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Links from GEO DataSets

Items: 20

1.

U1 snRNP increases RNA Pol II elongation rate to enable synthesis of long genes [PRO-seq]

(Submitter supplied) The expansion of introns within mammalian genomes poses a challenge for the production of full-length messenger RNAs (mRNA)s, with increasing evidence that these long AT-rich sequences present obstacles to transcription. Here, we investigate RNAPII elongation in mammalian cells at high resolution and demonstrate that RNAPII transcribes faster across introns. Moreover, we find that this acceleration is mediated by the association of U1 snRNP (U1) with the elongation complex at 5’ splice sites. more...
Organism:
Homo sapiens; Mus musculus
Type:
Other
Platforms:
GPL24247 GPL24676
10 Samples
Download data: BEDGRAPH
Series
Accession:
GSE218128
ID:
200218128
2.

U1 snRNP increases RNA Pol II elongation rate to enable synthesis of long genes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL24247 GPL13112 GPL24676
52 Samples
Download data
Series
Accession:
GSE218135
ID:
200218135
3.

U1 snRNP increases RNA Pol II elongation rate to enable synthesis of long genes [PAC-seq]

(Submitter supplied) The expansion of introns within mammalian genomes poses a challenge for the production of full-length messenger RNAs (mRNA)s, with increasing evidence that these long AT-rich sequences present obstacles to transcription. Here, we investigate RNAPII elongation in mammalian cells at high resolution and demonstrate that RNAPII transcribes faster across introns. Moreover, we find that this acceleration is mediated by the association of U1 snRNP (U1) with the elongation complex at 5’ splice sites. more...
Organism:
Mus musculus
Type:
Other
Platforms:
GPL13112 GPL24247
17 Samples
Download data: BEDGRAPH
Series
Accession:
GSE218134
ID:
200218134
4.

U1 snRNP increases RNA Pol II elongation rate to enable synthesis of long genes [TT-Seq]

(Submitter supplied) The expansion of introns within mammalian genomes poses a challenge for the production of full-length messenger RNAs (mRNA)s, with increasing evidence that these long AT-rich sequences present obstacles to transcription. Here, we investigate RNAPII elongation in mammalian cells at high resolution and demonstrate that RNAPII transcribes faster across introns. Moreover, we find that this acceleration is mediated by the association of U1 snRNP (U1) with the elongation complex at 5’ splice sites. more...
Organism:
Mus musculus; Homo sapiens
Type:
Other
Platforms:
GPL24676 GPL24247
10 Samples
Download data: BEDGRAPH
Series
Accession:
GSE218127
ID:
200218127
5.

U1 snRNP increases RNA Pol II elongation rate to enable synthesis of long genes [ChIP-Seq]

(Submitter supplied) The expansion of introns within mammalian genomes poses a challenge for the production of full-length messenger RNAs (mRNA)s, with increasing evidence that these long AT-rich sequences present obstacles to transcription. Here, we investigate RNAPII elongation in mammalian cells at high resolution and demonstrate that RNAPII transcribes faster across introns. Moreover, we find that this acceleration is mediated by the association of U1 snRNP (U1) with the elongation complex at 5’ splice sites. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
3 Samples
Download data: BEDGRAPH
Series
Accession:
GSE218126
ID:
200218126
6.

U1 snRNP increases RNA Pol II elongation rate to enable synthesis of long genes [RNA-Seq]

(Submitter supplied) The expansion of introns within mammalian genomes poses a challenge for the production of full-length messenger RNAs (mRNA)s, with increasing evidence that these long AT-rich sequences present obstacles to transcription. Here, we investigate RNAPII elongation in mammalian cells at high resolution and demonstrate that RNAPII transcribes faster across introns. Moreover, we find that this acceleration is mediated by the association of U1 snRNP (U1) with the elongation complex at 5’ splice sites. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL24247 GPL24676
12 Samples
Download data: BEDGRAPH
Series
Accession:
GSE218125
ID:
200218125
7.

