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Links from GEO DataSets

Items: 20

1.

Murine Myeloid-Erythroid Progenitors (MEPs): WT vs. Bmi1-/-

(Submitter supplied) Transcriptional profiling of MEPs purified from wild type and Bmi1-/- mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7042
3 Samples
Download data: TXT
Series
Accession:
GSE63411
ID:
200063411
2.

Murine Proerythroblasts (ProEs): WT vs. Bmi1-/-

(Submitter supplied) Transcriptional profiling of ProEs purified from wild type and Bmi1-/- mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7042
3 Samples
Download data: TXT
Series
Accession:
GSE63413
ID:
200063413
3.

p53 activation during ribosome biogenesis regulates normal erythroid differentiation.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL22936 GPL18573
26 Samples
Download data: CEL, WIG
Series
Accession:
GSE157210
ID:
200157210
4.

p53 activation during ribosome biogenesis regulates normal erythroid differentiation. [ChIP-Seq]

(Submitter supplied) The role of ribosome biogenesis in erythroid development is supported by the recognition of erythroid defects in ribosomopathies in both Diamond-Blackfan anemia and 5q- syndrome. Whether ribosome biogenesis exerts a regulatory function on normal erythroid development is still unknown. In the present study, a detailed characterization of ribosome biogenesis dynamics during human and murine erythropoiesis shows that ribosome biogenesis is abruptly interrupted by the drop of rDNA transcription and the collapse of ribosomal protein neo-synthesis. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
4 Samples
Download data: WIG
Series
Accession:
GSE157208
ID:
200157208
5.

p53 activation during ribosome biogenesis regulates normal erythroid differentiation. [expression]

(Submitter supplied) The role of ribosome biogenesis in erythroid development is supported by the recognition of erythroid defects in ribosomopathies in both Diamond-Blackfan anemia and 5q- syndrome. Whether ribosome biogenesis exerts a regulatory function on normal erythroid development is still unknown. In the present study, a detailed characterization of ribosome biogenesis dynamics during human and murine erythropoiesis shows that ribosome biogenesis is abruptly interrupted by the drop of rDNA transcription and the collapse of ribosomal protein neo-synthesis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL22936
22 Samples
Download data: CEL
Series
Accession:
GSE137951
ID:
200137951
6.

Polycomb Group Protein Bmi1 Promotes Hematopoietic Cell Development from ES Cells

(Submitter supplied) Bmi1 is a component of the Polycomb-repressive complexes (PRC) and essential for maintaining the pool of adult stem cells. PRC are key regulators for embryonic development by modifying chromatin architecture and maintaining gene repression. To assess the role of Bmi1 in pluripotent stem cells and upon exit from pluripotency during differentiation, we studied forced Bmi1 expression in mouse embryonic stem cells (ESC). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4211
Platform:
GPL1261
8 Samples
Download data: CEL
Series
Accession:
GSE20958
ID:
200020958
7.
Full record GDS4211

Polycomb repressive complex 1 protein Bmi1 transduced CCE embryonic stem cells and differentiated embryoid body samples

Analysis of Bmi1 transduced CCE embryonic stem cells (ESC) and CCE ESC differentiated by embryoid body assay. Bmi1 is essential for maintaining the pool of adult stem cells. Results provide insight into role of Bmi1 in ESC-derived hematopoietic cell transition from pluripotency to differentiation.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 5 genotype/variation sets
Platform:
GPL1261
Series:
GSE20958
8 Samples
Download data: CEL
DataSet
Accession:
GDS4211
ID:
4211
8.

Bmi1 suppresses adipogenesis in the hematopoietic stem cell niche

(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
24 Samples
Download data: BEDGRAPH
Series
Accession:
GSE121290
ID:
200121290
9.

Bmi1 suppresses adipogenesis in the hematopoietic stem cell niche: RNA-Seq

(Submitter supplied) Bone marrow mesenchymal stromal cells (MSCs) that express high levels of stem cell factor (SCF) and CXC chemokine ligand 12 (CXCL12) are one crucial component of the hematopoietic stem cell (HSC) niche. While the secreted factors produced by MSCs to support HSCs have been well described, little is known regarding the transcriptional regulators controlling the cell fate of MSCs and thus indirectly maintaining HSCs. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: CSV
Series
Accession:
GSE121288
ID:
200121288
10.

Bmi1 defines long-term adult cardiac stem cells in heart homeostasis and repair

(Submitter supplied) We have found the existence of a Bmi1+ population in the adult heart contributing to the organ low-rate turnover and repair with the generation of new cardiomyocytes. We show that the Bmi1+ population is a sub-population of the cardiac Sca-1+ progenitor cells. We have analyzed the gene profile by deep-sequencing (RNA-Seq) of Bmi1+ and Sca-1+Bmi1- cells in homeostatic heart condition. On the other hand, we have compared gene profile by deep-sequencing (RNA-Seq) of Bmi1+ cells in homeostatic condition versus Bmi1+ cells 5 days after myocardial infarction (MI). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11002
12 Samples
Download data: XLS
Series
Accession:
GSE55754
ID:
200055754
11.

