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Links from GEO DataSets

Items: 20

1.

The intestinal microbiota programs DNA methylation to control tissue homeostasis and inflammation [RNA-seq]

(Submitter supplied) Although much research has been done on the diversity of gut microbiome, little is known about the way it influences intestinal homeostasis under normal and pathogenic conditions. Epigenetic mechanisms have recently been suggested as operating at the interface between the microbiota and the intestinal epithelium cells (IECs). Using genome-wide analyses, we discovered that exposure to microbiota induced both global DNA hypomethylation and localized changes at regulatory elements, which culminates in activation of a set of “early sentinel” response genes that play a role in maintaining gut homeostasis. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: TXT
Series
Accession:
GSE136840
ID:
200136840
2.

In vivo loss of TET2 and TET2 results in aberrant differentiation and homeostasis in the small intestine

(Submitter supplied) Although much research has been done on the diversity of the gut microbiome, little is known about how it influences intestinal homeostasis under normal and pathogenic conditions. Epigenetic mechanisms have recently been suggested to operate at the interface between the microbiota and the intestinal epithelium. We performed whole-genome bisulfite sequencing on conventionally raised and germ-free mice, and discovered that exposure to commensal microbiota induced localized DNA methylation changes at regulatory elements, which are TET2/3-dependent. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL21273
6 Samples
Download data: BEDGRAPH
Series
Accession:
GSE206169
ID:
200206169
3.

The intestinal microbiota programs DNA methylation to control tissue homeostasis and inflammation [ATAC-Seq]

(Submitter supplied) Although much research has been done on the diversity of gut microbiome, little is known about the way it influences intestinal homeostasis under normal and pathogenic conditions. Epigenetic mechanisms have recently been suggested as operating at the interface between the microbiota and the intestinal epithelium cells (IECs). Using genome-wide analyses, we discovered that exposure to microbiota induced both global DNA hypomethylation and localized changes at regulatory elements, which culminates in activation of a set of “early sentinel” response genes that play a role in maintaining gut homeostasis. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: TXT
Series
Accession:
GSE141458
ID:
200141458
4.

The intestinal microbiota programs DNA methylation to control tissue homeostasis and inflammation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL21273 GPL13112
32 Samples
Download data: BEDGRAPH, TXT
Series
Accession:
GSE137037
ID:
200137037
5.

The intestinal microbiota programs DNA methylation to control tissue homeostasis and inflammation [BiSulfite-seq]

(Submitter supplied) Although much research has been done on the diversity of gut microbiome, little is known about the way it influences intestinal homeostasis under normal and pathogenic conditions. Epigenetic mechanisms have recently been suggested as operating at the interface between the microbiota and the intestinal epithelium cells (IECs). Using genome-wide analyses, we discovered that exposure to microbiota induced both global DNA hypomethylation and localized changes at regulatory elements, which culminates in activation of a set of “early sentinel” response genes that play a role in maintaining gut homeostasis. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL13112
8 Samples
Download data: BEDGRAPH
Series
Accession:
GSE125978
ID:
200125978
6.

Transcriptome study of colon epithelial cells in Reg3a-transgenic mice

(Submitter supplied) The human C-type lectin Reg3a (HIP/PAP) is an antimicrobial peptide that kills Gram-positive bacteria. Reg3a preserves gut microbiota homeostasis, reinforces intestinal barrier function and thereby helps to fight induced colitis in mice. Transcriptomic data revealed an upregulation of numerous genes involved in the robustness of the intestinal barrier, and the biosynthesis pathway of mucin core 1 and 3 O-glycans.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
35 Samples
Download data: CEL
Series
Accession:
GSE64932
ID:
200064932
7.

Genes controlling the activation of natural killer lymphocytes are epigenetically remodeled in intestinal cells from germ-free mice

(Submitter supplied) Remodeling of the gut microbiota is implicated in various metabolic and inflammatory diseases of the gastrointestinal tract. We hypothesized that the gut microbiota affects the DNA methylation profile of intestinal epithelial cells (IECs) which could, in turn, alter intestinal function. Here, we used mass spectrometry and methylated DNA capture to respectively investigate global and genome-wide DNA methylation of intestinal epithelial cells from germ-free (GF) and conventionally raised mice (CONV-R). more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL17021
48 Samples
Download data: BED, CSV
Series
Accession:
GSE117434
ID:
200117434
8.

H3K27me3 analysis in mouse colonic epithelial cells

(Submitter supplied) H3K27me3 statuses were analyzed in normal mouse colonic epithelial cells and in those exposed to DSS-induced colitis, and aberrant changes of H3K27me3 by DSS-induced colitis were identified.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10324
3 Samples
Download data: TXT
Series
Accession:
GSE74007
ID:
200074007
9.

The epigenetic regulator Uhrf1 facilitates functional expansion of colonic regulatory T cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Methylation profiling by high throughput sequencing
Platforms:
GPL15103 GPL1261
12 Samples
Download data: CEL, WIG
Series
Accession:
GSE56544
ID:
200056544
10.

Genome-wide measuement of methylated cytosin in regulatory T cells (Treg) and conventional T cells (Tconv) depleted with Uhrf1

(Submitter supplied) To investigate the molecular mechanism how Uhrf1 regulate gene expression and cell cycle progression in Treg, we precipitated methylated DNA using recombinant MBD1 followed by genome-wide analysis of methylated gene loci by next generation sequencer
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL15103
4 Samples
Download data: WIG
Series
Accession:
GSE56543
ID:
200056543
11.