Transcriptional Pause Sites Delineate Stable Nucleosome-Associated Premature Polyadenylation Suppressed by U1 snRNP [2P-seq, Pabpn1 CKO]

(Submitter supplied) Regulation of RNA polymerase II (Pol II) elongation is a critical step in gene regulation. Here, we report that U1 snRNP recognition and transcription pausing at stable nucleosomes are linked through premature polyadenylation signal (PAS) termination. By generating RNA exosome conditional deletion mouse embryonic stem cells, we identified a large class of polyadenylated short transcripts in the sense direction destabilized by the RNA exosome. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL19057
4 Samples
Download data: BW
Series
Accession:
GSE107132
ID:
200107132
8.

Transcriptional Pause Sites Delineate Stable Nucleosome-Associated Premature Polyadenylation Suppressed by U1 snRNP

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL19057
20 Samples
Download data: BW
Series
Accession:
GSE100537
ID:
200100537
9.

Transcriptional Pause Sites Delineate Stable Nucleosome-Associated Premature Polyadenylation Suppressed by U1 snRNP [2P-seq]

(Submitter supplied) Regulation of RNA polymerase II (Pol II) elongation is a critical step in gene regulation. Here, we report that U1 snRNP recognition and transcription pausing at stable nucleosomes are linked through premature polyadenylation signal (PAS) termination. By generating RNA exosome conditional deletion mouse embryonic stem cells, we identified a large class of polyadenylated short transcripts in the sense direction destabilized by the RNA exosome. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL19057
12 Samples
Download data: BW, TXT
Series
Accession:
GSE100536
ID:
200100536
10.

Transcriptional Pause Sites Delineate Stable Nucleosome-Associated Premature Polyadenylation Suppressed by U1 snRNP [RNA-seq]

(Submitter supplied) Regulation of RNA polymerase II (Pol II) elongation is a critical step in gene regulation. Here, we report that U1 snRNP recognition and transcription pausing at stable nucleosomes are linked through premature polyadenylation signal (PAS) termination. By generating RNA exosome conditional deletion mouse embryonic stem cells, we identified a large class of polyadenylated short transcripts in the sense direction destabilized by the RNA exosome. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
4 Samples
Download data: BW, TXT
Series
Accession:
GSE100535
ID:
200100535
11.

U1 snRNP regulates chromatin retention of noncoding RNAs

(Submitter supplied) Pervasive transcription in the mammalian genome produces thousands of long noncoding RNAs (lncRNAs) and promoter- or enhancer-associated unstable transcripts. They preferentially locate to chromatin, at which some regulate chromatin structure, transcription and RNA processing. While several RNA sequences responsible for nuclear localization have been identified, such as repeats in the lncRNA Xist and Alu-like elements for long RNAs, how lncRNAs as a class are enriched on chromatin remains elusive. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL21273
112 Samples
Download data: BED, BW, TXT
Series
Accession:
GSE134287
ID:
200134287
12.

U1 snRNP regulates chromatin retention of noncoding RNAs

(Submitter supplied) RNA subcellular localization often correlates with its function and regulation. For many long noncoding RNAs (lncRNAs) and some isoforms of coding genes, their transcripts are preferentially retained on the chromatin. However, the mechanisms controlling the chromatin retention of lncRNAs and mRNA transcripts remain largely unknown. We hypothesize that embedded RNA sequences and interacting proteins may be the cis and trans regulators governing RNA subcellular localization, respectively. more...
Organism:
Homo sapiens; Mus musculus
Type:
Other
Platforms:
GPL20795 GPL21273
12 Samples
Download data: TXT
Series
Accession:
GSE107131
ID:
200107131
13.

Efficient RNA polymerase II pause release requires U2 snRNP function

(Submitter supplied) Transcription by RNA polymerase II (Pol II) is coupled to pre-mRNA splicing, but the underlying mechanisms remain poorly understood. Co-transcriptional splicing requires assembly of a functional spliceosome on nascent pre-mRNA, but whether and how this influences Pol II transcription remains unclear. Here we show that inhibition of pre-mRNA branch site recognition by the spliceosome component U2 snRNP leads to a widespread and strong decrease in new RNA synthesis in human cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18573 GPL21697
48 Samples
Download data: BW, GTF
Series
Accession:
GSE148433
ID:
200148433
14.

iCLIP and NGS to map protein-RNA interactions for U1-snRNP proteins in Trypanosoma brucei

(Submitter supplied) Individual-nucleotide resolution UV-crosslinking and immunoprecipitation (iCLIP) combined with high-throughput sequencing was performed to generate genome-wide binding maps of two U1-snRNP proteins: U1C and U1-70K in Trypanosoma brucei.
Organism:
Trypanosoma brucei
Type:
Other
Platforms:
GPL16563 GPL16562 GPL16561
5 Samples
Download data: TXT
Series
Accession:
GSE43848
ID:
200043848
15.

