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Links from GEO DataSets

Items: 20

1.
Full record GDS4021

Rosiglitazone effect on PRDM16-deficient inguinal white adipose tissue: stromal-vascular cells

Analysis of SV cells isolated from PRDM16-depleted inguinal white adipose tissue (WAT) treated with rosiglitazone. Antidiabetic PPARγ ligand drugs, such as rosiglitazone, activate a browning of WAT. Results provide insight into molecular mechanisms underlying white-to-brown fat conversion.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 agent, 2 genotype/variation sets
Platform:
GPL8321
Series:
GSE35011
8 Samples
Download data: CEL
2.

PPARg agonists induce a white-to-brown fat conversion through stabilization of PRDM16 protein

(Submitter supplied) Brown adipose tissue dissipates energy through heat and functions as a defense against cold and obesity. PPARγ ligands have been shown to induce the browning of white adipocytes; however, the underlying mechanisms remain unclear. Here we show that PPARγ ligands require full agonism to induce a brown fat gene program preferentially in subcutaneous white adipose. These effects require expression of PRDM16, a factor that controls the development of classical brown fat. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4021
Platform:
GPL8321
8 Samples
Download data: CEL
Series
Accession:
GSE35011
ID:
200035011
3.

Adipose subtype-selective recruitment of TLE3 in thermogenic gene programs

(Submitter supplied) Transcriptional effectors of white adipocyte-selective gene expression have not been described. TLE3 is a white-selective cofactor that acts reciprocally with the brown-selective cofactor Prdm16 to specify lipid storage and thermogenic gene programs. When expressed at elevated levels in brown fat, TLE3 counters Prdm16, suppressing brown-selective genes and inducing white-selective genes, resulting in impaired fatty acid oxidation and thermogenesis. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17777
4 Samples
Download data: CEL
Series
Accession:
GSE51223
ID:
200051223
4.

Brown versus white tissue adipose selective genes

(Submitter supplied) The aim of this study was to identify genes expressed selectively in brown adipose tissue as compared to white adipose tissue from the same animals. This analysis provides a gene set that is brown and white adipose selective. Keywords: tissue comparison from mice
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2813
Platform:
GPL1261
6 Samples
Download data: CEL, CHP, DCP, TXT
Series
Accession:
GSE8044
ID:
200008044
5.
Full record GDS2813

Brown and white adipose tissues

Comparison of brown and white adipose tissues. Brown fat cells are specialized to dissipate energy and can counteract obesity. Results provide insight into the molecular mechanisms controlling brown fat cell determination.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 tissue sets
Platform:
GPL1261
Series:
GSE8044
6 Samples
Download data: CEL, CHP, DCP, TXT
6.

RNA-Seq of subcutaneous inguinal white fat of Hlx transgenic mice and littermate controls.

(Submitter supplied) RNA-Seq of subcutaneous inguinal white fat of Hlx transgenic mice and littermate controls.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: TXT
Series
Accession:
GSE78143
ID:
200078143
7.

Expression Profiles of miRNAs in brown fat of mice at room temperature and cold exposure (8C)

(Submitter supplied) microRNAs levels were measured in brown adipose tissue of male C57Bl6N mice that were kept at RT or during cold exposure (8°C) for 24 hrs. Several miRNAs including myomirs were identified to be regulated in response to cold.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL7732
8 Samples
Download data: TXT
Series
Accession:
GSE41306
ID:
200041306
8.

Expression data from multiple mouse adipose depots

(Submitter supplied) Comparing gene expression profiles of murine subcutaneous vs. visceral adipose tissue. Gene expression was analyzed in two subcutaneous depots (inguinal and axillary) and two visceral depots (epididymal and mesenteric) from male C57Bl/6 mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5654
Platform:
GPL8321
12 Samples
Download data: CEL
Series
Accession:
GSE53307
ID:
200053307
9.
Full record GDS5654

Subcutaneous and visceral adipose tissues

Analysis of adipose tissue from two subcutaneous depots (inguinal and axillary) and two visceral depots (epididymal and mesenteric) from age-matched, C57Bl/6 males. SubQ and VISC represent two broad categories of obesity. Results provide insight into fat depot-specific molecular profiles.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 other, 2 tissue sets
Platform:
GPL8321
Series:
GSE53307
12 Samples
Download data: CEL
10.

NFIA Controls the Brown Fat Gene Program by Co-Localizing with PPARgamma at Cell-Type-Specific Enhancers

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL17021 GPL16417 GPL11002
48 Samples
Download data: BIGWIG, TXT
Series
Accession:
GSE83764
ID:
200083764
11.

NFIA Controls the Brown Fat Gene Program by Co-Localizing with PPARgamma at Cell-Type-Specific Enhancers (RNA)

(Submitter supplied) Brown fat dissipates energy as heat and protects against obesity. Here, we identified nuclear factor I-A (NFIA) as a novel transcriptional regulator of brown fat by a genome-wide open chromatin analysis of murine brown and white fat followed by motif analysis of brown-fat-specific open chromatin regions. NFIA and the adipogenic master regulator, PPARγ, co-localize at the brown-fat-specific enhancers. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
24 Samples
Download data: TXT
Series
Accession:
GSE83762
ID:
200083762
12.

