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Links from GEO DataSets

Items: 14

1.

Alteration of gene expression in differentiating C2C12 cells upon inhibition of PCAF by embelin

(Submitter supplied) KAT2B (PCAF) belongs to GNAT family of lysine acetyltransferases (KAT), which specifically acetylates histone H3K9 residue and several nonhistone proteins. PCAF is also a transcription coactivator. Due to the lack of PCAF, KAT specific small molecule inhibitor, the exclusive role of the acetyltransferase activity of PCAF is not well understood. Here we report that a hydroxy benzoquinone class of natural compound, embelin, specifically inhibits H3Lys9 acetylation in mice and recombinant PCAF mediated acetylation with near complete specificity in vitro. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
12 Samples
Download data: TXT
Series
Accession:
GSE39827
ID:
200039827
2.

Alteration of gene expression in two cell lines upon inhibition of PCAF by embelin

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL6887 GPL6480
16 Samples
Download data: TXT
Series
Accession:
GSE39829
ID:
200039829
3.

Alteration of gene expression in HEK 293T cells upon inhibition of PCAF by embelin

(Submitter supplied) KAT2B (PCAF) belongs to GNAT family of lysine acetyltransferases (KAT), which specifically acetylates histone H3K9 residue and several nonhistone proteins. PCAF is also a transcription coactivator. Due to the lack of PCAF, KAT specific small molecule inhibitor, the exclusive role of the acetyltransferase activity of PCAF is not well understood. Here we report that a hydroxy benzoquinone class of natural compound, embelin, specifically inhibits H3Lys9 acetylation in mice and recombinant PCAF mediated acetylation with near complete specificity in vitro. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
4 Samples
Download data: TXT
Series
Accession:
GSE39828
ID:
200039828
4.

Cell cycle regulatory mechanisms in skeletal muscle cells

(Submitter supplied) Genome wide gene expression analysis in G9a knockdown myoblasts
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17543
8 Samples
Download data: TXT
Series
Accession:
GSE70039
ID:
200070039
5.

CBP/p300 transcriptome

(Submitter supplied) Comparison of CBP/p300 gene knock-out, bromodomain inhibitor, and acetyltransferase inhibitors Cmpd-R and A-485 in the same cell line (MEF).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21163
25 Samples
Download data: TXT
Series
Accession:
GSE92613
ID:
200092613
6.

ChIP-seq profiling of transcriptional co-activator p300 during early myogenic differentiation

(Submitter supplied) Molecular regulation of stem cell differentiation is exerted through both genetic and epigenetic determinants over distal regulatory or enhancer regions. Understanding the mechanistic action of active or poised enhancers is thus imperative for control of stem cell differentiation. Based on a genome-wide co-occurrence of different epigenetic marks in committed proliferating myoblasts, we have previously generated a 14-state chromatin state model to profile residue-specific histone acetylation in early myoblast differentiation. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
3 Samples
Download data: BIGWIG, BW
Series
Accession:
GSE109636
ID:
200109636
7.

Gcn5 and PCAF negatively regulate interferon β production through HAT-independent inhibition of TBK1

(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
Platform:
GPL13112
9 Samples
Download data: TXT, WIG
Series
Accession:
GSE60969
ID:
200060969
8.

Gcn5 and PCAF negatively regulate interferon β production through HAT-independent inhibition of TBK1 [RNA-Seq]

(Submitter supplied) Gcn5/PCAF double knockout (dKO) leads to loss of the global H3K9ac. RNA-Seq was performed to define the changes of gene expression in response to Gcn5/PCAF deletion and H3K9ac loss
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
5 Samples
Download data: TXT
Series
Accession:
GSE60968
ID:
200060968
9.

Gcn5 and PCAF negatively regulate interferon β production through HAT-independent inhibition of TBK1 [ChIP-Seq]

(Submitter supplied) Gcn5/PCAF dobule knockout (dKO) in MEFs leads to loss of the global H3K9ac, but only affect expression of a small nubmer of genes according to RNA-Seq data. To examine the function of H3K9ac on gene activation, H3K9ac ChIP-Seq was performed. We found that H3K9ac at Transcriptional Start sites (TSSs) of no-changed, up-regulated and down-regulated genes are all dramatially decreased in Gcn5/PCAF dKO cells, suggesting that H3K9ac is largely not required for gene activation.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: TXT, WIG
Series
Accession:
GSE60967
ID:
200060967
10.

p300-mediated gene expression during muscle cell survival

(Submitter supplied) Type of experiment: The primary focus of these studies is to define the transcriptional network regulated by ectopic expression of the transcriptional co-activator protein, p300, in order to define its mechanism(s) of action in promoting muscle cell survival. Experimental factors: Our laboratory has generated a murine C2-derived myoblast cell line stably expressing an IGF-II cDNA in antisense orientation (C2AS12 cells). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS1821
Platform:
GPL81
6 Samples
Download data: PDF
Series
Accession:
GSE4224
ID:
200004224
11.
Full record GDS1821

Muscle cell survival mediated by transcriptional coactivator p300

Analysis of insulin growth factor II deficient C2AS12 myoblasts expressing wild type or protein interaction domain mutant p300 at 0 and 24 hours after a switch to low serum media. Wild type but not the mutant p300 prevents the progressive cell death induced by serum withdrawal.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 agent, 2 genotype/variation, 2 time sets
Platform:
GPL81
Series:
GSE4224
6 Samples
Download data
DataSet
Accession:
GDS1821
ID:
1821
12.

Distribution of p27- and PCAF binding sites (BS) on the chromatin of HCT116 cell line

(Submitter supplied) We analyzed the transcriptional programs regulated by PCAF and p27 in the colon cancer cell line HCT116 by ChIP-seq. We identified 269 protein-encoding genes that contain both p27 and PCAF binding sites being the majority of these sites different for PCAF and p27
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
4 Samples
Download data: WIG
Series
Accession:
GSE93975
ID:
200093975
13.

MeDIP-chip from dorsal root ganglia (DRG) tissue from wildtype mice, for 5-methyl-cytosine

(Submitter supplied) Nerve injury in the peripheral nervous system allows spontaneous regeneration, in contrast to injury of central nerves, which lead to a differential expression pattern of regeneration-associated genes and others. These genes might be regulated by promoter DNA methylation As regeneration model, DRG tissue was analyzed for methyated gene promoters and CpG islands following both injury types. A differential methylation pattern could be identified, although most genes remained unmethylated.
Organism:
Mus musculus
Type:
Methylation profiling by genome tiling array
Platform:
GPL18360
33 Samples
Download data: PAIR, TXT, XLS
Series
Accession:
GSE55514
ID:
200055514
14.

Sodium arsenite exposure inhibits histone acetyltransferase p300 for attenuating H3K27ac at enhancers in mouse embryonic fibroblast cells

(Submitter supplied) Both epidemiological investigations and animal studies have linked arsenic-contaminated water to cancers, in- cluding skin, liver and lung cancers. Besides genotoxicity, arsenic exposure-related pathogenesis of disease is widely considered through epigenetic mechanisms; however, the underlying mechanism remains to be deter- mined. Herein we explore the initial epigenetic changes via acute sodium arsenite (As) exposures of mouse em- bryonic fibroblast (MEF) cells and histone H3K79 methyltransferase Dot1L knockout (Dot1L−⁠ /−) MEF cells. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21273
6 Samples
Download data: BW, TXT
Series
Accession:
GSE118827
ID:
200118827
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