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Links from GEO DataSets

Items: 15

1.

Gene expression in MEFs in response to treatment with dipyridyl and trichostatin A

(Submitter supplied) The CH1 protein interaction domain of the transcriptional coactivators p300 and CBP is thought to interact with HIF-1alpha and this interaction is thought to be critical to the expression of HIF-1alpha target genes in response to hypoxia. Trichostatin A (TSA), an inhibitor of histone deacetylases, has been reported to repress the expression of HIF-1alpha target genes. To test the requirement of the CH1 domain and TSA for gene expression in response to dipyridyl (a hypoxia mimetic), primary mouse embryonic fibroblasts (MEFs) were generated from C57Bl/6x129/Sv F2 e14.5 embryos that contain a deletion in the CH1 domain of three of four alleles of CBP and p300. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2162
Platform:
GPL1261
16 Samples
Download data
Series
Accession:
GSE3296
ID:
200003296
2.

Two transactivation mechanisms are responsible for the bulk of HIF-1alpha-responsive gene expression

(Submitter supplied) The C-terminal activation domain (C-TAD) of the hypoxia-inducible transcription factors HIF-1? and HIF-2? binds the CH1 domains of the related transcriptional coactivators CREB-binding protein (CBP) and p300, an oxygen-regulated interaction thought to be highly essential for hypoxia-responsive transcription. The role of the CH1 domain in vivo is unknown, however. We created mutant mice bearing deletions in the CH1 domains (?CH1) of CBP and p300 that abrogate their interactions with the C-TAD, revealing that the CH1 domains of CBP and p300 are genetically non-redundant and indispensable for C-TAD transactivation function. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL1261 GPL339
32 Samples
Download data
Series
Accession:
GSE3318
ID:
200003318
3.

Gene expression in hypoxic MEFs having only p300 and CBP with deleted CH1 domains

(Submitter supplied) The CH1 protein interaction domain of the transcriptional coactivators p300 and CBP is thought to interact with HIF-1alpha and this interaction is thought to be critical to the expression of HIF-1alpha target genes in response to hypoxia. To test the requirement of the CH1 domain for gene expression in response to hypoxia, rimary mouse embryonic fibroblasts (MEFs) were generated from C57Bl/6x129/Sv F2 e14.5 embryos that contain a deletion in the CH1 domain of three of four alleles of CBP and p300. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2161
Platform:
GPL1261
12 Samples
Download data
Series
Accession:
GSE3196
ID:
200003196
4.

Gene expression under normoxia/hypoxia in mouse embryonic fibroblasts with mutations in the CH1 domains of p300 and CBP

(Submitter supplied) The CH1 (TAZ) domain of the transcriptional coactivators p300 and CBP has been reported to interact with the transcription factor HIF-1alpha and this interaction is thought to be critical for HIF-1alpha target gene expression in response to hypoxia. To determine the requirement for the CH1 domain in hypoxia-responsive gene expression, primary mouse embryonic fibroblasts (MEFs) were generated from e14.5 C57B/6x129/Sv F2 embryos that were either wildtype or bore deletion mutations in the CH1 protein binding domains of both alleles of p300 and one allele of CBP (tri_CH1). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2160
Platform:
GPL339
4 Samples
Download data
Series
Accession:
GSE3195
ID:
200003195
5.
Full record GDS2162

CH1 domain deletion, p300 and CBP heterozygous null mutant hypoxic fibroblasts response to trichostatin A

Analysis of trichostatin A (TSA)-treated hypoxic fibroblasts with deletions in CH1 domains of p300 and CBP, and a p300 or CBP allele knockout. TSA is a histone deacetylase inhibitor. Results provide insight into the role of deacetylase activity in CH1-independent hypoxia inducible transcription.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 agent, 4 genotype/variation sets
Platform:
GPL1261
Series:
GSE3296
16 Samples
Download data
6.
Full record GDS2161

CH1 domain deletion, p300 and CBP heterozygous null mutant fibroblasts response to hypoxia

Analysis of hypoxic fibroblasts with deletions in the CH1 domains of p300 and CBP combined with a p300 or CBP allele knockout. CH1 domains interact with the C-TAD domain of hypoxia-inducible transcription factors HIF-1a and -2a. Results provide insight into the role for CH1 domains in hypoxia.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 genotype/variation, 2 stress sets
Platform:
GPL1261
Series:
GSE3196
12 Samples
Download data
7.
Full record GDS2160

CH1 domain deletions in p300 and CBP effect on hypoxic fibroblasts

Analysis of hypoxic fibroblasts bearing deletions in the CH1 domains of 1 allele of p300 and 2 alleles of CBP. CH1 domains interact with the C-TAD domain of hypoxia-inducible transcription factors HIF-1a and -2a. Results provide insight into the role of CH1 domains in the hypoxia response.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation, 2 stress sets
Platform:
GPL339
Series:
GSE3195
4 Samples
Download data
8.

