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Links from GEO DataSets

Items: 20

1.

Rbfox2 controls autoregulation in RNA binding protein networks

(Submitter supplied) We generated a global analysis of Rbfox2 splicing regulation combined with a highly specific, single nucleotide-resolution Rbfox2 RNA binding map. We found that Rbfox2 regulates the splicing and expression of many previously unknown targets, and particularly a number of RNA binding proteins (RBPs), by modulating alternative splicing coupled-NMD. Based on our observations of RBP-Rbfox2 co-regulation with a polarity predicted by Rbfox2 binding, we propose a model whereby Rbfox2 tunes autoregulatory splicing events to control RBP expression levels and in turn alter their respective splicing networks.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL13112
10 Samples
Download data: BED, BW, TXT
Series
Accession:
GSE54794
ID:
200054794
2.

RBFOX2 alter splicing outcome in distinct binding modes with multiple protein partners

(Submitter supplied) RBFOX2 controls the splicing of a large number of transcripts implicated in cell differentiation and development. Parsing RNA-binding protein datasets, we uncover that RBFOX2 can interact with hnRNPC, hnRNPM and SRSF1 to regulate splicing of a broad range of splicing events using different sequence motifs and binding modes. Using immunoprecipitation, specific RBP knockdown, RNA-seq and splice-sensitive PCR, we show that RBFOX2 can target splice sites using three binding configurations: single, multiple or secondary modes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
24 Samples
Download data: XLSX
3.

Rbfox2-coordinated alternative splicing of Mef2d and Rock2 controls myoblast fusion during myogenesis

(Submitter supplied) Purpose: The goals of this study are to compare transcriptomes using RNA-seq of mouse myoblasts (C2C12 cell line) in undifferentiated and differentiated states and with siRNA-mediated knock down of the RNA binding proteins, Rbfox1 (only expressed in differentiated state) and Rbfox2 (expressed in both undifferentiated and differentiated states). Methods: Differentiated and undifferentiated C2C12 cultures treated with Rbfox1 (differentiated only) or Rbfox2 siRNAs or a mock siRNA transfection were used for RNA-Seq analysis using Illumina HiSeq2000. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
11 Samples
Download data: BEDGRAPH
Series
Accession:
GSE58928
ID:
200058928
4.

Rbfox2 is necessary for cardiovascular development

(Submitter supplied) Purpose: The goal of this study is to investigate the role of Rbfox2, an RNA binding protein in cardiovascular development. Methods: RNA-Seq splicing analysis of mouse embryonic heart at embryonic day 9.5, isolated from control and genetic deletion of either one or both allels of Rbfox2 using Nkx2-5 Cre.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21626
6 Samples
Download data: TAB
Series
Accession:
GSE135152
ID:
200135152
5.

Expression data from human pancreatic cancer cell lines and mouse orthotopic tumors generated using human PDAC cell lines replete and depleted for RBFOX2

(Submitter supplied) RBFOX2 is an RNA binding protein that directs alternative splicing. In this study, we characterized RBFOX2-mediated alternative splicing in pancreatic cancer (PDAC) In this dataset, we assayed gene-level and exon-level expression differences in pancreatic cancer cell lines replete and depleted for RBFOX2 expression and in 8 pairs of orthotopic pancreas tumors and related liver metastases generated from human 4039 or Panc1 cell lines replete or depleted for RBFOX2.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platform:
GPL23126
24 Samples
Download data: CEL
Series
Accession:
GSE211435
ID:
200211435
6.

The RNA-binding landscape of RBM10 and its role in alternative splicing regulation in models of mouse early development

(Submitter supplied) Mutations in the RNA-binding protein, RBM10, result in a human syndromic form of cleft palate, termed TARP syndrome. A role for RBM10 in alternative splicing regulation has been previously demonstrated in human cell lines. To uncover the cellular functions of RBM10 in a cell line that is relevant to the phenotype observed in TARP syndrome, we used iCLIP to identify its endogenous RNA targets in a mouse embryonic mandibular cell line. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL13112
21 Samples
Download data: TXT
Series
Accession:
GSE89270
ID:
200089270
7.

LIN28 binds messenger RNAs at GGAGA motifs and regulates splicing factor abundance

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL9115 GPL9052 GPL15106
26 Samples
Download data: BED, CEL, TXT
Series
Accession:
GSE39873
ID:
200039873
8.

LIN28 binds messenger RNAs at GGAGA motifs and regulates splicing factor abundance (HTS)

(Submitter supplied) LIN28 is a conserved RNA binding protein implicated in pluripotency, reprogramming and oncogenesis. Previously shown to act primarily by blocking let-7 microRNA (miRNA) biogenesis, here we elucidate distinct roles of LIN28 regulation via its direct messenger RNA (mRNA) targets. Through cross-linking and immunoprecipitation coupled with high-throughput sequencing (CLIP-seq) in human embryonic stem cells and somatic cells expressing exogenous LIN28, we have defined discrete LIN28 binding sites in a quarter of human transcripts. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL9115 GPL9052
8 Samples
Download data: BED, TXT
Series
Accession:
GSE39872
ID:
200039872
9.