Intron looping is mediated by U1 snRNP and RNA polymerase II co-transcriptionally

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
18 Samples
Download data: BEDGRAPH, BW, TXT
Series
Accession:
GSE145092
ID:
200145092
16.

Intron looping is mediated during transcription by U1 snRNP and RNA polymerase II [RNA-Seq]

(Submitter supplied) In the earliest step of spliceosome assembly, the two splice sites flanking an intron are brought into proximity by U1 snRNP and U2AF. The mechanism that facilitates this intron looping is poorly understood. Using a CRISPR interference-based approach to halt RNA polymerase II transcription in the middle of introns, we discovered that the 5 splice site base pairs with a U1 snRNA that is tethered to RNA polymerase II during intron synthesis. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
1 Sample
Download data: TXT
Series
Accession:
GSE144906
ID:
200144906
17.

Intron looping is mediated during transcription by U1 snRNP and RNA polymerase II [RIP-seq]

(Submitter supplied) In the earliest step of spliceosome assembly, the two splice sites flanking an intron are brought into proximity by U1 snRNP and U2AF. The mechanism that facilitates this intron looping is poorly understood. Using a CRISPR interference-based approach to halt RNA polymerase II transcription in the middle of introns, we discovered that the 5 splice site base pairs with a U1 snRNA that is tethered to RNA polymerase II during intron synthesis. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
10 Samples
Download data: BEDGRAPH, BW
18.

Intron looping is mediated by U1 snRNP and RNA polymerase II co-transcriptionally [ChIP-seq]

(Submitter supplied) In the earliest step of spliceosome assembly, the two splice sites flanking an intron are brought into proximity by U1 snRNP and U2AF. The mechanism that facilitates this intron looping is poorly understood. Using a CRISPR interference-based approach to halt RNA polymerase II transcription in the middle of introns, we discovered that the 5 splice site base pairs with a U1 snRNA that is tethered to RNA polymerase II during intron synthesis. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
7 Samples
Download data: BW
Series
Accession:
GSE144874
ID:
200144874
19.

Transcriptome changes in splicing inhibited cells

(Submitter supplied) In eukaryotes, U1 small nuclear ribonucleoprotein (snRNP) forms spliceosomes in equal stoichiometry with U2, U4, U5 and U6 snRNPs; however, its abundance in human far exceeds that of the other snRNPs. Here we used antisense morpholino oligonucleotide to U1 snRNA to achieve functional U1 snRNP knockdown in HeLa cells, and identified accumulated unspliced pre-mRNAs by genomic tiling microarrays. In addition to inhibiting splicing, U1 snRNP knockdown caused premature cleavage and polyadenylation in numerous pre-mRNAs at cryptic polyadenylation signals, frequently in introns near (<5 kilobases) the start of the transcript. more...
Organism:
Homo sapiens
Type:
Expression profiling by genome tiling array
Platform:
GPL4914
3 Samples
Download data: BAR, CEL
Series
Accession:
GSE24179
ID:
200024179
20.

U1 snRNP complex with cleavage and polyadenylation factors controls mRNA transcription termination

(Submitter supplied) Full-length transcription in the majority of human genes depends on U1 snRNP (U1) to co-transcriptionally suppress transcription-terminating premature 3’-end cleavage and polyadenylation (PCPA) from cryptic polyadenylation signals (PASs) in introns. However, the mechanism of this U1 activity, termed telescripting, is unknown. Here, we captured a complex, comprising U1 and CPA factors (U1–CPAFs), that binds intronic PASs and suppresses PCPA. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
22 Samples
Download data: BW
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