Regulation of hypoxia-inducible factor activity by CHD4

(Submitter supplied) CHD4 coactivates a subset of HIF target genes in breast cancer MDA-MB-231 cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
8 Samples
Download data: TXT
9.

Genome-wide and single-cell analyses reveal target gene context-dependent relationship between Crebbp recruitment and both constitutive and signal-responsive gene expression.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL11002 GPL11180
20 Samples
Download data: BW, CEL
Series
Accession:
GSE54454
ID:
200054454
10.

CREBBP (CBP) ChIP-seq in wild type and CBP null MEFs +/- dipyridyl

(Submitter supplied) Genome-wide distribution of histone H3K18 and H3K27 acetyltransferases, Crebbp (CBP) and Ep300 (p300), is used to map enhancers and promoters, but whether these elements functionally require CBP/p300 remains largely uncertain. We investigated this relationship by comparing genomic CBP recruitment with gene expression in wild type and CBP/p300 double-knockout fibroblasts. ChIP-seq revealed nearby CBP recruitment for 20 percent of constitutively expressed genes, but surprisingly, three-quarters of these were unaffected or slightly activated by CBP/p300 deletion. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11002
8 Samples
Download data: BW
Series
Accession:
GSE54453
ID:
200054453
11.

Expression data from wild type and CBP/p300 null MEFs +/- 3hr treatment with 100uM dipyridyl (DP)

(Submitter supplied) Genome-wide distribution of histone H3K18 and H3K27 acetyltransferases, Crebbp (CBP) and Ep300 (p300), is used to map enhancers and promoters, but whether these elements functionally require CBP/p300 remains largely uncertain. We investigated this relationship by comparing genomic CBP recruitment with gene expression in wild type and CBP/p300 double-knockout fibroblasts. ChIP-seq revealed nearby CBP recruitment for 20 percent of constitutively expressed genes, but surprisingly, three-quarters of these were unaffected or slightly activated by CBP/p300 deletion. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
12 Samples
Download data: CEL
Series
Accession:
GSE54452
ID:
200054452
12.

The histone acetyl transferases CBP and p300 regulate stress response pathways in synovial fibroblasts

(Submitter supplied) The activation of stress response pathways in synovial fibroblasts (SF) is a hallmark of rheumatoid arthritis (RA). CBP and p300 are two highly homologous histone acetyl transferases and writers of activating histone 3 lysine 27 acetylation (H3K27ac) marks. We investigated individual functions of CBP and p300 using a silencing strategy, followed by RNA-sequencing, and pathway enrichment analysis. We have selected stress-related pathways for a further in-depth investigation of individual functions of CBP and p300 in SF. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
36 Samples
Download data: TXT
Series
Accession:
GSE236122
ID:
200236122
13.

Designed Oligooxopiperazines as Modulators of Hypoxia-Inducible Factor Signaling

(Submitter supplied) We performed gene expression profiling of oligooxopiperazines (OPs) targeting the hypoxia-inducible transcription factor complex. Treatment of cells with OPs inhibited hypoxia-inducible gene expression in A549 cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5067
Platform:
GPL6244
15 Samples
Download data: CEL
Series
Accession:
GSE48134
ID:
200048134
14.
Full record GDS5067

Oligooxopiperazine effect on hypoxic alveolar adenocarcinoma cell line

Analysis of hypoxic A549 cells treated with oligooxopiperazines (OOPs) BB2-125, BB2-162, and BB2-282. OOPs are designed mimics of a key α-helical domain at the interface of hypoxia-inducible factor 1α (HIF1α) and coactivator p300. Results provide insight into the effect of OOPs on HIF signaling.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 4 agent, 2 stress sets
Platform:
GPL6244
Series:
GSE48134
15 Samples
Download data: CEL
15.

Protein Domain Mimetics as In Vivo Modulators of Hypoxia-Inducible Factor Signaling

(Submitter supplied) We performed gene expression profiling of hydrogen-bond surrogate that targets hypoxia-inducible transcription factior complex and results in inhibition of hypoxia-inducible genes with relatively minimal perturbation of non-targeted signaling pathways.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
12 Samples
Download data: CEL
Series
Accession:
GSE48002
ID:
200048002
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Supplemental Content

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