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Links from GEO DataSets

Items: 20

1.

The Aurora B kinase and the polycomb protein Ring1B combine to regulate active promoters in quiescent lymphocytes

(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
22 Samples
Download data: BW, XLSX
Series
Accession:
GSE42706
ID:
200042706
2.

The Aurora B kinase and the polycomb protein Ring1B combine to regulate active promoters in quiescent lymphocytes [ChIP-seq]

(Submitter supplied) Genome-wide distribution of proteins and histone marks in CD43 negative mouse resting B cells
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
18 Samples
Download data: BW, XLSX
Series
Accession:
GSE42705
ID:
200042705
3.

The Aurora B kinase and the polycomb protein Ring1B combine to regulate active promoters in quiescent lymphocytes [RNA-Seq]

(Submitter supplied) Expression profiling of resting B cells to classify active and silent genes based on expression levels
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: TXT
Series
Accession:
GSE42704
ID:
200042704
4.

Loss of Ring1B catalytic activity causes a pronounced reduction in H3K27me3 deposition yet minimally disrupts the expression of target genes

(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:
GPL10787 GPL13112
21 Samples
Download data: BEDGRAPH, TXT
Series
Accession:
GSE69978
ID:
200069978
5.

Mouse ES cells expressing catalytically inactive Ring1B display impaired Ring1B and H3K27me3 deposition.

(Submitter supplied) ChIP-seq for H3K27me3 and Ring1B was performed in WT mESCs and mESCs containing catalytically inactive Ring1B (I53A mutant). Cells expressing catalytically inactive Ring1B maintain the spatial distribution of Ring1B and H3K27me3 but at reduced levels. These findings support the notion that PRC2 recruitment is, in part, dependent on H2A ubiquitination (H2AK119ub).
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: BEDGRAPH, TXT
Series
Accession:
GSE69955
ID:
200069955
6.

Catalytically inactive Ring1B maintains near wildtype levels of gene expression in mESCs

(Submitter supplied) This experiment was designed to determine the extent of gene misregulation in mESCs containing catalytically dead Ring1B in comparison to mESCs lacking Ring1B.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
9 Samples
Download data: TXT
Series
Accession:
GSE69824
ID:
200069824
7.

Role of remodeling and spacing factor 1 in histone H2A ubiquitination mediated gene silencing

(Submitter supplied) Posttranslational modification of histones plays important roles in regulating chromatin-based nuclear processes. Histone H2A ubiquitination (H2Aub) is a prevalent modification and has been primarily linked to gene silencing; however, the mechanism by which H2Aub represses gene expression remains largely unclear. Here we report the identification of RSF1 (remodeling and spacing factor 1), a subunit of the RSF (remodeling and spacing factor) complex, as a novel H2Aub binding protein which mediates the repressive function of H2Aub on gene expression. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL20301 GPL21103 GPL9250
13 Samples
Download data: TXT, WIG
Series
Accession:
GSE93090
ID:
200093090
8.

Investigation of Rsf1 genomic distribution and effect on gene expression

(Submitter supplied) We report the effect of Rsf1 knockdown or deletion on gene expression in human and mouse cells. We also report the genomic distribution of Rsf1 in mouse embryonic stem cells and nucleosome positioning in wild type and RSF1 knockout mouse ESC.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL17021 GPL16791
11 Samples
Download data: BEDGRAPH, TXT
Series
Accession:
GSE83360
ID:
200083360
9.

Polycomb repressive complex 1 (PRC1) mediated regualtion of uterine stromal cells decidualization.

(Submitter supplied) We extract RNA from mouse implantation sites (IS) on D8 of pregnancy. Mice were treated with or without PRT4165, an inhibitior of PRC1. Total RNAs were analyzed by RNA sequncing.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: CSV
Series
Accession:
GSE80623
ID:
200080623
10.

R-loops and PRC1 repress Polycomb-target genes in mouse embryonic stem cells

(Submitter supplied) R-loops are three-stranded nucleic acid structures that form naturally during transcription, especially over unmethylated CpG-rich promoters. In mESC, such promoters of developmental regulator genes are occupied by the Polycomb-repressor complexes PRC1 and PRC2. Here we have explored the possibility that R-loops form over Polycomb-repressed genes and play a role in their transcriptional silencing. Using single gene and genome-wide analyses, we show that R-loops form at a specific subset of PRC-target genes and contribute to Polycomb occupancy on chromatin. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: BW
Series
Accession:
GSE118115
ID:
200118115
11.