NFIA Controls the Brown Fat Gene Program by Co-Localizing with PPARgamma at Cell-Type-Specific Enhancers (chromatin)

(Submitter supplied) Brown fat dissipates energy as heat and protects against obesity. Here, we identified nuclear factor I-A (NFIA) as a novel transcriptional regulator of brown fat by a genome-wide open chromatin analysis of murine brown and white fat followed by motif analysis of brown-fat-specific open chromatin regions. NFIA and the adipogenic master regulator, PPARgamma, co-localize at the brown-fat-specific enhancers. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL11002 GPL16417 GPL17021
24 Samples
Download data: BEDGRAPH, BIGWIG
Series
Accession:
GSE83757
ID:
200083757
13.

Expression data from C2C12 myoblasts transduced with PRDM16 or vector

(Submitter supplied) PRDM16 is a 140 kDa transcriptional coregulatory protein. PRDM16 has been shown to function as a bi-directional switch in brown fat cell fate by stimulating the development of brown fat cells from myf-5 positive myoblastic precursors. We used microarrays to detail the global programme of gene expression underlying the myoblasts-brown fat conversion induced by PRDM16.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8321
6 Samples
Download data: CEL
Series
Accession:
GSE15895
ID:
200015895
14.

Expression data of differentiated adipocyte treated with small molecules

(Submitter supplied) To treat obesity and its related metabolism, small molecules can be used. To investigate the role of small molecules, butein, sulfuretin, and resveratrol were treated in differentiated adipocytes to find important regulators in adipocyte biology. Each small molecules have their own charactaristics on adipocyte biology, comparison of expression profiles among three small molecules can offer new insight in adipocyte biology.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
5 Samples
Download data: CEL
Series
Accession:
GSE76672
ID:
200076672
15.

Cistromic and epigenomic changes in Prdm16 knock-out brown adipose tissue

(Submitter supplied) Prdm16 is a transcription factor that drives a complete program of brown adipocyte differentiation, but the mechanism by which Prdm16 activates gene transcription remains unknown. Utilizing ChIP-seq teqhnique, we found that Prdm16 binds to chromatin at/near many brown fat-selective genes in BAT. Interestingly, Prdm16-deficiency dramatically reduced the binding of Med1 to Prdm16-target sites. Indeed, Prdm16 binds and recruits Med1 to BAT-enriched genes and the loss of Prdm16 caused a fundamental change in chromatin architecture at key BAT-selective genes and also reduced transcirptional activity. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL13112 GPL11002
11 Samples
Download data: BW
Series
Accession:
GSE63965
ID:
200063965
16.

Epigenome in brown and white adipose tissue

(Submitter supplied) PR (PRD1-BF1-RIZ1 homologous) domain-containing 16 (PRDM16) drives a brown fat differentiation program, but the mechanisms by which PRDM16 activates brown fat-selective genes have been unclear. Through chromatin immunoprecipitation (ChIP) followed by deep sequencing (ChIP-seq) analyses in brown adipose tissue (BAT), we reveal that PRDM16 binding is highly enriched at a broad set of brown fat-selective genes. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
8 Samples
Download data: BW
Series
Accession:
GSE63964
ID:
200063964
17.

Browning of White Adipose Tissue with Roscovitine Induces a Distinct Population of UCP1+ Adipocytes.

(Submitter supplied) Analysis of FACS sorted UCP1+ adipocytes shows that the mRNA signature of brite adipocytes is distinct from beige adipocytes, which arise through catecholamine signaling.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17791
16 Samples
Download data: CEL
Series
Accession:
GSE87191
ID:
200087191
18.

RNA-seq analysis of visceral fat Treg signature genes in aged WT and PPARg-2KR mice.

(Submitter supplied) We investigated PPARgamma deacetylation in regulating visceral fat Treg cell transcriptomes
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: CSV, TXT
Series
Accession:
GSE111833
ID:
200111833
19.

Remodeling of white fat during browning involves YBX1 to drive thermogenic commitment

(Submitter supplied) Effects of YBX1 activation in PPARγ-indcuded C3H/10T1/2-SAM pre-adipocytes on the transcriptome of cells during early differentation stages
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
51 Samples
Download data: TSV
Series
Accession:
GSE149083
ID:
200149083
20.

Prdm16 Knockout Brown Adipose Tissue

(Submitter supplied) Gene expression profile from brown adipose tissues of Prdm16 knockout and wile type mice. Prdm16 is a transcription factor that regulates the thermogenic gene program in brown and beige adipocytes. However, whether Prdm16 is required for the development or physiological function of brown adipose tissue (BAT) in vivo has been unclear. By analyzing mice that selectively lacked Prdm16 in the brown adipose lineage, we found that Prdm16 was dispensable for embryonic BAT development.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10333
8 Samples
Download data: TXT
Series
Accession:
GSE55080
ID:
200055080
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