Expression data from CD4+ T cells of germ free mice, SPF IQI mice and SPF C57BL/6 mice depletd with Uhrf1 (by Cd4Cre-Uhrf1flox/flox)

(Submitter supplied) Commensal bacteria shapes gut immune system. Colonization bacteria increase the frequency of regulatory T cells, however, the molecular mechanisms has not yet been unknown. To reveal the mechanism, we isolated Treg cells and Non-Treg cells and performed the global expression analysis.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
8 Samples
Download data: CEL
Series
Accession:
GSE56542
ID:
200056542
12.

Metabolic products of an obesity-associated microbiome impact host metabolism and disease risk by altering the epigenome

(Submitter supplied) We profiled the gut microbiome and chromatin features at DNA cis-regulatory elements in colon epithelium from mice fed either an obesogenic or control diet.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL19057 GPL13112
84 Samples
Download data: BED, BIGWIG, TXT
Series
Accession:
GSE99670
ID:
200099670
13.

Metabolic products of an obesity-associated microbiome impact host metabolism and disease risk by altering the epigenome

(Submitter supplied) Mammals have a complicated symbiotic relationship with their gut microbiome which is postulated to have broad impacts on host health and disease. We used microarray to dectec the gene expressions in colon epithelium.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL20258
12 Samples
Download data: CEL
Series
Accession:
GSE99327
ID:
200099327
14.

VSL#3 supplementation of mice is associated primarily with changes in ileal microbiota composition and amelioration of DSS-induced colitis.

(Submitter supplied) Inflammatory bowel diseases encompass gastrointestinal illnesseses typified by chronic inflammation, loss of epithelial integrity and gastrointestinal microbiota dysbiosis. In an effort to counteract these characteristic perturbations, we used stem cells and/or a probiotic preparation in a murine model of Dextran Sodium Sulfate induced colitis to examine both their efficacy in ameliorating disease and impact on niche-specific microbial communities of the lower GI tract. more...
Organism:
Archaea; Mus musculus; Bacteria
Type:
Other
Platform:
GPL18000
94 Samples
Download data: CEL
Series
Accession:
GSE56137
ID:
200056137
15.

Hepatic gene expression co-regulated by diet-microbiota interactions (19 wk)

(Submitter supplied) Abstract: Histones are small proteins that form the core of nucleosomes, around which eukaryotic DNA wraps to ultimately form the highly organized and compressed structure known as chromatin. The N-terminal tails of histones are highly modified, and the modification state of these proteins dictates whether chromatin is permissive or repressive to processes that require physical access to DNA, including transcription and DNA replication and repair. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
15 Samples
Download data: TXT
Series
Accession:
GSE81117
ID:
200081117
16.

Hepatic gene expression co-regulated by diet-microbiota interactions (14 wk)

(Submitter supplied) Abstract: Histones are small proteins that form the core of nucleosomes, around which eukaryotic DNA wraps to ultimately form the highly organized and compressed structure known as chromatin. The N-terminal tails of histones are highly modified, and the modification state of these proteins dictates whether chromatin is permissive or repressive to processes that require physical access to DNA, including transcription and DNA replication and repair. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
9 Samples
Download data: TXT
Series
Accession:
GSE81115
ID:
200081115
17.

Genome-wide methylation analysis of AOM/DSS-induced colon tumors

(Submitter supplied) Genome-wide methylation analysis was performed by methylated DNA immunoprecipitation (MeDIP)-CpG island (CGI) microarray analysis to identify candidate CGIs specifically methylated in mouse colon tumors associated with colitis. We sucessfully identified 23 candidate CGIs methylated in tumors.
Organism:
Mus musculus
Type:
Methylation profiling by genome tiling array
Platform:
GPL10324
2 Samples
Download data: TXT
Series
Accession:
GSE21333
ID:
200021333
18.

The gut microbiome drives distinct methylome and transcriptome changes in intestinal epithelial cells during postnatal development

(Submitter supplied) We investigate the microbial effects on DNA methylation and the transcriptome of intestinal epithelial cells (IECs) during postnatal development
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL13112 GPL17021
59 Samples
Download data: TXT
Series
Accession:
GSE94402
ID:
200094402
19.

Comparison of murine colonic mucosal gene expression between postanatal day 90 (P90) to postnatal day 30 (P30)

(Submitter supplied) Comparison of murine colonic mucosal gene expression between postanatal day 90 (P90) to postnatal day 30 (P30) by whole genomic expression microarray. Gene expression profiling of colonic mucosal DNA between P90 and P30 mice. Agilent Technologies two-color labelling kit and genomic hybridization protocol was utilized.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
4 Samples
Download data: TXT
Series
Accession:
GSE19506
ID:
200019506
20.

Comparison of murine colonic mucosal DNA from postnatal day 90 (P90) to postnatal day 30 (P30) by MSAM

(Submitter supplied) DNA methylation profiling of colonic mucosal DNA between P90 and P30 mice. 0.5ug of DNA was serially digested with SmaI and XmaI followed by an adaptor ligation and adaptor mediated PCR amplification
Organism:
Mus musculus
Type:
Methylation profiling by genome tiling array
Platform:
GPL9158
2 Samples
Download data: TXT
Series
Accession:
GSE18031
ID:
200018031
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