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Links from GEO DataSets

Items: 20

1.

Transcriptome analysis of SFP45 knockdown cells

(Submitter supplied) Examination of transcriptome of SPF45 knockdown cells by Ribosomal RNA depleted RNA-Seq
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
6 Samples
Download data: BW
2.

Transcriptome analysis of SAP30BP knockdown cells

(Submitter supplied) Examination of transcriptome of SAP30BP knockdown cells by Ribosomal RNA depleted RNA-Seq
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
6 Samples
Download data: BEDGRAPH
Series
Accession:
GSE220906
ID:
200220906
3.

iCLIP-based modeling uncovers 3’ splice site definition: how U2AF65 specificity relies on regulation by co-factors

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
synthetic gene; Homo sapiens
Type:
Other
Platforms:
GPL16791 GPL23545
79 Samples
Download data: BEDGRAPH, BW
Series
Accession:
GSE99700
ID:
200099700
4.

iCLIP-based modeling uncovers 3’ splice site definition: how U2AF65 specificity relies on regulation by co-factors [in vitro iCLIP]

(Submitter supplied) Alternative splicing generates distinct mRNA isoforms and is crucial for proteome diversity in eukaryotes. The RNA-binding protein (RBP) U2AF65 is central to splicing decisions, as it recognizes 3' splice sites and recruits the spliceosome. We established 'in vitro iCLIP' experiments, in which recombinant RBPs are incubated with long transcripts, to study how U2AF65 recognizes RNA sequences and how this is modulated by trans-acting RBPs. more...
Organism:
synthetic gene
Type:
Other
Platform:
GPL23545
31 Samples
Download data: BED, BW
Series
Accession:
GSE99698
ID:
200099698
5.

iCLIP-based modeling uncovers 3’ splice site definition: how U2AF65 specificity relies on regulation by co-factors [in vitro iCLIP co-factors]

(Submitter supplied) Alternative splicing generates distinct mRNA isoforms and is crucial for proteome diversity in eukaryotes. The RNA-binding protein (RBP) U2AF65 is central to splicing decisions, as it recognizes 3' splice sites and recruits the spliceosome. We established 'in vitro iCLIP' experiments, in which recombinant RBPs are incubated with long transcripts, to study how U2AF65 recognizes RNA sequences and how this is modulated by trans-acting RBPs. more...
Organism:
synthetic gene
Type:
Other
Platform:
GPL23545
37 Samples
Download data: BEDGRAPH, BW
Series
Accession:
GSE99696
ID:
200099696
6.

iCLIP-based modeling uncovers 3’ splice site definition: how U2AF65 specificity relies on regulation by co-factors [in vivo iCLIP]

(Submitter supplied) Alternative splicing generates distinct mRNA isoforms and is crucial for proteome diversity in eukaryotes. The RNA-binding protein (RBP) U2AF65 is central to splicing decisions, as it recognizes 3' splice sites and recruits the spliceosome. We established 'in vitro iCLIP' experiments, in which recombinant RBPs are incubated with long transcripts, to study how U2AF65 recognizes RNA sequences and how this is modulated by trans-acting RBPs. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL16791
11 Samples
Download data: BW
7.

Alternative splicing factor hnRNPA1 induces U2AF2 association with Alu-derived RNA

(Submitter supplied) Alternative splicing drives transcriptome and proteome diversification. While splicing regulatory proteins govern this process, their global mechanisms remain enigmatic. We generated high resolution transcriptome-wide protein-RNA interaction maps to determine how the splicing repressor hnRNPA1 influences the global association of spliceosome assembly factor U2AF2 and SRSF1 with pre-mRNA. We observed changes in the distribution of U2AF2 crosslinking sites relative to the 3’ splice sites of cassette exons but not constitutive exons upon hnRNPA1 overexpression. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
20 Samples
Download data: BED, TXT
8.

Oncogenic MYC induces a dependency on the spliceosome in human cancer

(Submitter supplied) c-MYC (MYC) overexpression or hyperactivation is one of the most common drivers of human cancer. Despite intensive study, the MYC oncogene remains recalcitrant to therapeutic inhibition. Like other classic oncogenes, hyperactivation of MYC leads to collateral stresses onto cancer cells, suggesting that tumors harbor unique vulnerabilities arising from oncogenic activation of MYC. Herein, we discover the spliceosome as a new target of oncogenic stress in MYC-driven cancers. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
11 Samples
Download data: TXT
9.

Total and chromatin-associated RNA (totalRNA and chRNA) sequencing experiments upon rapid depletion of endogenous DHX15 or DHX38

(Submitter supplied) To investigate DHX15's functions in splicing QC in human cells, we induced rapid proteolysis-mediated depletion of endogenous DHX15 and DHX38 and performed high-throughput sequencing of totalRNA and chRNA.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL24676
48 Samples
Download data: TSV
10.

Dissolution of RNA condensates by the embryonic stem cell protein L1TD1

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL18573
15 Samples
Download data: BEDGRAPH
Series
Accession:
GSE227856
ID:
200227856
11.

Dissolution of RNA condensates by the embryonic stem cell protein L1TD1 [RNA-seq]

(Submitter supplied) L1TD1 is a cytoplasmic RNA-binding protein that is specifically expressed in pluripotent stem cells and, unlike its mouse paralogue, is essential for the maintenance of stemness in human cells. Although L1TD1 is the only known domesticated gene from a LINE-1 (L1) retroelement, the functional legacy from its ancestral protein, ORF1p of L1, and the novelty are so far unknown. Here, we determined RNAs associated with L1TD1 and found that, like ORF1p, L1TD1 binds L1 RNAs, localizes to high-density ribonucleoprotein (RNP) condensates, and increases L1 retrotransposition. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
7 Samples
Download data: BEDGRAPH
Series
Accession:
GSE227854
ID:
200227854
12.

