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Links from GEO DataSets

Items: 15

1.

A p53-dependent translational program directs tissue-selective phenotypes in a model of ribosomopathies

(Submitter supplied) In ribosomopathies, perturbed expression of ribosome components leads to tissue-specific phenotypes. What accounts for such tissue-selective manifestations as a result of mutations in the ribosome, a ubiquitous cellular machine, has remained a mystery. Combining mouse genetics and in vivo ribosome profiling, we observe limb patterning phenotypes in ribosomal protein (RP) haploinsufficient embryos and uncover selective translational changes of transcripts controlling limb development. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL19057
24 Samples
Download data: CSV
Series
Accession:
GSE135722
ID:
200135722
2.

Translational control of mTOR/4E-BP1 axis in MiaPaca-2 cells

(Submitter supplied) Pancreatic ductal adenocarcinoma (PDAC) relies on hyper-activated protein synthesis. Consistently, human and mouse PDAC lose expression of the translational repressor and mTOR target 4E-BP1. Using genome-wide polysome-profiling, we here explore mRNAs whose translational efficiencies depend on the mTOR/4E-BP1 axis in Miapaca-2 cells. This was performed by isolating cytoplasmic and efficiently translated (heavy polysome-associated) mRNAs from MiaPaca-2 cells upon PP242-mediated mTOR inhibition
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
16 Samples
Download data: CEL
Series
Accession:
GSE137553
ID:
200137553
3.

Surveillance of rRNA synthesis by an RNA helicase mediates tissue-specific developmental disorders

(Submitter supplied) Myriad of craniofacial disorders are caused by heterozygous mutations in general regulators of housekeeping cellular functions such as ribosome biogenesis. While it is understood that many of these highly tissue-specific malformations are a consequence of defects in cranial neural crest cells (cNCCs), an embryonic cell group that gives rise to most of the facial structures during embryogenesis, the mechanism underlying cell type-selectivity of these effects remains largely unknown. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL16791
10 Samples
Download data: BW, WIG
Series
Accession:
GSE89420
ID:
200089420
4.

Ribosomal biogenesis genes play an essential and p53-independent role in pancreas development

(Submitter supplied) Analysis of transcriptional profiles in Sbds(ATG) MO-injected embryos with and without coinjection of p53(ATG) MO. We identified a large number of changes in transcript abundance associated with loss of Sbds. Among the 24,278 annotated zebrafish genes in the platform, 4,892 significantly differentially expressed genes were identified.
Organism:
Danio rerio
Type:
Expression profiling by array
Platform:
GPL14688
16 Samples
Download data: TXT
Series
Accession:
GSE39399
ID:
200039399
5.

MYSM1

(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 GPL13112
61 Samples
Download data: BW, TXT
Series
Accession:
GSE150667
ID:
200150667
6.

MYSM1 maintains ribosomal protein gene expression in hematopoietic stem cells to prevent hematopoietic dysfunction II.

(Submitter supplied) MYSM1 is a transcriptional regulator essential for HSC function and hematopoiesis. We established that HSC dysfunction in Mysm1-deficiency is driven by p53 stress response, however, the molecular function of MYSM1 as a transcriptional activator and its essential role in p53 stress response repression remain difficult to reconcile. Here, we performed genome-wide analyses of MYSM1-regulated genes in hematopoietic stem and progenitor cells (HSPCs). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
24 Samples
Download data: TXT
Series
Accession:
GSE150666
ID:
200150666
7.

MYSM1 maintains ribosomal protein gene expression in hematopoietic stem cells to prevent hematopoietic dysfunction I.

(Submitter supplied) MYSM1 is a transcriptional regulator essential for HSC function and hematopoiesis. We established that HSC dysfunction in Mysm1-deficiency is driven by p53 stress response, however, the molecular function of MYSM1 as a transcriptional activator and its essential role in p53 stress response repression remain difficult to reconcile. Here, we performed genome-wide analyses of MYSM1-regulated genes in hematopoietic stem and progenitor cells (HSPCs). more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
8 Samples
Download data: BED, BW
Series
Accession:
GSE150663
ID:
200150663
8.

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
9.

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
10.

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
11.

Expression data from discodermolide sensitive and resistant cell lines

(Submitter supplied) Discodermolide treatment of A549 results in senescence. We compared cells resistant to disco-induced senescence to those that are sensitive to senescence induction. We also examined the gene expression of resistant (AD32) cells overexpressing 4E-BP1, a protein known to restore sensitivity to discodermolide in these cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
10 Samples
Download data: CEL
Series
Accession:
GSE25904
ID:
200025904
12.

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
13.

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
14.

Heterogeneous ribosomes exist and selectively translate distinct subpools of mRNAs in stem cells

(Submitter supplied) Emerging studies have linked the ribosome to more selective control of gene regulation. However, an outstanding question is whether ribosome heterogeneity at the level of core ribosomal proteins (RPs) enables ribosomes to preferentially translate specific mRNAs genome-wide. Here, we measured the absolute abundance of RPs in translating ribosomes and profiled transcripts that are enriched or depleted from select subsets of ribosomes within embryonic stem cells. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL19057
20 Samples
Download data: TXT
Series
Accession:
GSE73357
ID:
200073357
15.

Gene expression changes in limb buds of Nipbl-haploinsufficient mice

(Submitter supplied) Multiple genes are dysregulated in hindlimb buds of Nipbl-deficient embryos. In all, more than 1000 limb bud genes were found to be significantly altered in expression by microarray analysis of E10.5 mouse hindlimb buds. Small changes in expression (mostly decreases) were observed for genes involved in FGF, BMP, and SHH pathways, as well as numerous genes involved in the Wnt/planar cell polarity signaling pathway. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
24 Samples
Download data: CEL
Series
Accession:
GSE60932
ID:
200060932
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