LIN28 binds messenger RNAs at GGAGA motifs and regulates splicing factor abundance (splicing array)

(Submitter supplied) LIN28 is a conserved RNA binding protein implicated in pluripotency, reprogramming and oncogenesis. Previously shown to act primarily by blocking let-7 microRNA (miRNA) biogenesis, here we elucidate distinct roles of LIN28 regulation via its direct messenger RNA (mRNA) targets. Through cross-linking and immunoprecipitation coupled with high-throughput sequencing (CLIP-seq) in human embryonic stem cells and somatic cells expressing exogenous LIN28, we have defined discrete LIN28 binding sites in a quarter of human transcripts. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15106
18 Samples
Download data: CEL
Series
Accession:
GSE39855
ID:
200039855
10.

Neural crest-specific deletion of splicing factor Rbfox2 leads to craniofacial abnormalities including cleft palate

(Submitter supplied) Alternative splicing (AS) creates proteomic diversity from a limited size genome by generating numerous transcripts from a single protein-coding gene. Tissue-specific regulators of AS are essential components of the gene regulatory network, required for normal cellular function, tissue patterning, and embryonic development. However, their cell-autonomous function in neural crest development has not been explored. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
6 Samples
Download data: TXT
Series
Accession:
GSE127245
ID:
200127245
11.

Alternative RNA Splicing in the Endothelium Mediated in Part by Rbfox2 Regulates the Arterial Response to Low Flow

(Submitter supplied) Low and disturbed blood flow drives the progression of arterial diseases including atherosclerosis and aneurysms. The endothelial response to flow and its interactions with recruited platelets and leukocytes determine disease progression. Here, we report widespread changes in alternative splicing of pre-mRNA in the flow-activated murine arterial endothelium in vivo. Alternative splicing was suppressed by depletion of platelets and macrophages recruited to the arterial endothelium under low and disturbed flow. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL17021 GPL13112 GPL19057
42 Samples
Download data: TXT
Series
Accession:
GSE101826
ID:
200101826
12.

Suppression of RBFox2 by Multiple MiRNAs Contributed to Progressive Heart Failure

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL24247
12 Samples
Download data: TXT
Series
Accession:
GSE215303
ID:
200215303
13.

Suppression of RBFox2 by Multiple MiRNAs Contributed to Progressive Heart Failure (small RNA-Seq)

(Submitter supplied) Heart failure is the final stage of various cardiovascular diseases, which seriously threatens human health. Increasing mediators have been found to be involved in the pathogenesis of heart failure, including RNA binding protein RBFox2. It participates in regulation of cardiac function in multiple aspects and plays a critical role in the process of heart failure. However, how RBFox2 itself is regulated remains unclear. more...
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL24247
8 Samples
Download data: TXT
Series
Accession:
GSE215302
ID:
200215302
14.

Suppression of RBFox2 by Multiple MiRNAs Contributed to Progressive Heart Failure (RNA-Seq)

(Submitter supplied) Heart failure is the final stage of various cardiovascular diseases, which seriously threatens human health. Increasing mediators have been found to be involved in the pathogenesis of heart failure, including RNA binding protein RBFox2. It participates in regulation of cardiac function in multiple aspects and plays a critical role in the process of heart failure. However, how RBFox2 itself is regulated remains unclear. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
4 Samples
Download data: TXT
Series
Accession:
GSE215301
ID:
200215301
15.

Global Promotion of Alternative Internal Exon Usage by mRNA 3' End Formation Factors

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Expression profiling by high throughput sequencing; Other
Platforms:
GPL5188 GPL11154
17 Samples
Download data: BED, CEL, TXT
Series
Accession:
GSE60392
ID:
200060392
16.

Global Regulation of Alternative Internal Exon Usage by mRNA 3' End Formation Factors [RNA-Seq]

(Submitter supplied) RNA-seq analysis of samples from Non-silencing, RBFOX2 and CPSF2 knockdown cells
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: TXT
17.

Global Regulation of Alternative Internal Exon Usage by mRNA 3' End Formation Factors [iCLIP-Seq]

(Submitter supplied) iCLIP was performed in duplicates using RBFOX2 and CPSF2 antibodies.
Organism:
Homo sapiens
Type:
Other
Platform:
GPL11154
2 Samples
Download data: BED
Series
Accession:
GSE60385
ID:
200060385
18.

Global Regulation of Alternative Internal Exon Usage by mRNA 3' End Formation Factors [Affymetrix]

(Submitter supplied) Transcriptome analysis of samples from Non-silencing, RBFOX2 and CPSF3 knockdown cells. Our analysis shows the role of CPSF-SYMPK in regulation of global alternative splicing.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5188
9 Samples
Download data: CEL
Series
Accession:
GSE47465
ID:
200047465
19.

Transcriptome-wide mRNA alterations in Streptozotocin induced Type I diabetic mouse heart

(Submitter supplied) We sequenced mRNA from Left Ventricles of Streptozotocin induced Type I diabetic mouse hearts or mock treated controls at 4 weeks post-treatment in order to assess alternative splicing changes.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15103
5 Samples
Download data: TXT
Series
Accession:
GSE80664
ID:
200080664
20.

Identification of FUS RNA targets in HeLa cells

(Submitter supplied) We identified a landscape of FUS-binding RNA targets in HeLa cells. The majority of the FUS binding sites are in introns of pre-mRNAs and less are in exons and untranslated regions. Significant FUS binding in introns flanking cassette exons, long intron (>100kb) containing transcripts and noncoding RNAs were detected in our study. We specifically determined the function of FUS in regulating the alternative splicing of cassette exons. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL9115
2 Samples
Download data: BED
Series
Accession:
GSE50178
ID:
200050178
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