2(e1368);pmk-1(km25) and daf-2(e1368);daf-16(mgDf47) double mutants. PMK-1 and DAF-16 confer enhanced pathogen resistance on daf-2 mutants relative to wild-type. Results suggest DAF-16 and PMK-1 upregulate distinct genes to promote immunity.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array, count, 3 genotype/variation sets
Platform:
GPL200
Series:
GSE5801
9 Samples
Download data: CEL
14.
Full record GDS3252

Young adult response to Pseudomonas aeruginosa PA14: time course

Analysis of strain fer-15(b26);fem-1(hc17) young adults exposed for up to 8 hrs to pathogenic Pseudomonas aeruginosa strain PA14, less pathogenic PA14 mutant gacA, and E. coli strain OP50 (normal food source). Results provide insight into the molecular basis of the response to a bacterial pathogen.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array, count, 3 infection, 2 time sets
Platform:
GPL200
Series:
GSE5793
18 Samples
Download data: CEL
15.

NIPI-3 regulates the expression of C. elegans immune genes

(Submitter supplied) Many pathogens secrete toxins that target key host processes resulting in the activation of immune pathways. The secreted Pseudomonas aeruginosa toxin Exotoxin A (ToxA) disrupts intestinal protein synthesis which triggers the induction of a subset of P. aeruginosa-response genes in the nematode Caenorhabditis elegans. We found that losing one ToxA-induced C. elegans gene, the Tribbles pseudokinase ortholog nipi-3, results in hypersusceptibility to both P. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL200
9 Samples
Download data: CEL
Series
Accession:
GSE87052
ID:
200087052
16.

WDR-23 and SKN-1 Nrf2 coordinate with the BLI-3 dual oxidase in response to iodide-triggered oxidative stress

(Submitter supplied) Excess iodide could lead to larve arrest to C. elegans, we screened for mutants that can survive in excess iodide and identified gain-of-function mutations in skn-1 and loss-of-function mutations in wdr-23 and bli-3. Genetic study uncover that wdr-23(lf) can interact with bli-3 mutations in a manner different from skn-1(gf). Transcriptome studies suggest that excess iodide causes developmental arrest largely independent of changes in gene expression, and wdr-23(lf) could affect the expression of a subset of genes by a mechanism different from SKN-1 activation.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18245
18 Samples
Download data: XLS
Series
Accession:
GSE117222
ID:
200117222
17.

HIF-1 and SKN-1 Coordinate the Transcriptional Response to Hydrogen Sulfide in C. elegans

(Submitter supplied) Hydrogen sulfide (H2S) has dramatic physiological effects on animals that are associated with improved survival in changing conditions. C. elegans grown in H2S are long-lived and thermotolerant (1). To begin to identify mechanisms by which adaptation to H2S effects fundamental physiological functions, we have defined transcriptional changes associated with the response to H2S. Using microarray analysis we observe rapid changes in the abundance of specific mRNAs. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL11171
3 Samples
Download data: PAIR
Series
Accession:
GSE25199
ID:
200025199
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