Histone H2AK119 Mono-Ubiquitination is Essential for Polycomb-Mediated Transcriptional Repression

(Submitter supplied) The major function of Polycomb group proteins (PcG) is to maintain transcriptional repression to preserve cellular identity. This is exerted by two distinct repressive complexes, PRC1 and PRC2, that modify histones by depositing H2AK119ub1 and H3K27me3, respectively. Both complexes are essential for development and are deregulated in several types of human tumors. PRC1 and PRC2 exist in different variants and show a complex regulatory cross-talk. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
99 Samples
Download data: BED, TSV
Series
Accession:
GSE134053
ID:
200134053
12.

Ring1B Promotes Hepatic Stem/Progenitor Cell Expansion via Simultaneous Suppression of Cdkn1a and Cdkn2a

(Submitter supplied) The expansion of hepatic stem/progenitor cells requires Ring1B-mediated epigenetic silencing of Cdkn1a and Cdkn2a, demonstrating that Ring1B simultaneously regulates multiple CDKI in tissue stem/progenitor cells.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL5642
1 Sample
Download data: GPR
Series
Accession:
GSE54116
ID:
200054116
13.

Fbxl10 regulates PRC1 recruitment to CpG islands and H2A ubiquitination

(Submitter supplied) Polycomb repressive complex 1 (PRC1) catalyzes H2A monoubiquitination (uH2A) and regulates pluripotency in embryonic stem cells (ESCs). However the mechanisms controlling PRC1 recruitment and activity are largely unknown. Here we show that Fbxl10 interacts with Ring1B and Nspc1, forming a non-canonical PRC1. We demonstrate that Fbxl10-PRC1 is essential for H2A ubiquitination in mouse ESCs. Genome-wide analyses reveal that Fbxl10 preferentially binds to CpG islands and co-localizes with Ring1B on Polycomb target genes. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL9250 GPL13112
11 Samples
Download data: BED
Series
Accession:
GSE37930
ID:
200037930
14.

Genome-wide RING1B binding in Fbxl10 overexpressing 3T3-L1 cells at day 2 of differentiation

(Submitter supplied) We analyzed RING1B binding regions in 3T3-L1 cell lines transduced with the retroviral vector for V5-tagged Fbxl10 or its dF-box mutant.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9185
7 Samples
Download data: BAR
Series
Accession:
GSE64312
ID:
200064312
15.

Expression data from Fbxl10 overexpressing 3T3-L1 cells

(Submitter supplied) Target genes of Fbxl10 during 3T3-L1 adipogenesis was analyzed
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
2 Samples
Download data: CEL, TXT
Series
Accession:
GSE64154
ID:
200064154
16.

Chip-chip from WT and Polycomb Component Knock Out Mouse ES cells for H2AZ, H3K27me3, EZH2 and Ring1B.

(Submitter supplied) The essential histone variant H2A.Z localises to both active and silent chromatin sites. In embryonic stem cells (ESCs), H2A.Z is also reported to co-localise with polycomb repressive complex 2 (PRC2) at developmentally silenced genes. The mechanism of H2A.Z targeting is not clear, but a role for the PRC2 component Suz12 has been suggested. Given this association, we wished to determine if polycomb functionally directs H2A.Z incorporation in ESCs. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL14936
10 Samples
Download data: PAIR, TXT
Series
Accession:
GSE36999
ID:
200036999
17.

Usp16

(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:
GPL15103
4 Samples
Download data
Series
Accession:
GSE62825
ID:
200062825
18.

Usp16 WT and KO RNA-Seq ckit and sca1 positive cells

(Submitter supplied) RNA-seq in wt and Usp16 deleted HSC/P
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15103
2 Samples
Download data: TXT
Series
Accession:
GSE62824
ID:
200062824
19.

Usp16 ChIP-seq of ckit and sca1 positive cells

(Submitter supplied) anti-Usp16 ChIP-seq in ckit and sca1 hematopoietic stem/progenitor cells
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL15103
2 Samples
Download data: TXT
Series
Accession:
GSE62823
ID:
200062823
20.

PCGF6-PRC1 suppresses premature differentiation of embryonic stem cells by silencing germ cell-related genes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL18480
34 Samples
Download data: WIG
Series
Accession:
GSE87485
ID:
200087485
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