Global analysis of binding sites of U2AF1 and ZRSR2 reveals RNA elements required for mutually exclusive splicing by the U2- and U12-type spliceosome

(Submitter supplied) Eukaryotic nuclear introns have been dichotomously classified into common U2-type introns and rare U12-type introns. Because the highly conserved consensus sequences for the 5’ splice site and the branch point are found within all U12-type introns, weighted matrices for these motifs are used for prediction of U12-type introns. However, the U12-type consensus sequences per se are also recognized by the U2-type spliceosome. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL18573
11 Samples
Download data: BEDGRAPH
Series
Accession:
GSE203531
ID:
200203531
13.

RBM5 and RBM10

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Other; Expression profiling by high throughput sequencing
Platform:
GPL20301
25 Samples
Download data: BW
Series
Accession:
GSE240608
ID:
200240608
14.

RNP-seq and IP-seq from cells expressing epitope-tagged RBM5, RBM10, or SF3A3

(Submitter supplied) We isolated snRNP complexes derived from precatalytic A or B-like spliceosomes solubilized from the chromatin pellet of lysed nuclei. These complexes contained U2 snRNP proteins and a portion of the U2 snRNA, bound with intronic branch sites prior to the first catalytic step of splicing. The complexes have similar composition, whether directly isolated from extracted material, or after selection from glycerol gradients. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL20301
13 Samples
Download data: BW, XLSX
Series
Accession:
GSE240596
ID:
200240596
15.

Identification of RBM5 and RBM10-dependent splicing events in 293Flp-In cells.

(Submitter supplied) RBM5 and RBM10 are RNA-binding proteins and splicing regulators. These two proteins are putative paralogs in mammalian cells, sharing common domain organization and extensive protein sequence similarity, but their RNA-binding preferences differ. We developed a sensitive system to identify splicing events regulated by RBM5 and/or RBM10, deleting all RBM5 alleles in 293Flp-In cells, and reducing the expression of RBM10, which is partially rescued by activation of a cryptic exon (CE) in one of the RBM10 alleles. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
12 Samples
Download data: XLSX
Series
Accession:
GSE240259
ID:
200240259
16.

The histone variant H2A.Z promotes efficient co-transcriptional splicing in S. cerevisiae

(Submitter supplied) In eukaryotes, a dynamic ribonucleic protein machine known as the spliceosome catalyzes the removal of introns from pre-messenger RNA (pre-mRNA). Recent studies show the process of RNA-synthesis and RNA-processing to be spatio-temporally coordinated, indicating that RNA splicing takes place in the context of chromatin. H2A.Z is a highly conserved histone variant of the canonical histone H2A. In S. cerevisiae, H2A.Z is deposited into chromatin by the SWR1-complex, is found near the 5’ ends of protein-coding genes, and has been implicated in transcription regulation. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13821
15 Samples
Download data: XLSX
Series
Accession:
GSE97416
ID:
200097416
17.

SF3B1 association with chromatin determines splicing outcomes

(Submitter supplied) Much remains unknown concerning the mechanism by which the splicing machinery pinpoints short exons within intronic sequences and how splicing factors are directed to their pre-mRNA targets. Part of the explanation probably lies in differences in chromatin organization between exons and introns. Proteomic, co-immunoprecipitation, and sedimentation analyses described here indicated that SF3B1, an essential splicing component of the U2 snRNP complex, is strongly associated with nucleosomes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: TXT, WIG
Series
Accession:
GSE65644
ID:
200065644
18.

FUBP1 is a core splicing factor that facilitates 3' splice site recognition and splicing of long introns

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
synthetic construct; Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL19424 GPL11154 GPL18573
61 Samples
Download data: BW
Series
Accession:
GSE220186
ID:
200220186
19.

FUBP1 is a core splicing factor that facilitates 3' splice site recognition and splicing of long introns [In vivo iCLIP]

(Submitter supplied) Splicing is a central process in metazoans and greatly expands their proteome by alternative splicing of pre-mRNA transcripts. An essential regulatory step during early spliceosome assembly is the recognition of cis-regulatory RNA motifs in pre-mRNAs. Here, we identified the RNA binding protein FUBP1 as a novel core splicing factor with a ubiquitous footprint on pre-mRNAs. FUBP1 binds to a previously unknown cis-regulatory motif upstream of the branch point of human introns. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
27 Samples
Download data: BW
Series
Accession:
GSE220184
ID:
200220184
20.

FUBP1 is a core splicing factor that facilitates 3' splice site recognition and splicing of long introns [In vitro iCLIP]

(Submitter supplied) Splicing is a central process in metazoans and greatly expands their proteome by alternative splicing of pre-mRNA transcripts. An essential regulatory step during early spliceosome assembly is the recognition of cis-regulatory RNA motifs in pre-mRNAs. Here, we identified the RNA binding protein FUBP1 as a novel core splicing factor with a ubiquitous footprint on pre-mRNAs. FUBP1 binds to a previously unknown cis-regulatory motif upstream of the branch point of human introns. more...
Organism:
synthetic construct
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19424
18 Samples
Download data: BED, BW
Series
Accession:
GSE220183
ID:
200220183
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