Consequences of Ribosomal Protein Haploinsufficiency in Human Hematopoiesis

(Submitter supplied) Ribosomal protein haploinsufficiency (RPH) underlies diverse human diseases with distinct and specific phenotypes, including Diamond-Blackfan anemia (DBA). Although multiple mechanisms have been proposed for the erythroid-specific hematopoietic defects observed in DBA, only recently has the role of selectively impaired translation been highlighted in these phenotypes. Exactly how and to what extent this impairment of translation occurs is currently unknown. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL16791
14 Samples
Download data: TXT
12.

Expression data from Bmi1-null c-Kit+Sca-1+Lineage marker- (KSL) hematopoietic stem/progenitor cells

(Submitter supplied) Bmi1 is a component of polycomb repressive complex 1 and its role in the inheritance of the stemness of adult somatic stem cells has been well characterized. Bmi1 maintains the self-renewal capacity of adult stem cells, at least partially, by repressing the Ink4a/Arf locus that encodes a cyclin-dependent kinase inhibitor, p16Ink4a, and a tumor suppressor, p19Arf 14. Deletion of both Ink4a and Arf in Bmi1-deficient mice substantially restored the defective self-renewal capacity of HSCs and neural stem cells.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
7 Samples
Download data: CEL, CHP
Series
Accession:
GSE19796
ID:
200019796
13.

Single-cell profiling of human bone marrow progenitors reveals mechanisms of failing erythropoiesis in Diamond-Blackfan anemia

(Submitter supplied) Ribosome dysfunction underlies the pathogenesis of many cancers and heritable ribosomopathies. Here we investigate how mutations in either ribosomal protein large (RPL) or ribosomal protein small (RPS) subunit genes selectively affect erythroid progenitor development and clinical phenotypes in Diamond-Blackfan anemia (DBA), a rare ribosomopathy with limited therapeutic options. Using single-cell assays of patient-derived bone marrow, we delineated two distinct cellular trajectories segregating with ribosomal protein genotypes: almost complete loss of erythroid specification were observed in RPS-DBA. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
8 Samples
Download data: CSV
Series
Accession:
GSE181830
ID:
200181830
14.

Mechanisms of failing erythropoiesis in Diamond-Blackfan anemia revealed by single cell profiling of human bone marrow progenitors

(Submitter supplied) Single-cell RNAseq of CD34+Lineage negative hematopoietic stem and progenitor healthy control and DBA was performed to elucidate the transcriptional features of DBA haematopoiesis.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL21697 GPL24676
9 Samples
Download data: H5AD, TXT
Series
Accession:
GSE156441
ID:
200156441
15.

Genome-wide expression profiling of cells infected with control or RPS14 shRNAs

(Submitter supplied) We performed genome-wide expression profiling of cells infected with control or RPS14 shRNAs. Keywords: controls vs. shRNA treated
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL3921
24 Samples
Download data: CEL, EXP
Series
Accession:
GSE9487
ID:
200009487
16.

Bach Factors Operate Erythro-Myeloid Differentiation by Responding to Infection

(Submitter supplied) Hematopoietic cell differentiation should be tightly regulated in accordance with environmental changes to keep homeostasis. Infection is one of the conditions that induce myelopoiesis to exclude pathogens and repress erythropoiesis, which might be beneficial for the restriction of nutritional iron for pathogens. While several transcription factors (TFs), including C/EBP family and Gata1, play central roles in erythro-myeloid differentiation, the precise mechanism which controls the differentiation for the adaptation to infection remains obscure. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
6 Samples
Download data: TXT
Series
Accession:
GSE86253
ID:
200086253
17.

Investigation of Bach2 function by regulating inflammatory response and heme-iron homeostasis of bone marrow macrophage.

(Submitter supplied) Macrophages are central in regulating iron homeostasis. Transcription repressor Bach2 regulates by heme. Here we investigated the relationship between heme-regulated Bach2 and macrophage in bone marrow. We identified RFP-positive and negative macrophage were in bone marrow. We found that RFP-positive macrophage related with iron-heme homeostasis maintenance and RPF-negative population related with immune response. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13912
6 Samples
Download data: TXT
Series
Accession:
GSE79697
ID:
200079697
18.

BMI1 stress-related functions contribute to the redox-dependent fate of adult cardiac progenitors

(Submitter supplied) The accumulation of reactive oxygen species (ROS) is linked to several cardiovascular pathologies; it is also associated with cell cycle exit by nenonatal cardiomyocytes, a key limiting factor in the regenerative capacity of the adult mammalian heart. BMI1 is a component of the polycomb complex 1, which is linked to adult multipotent progenitors, and is also an important partner in DNA repair and redox regulation. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
14 Samples
Download data: BED
Series
Accession:
GSE92700
ID:
200092700
19.

Identification of Bmi1 regulated genes in pro-B cells

(Submitter supplied) We report differences in gene expression between WT and Bmi1 KO pro-B cells.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: DIFF
Series
Accession:
GSE119422
ID:
200119422
20.

Rules governing translation selectivity under limiting ribosome availability

(Submitter supplied) Ribosomopathies are cell-type-specific pathologies related to a ribosomal protein (RP) gene insult. The 5q- syndrome is a somatic ribosomopathy linked to RPS14 gene haploinsufficiency and characterized by a prominent erythroid hypoplasia. Using quantitative proteomic, we show that GATA1 protein expression is low in shRPS14 cells in which ribosome quantities are diminished. Here, we investigated the cause of low GATA1 protein expression in limiting ribosome availability. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL24299
6 Samples
Download data: CEL, TXT
Series
Accession:
GSE124800
ID:
200124800
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