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Links from GEO DataSets

Items: 20

1.

Cryptic introns in lncRNAs recruit conserved Pir2/ARS2 protein to promote gene repression [smRNA-seq]

(Submitter supplied) Long non-coding RNAs (lncRNAs) dynamically regulate gene expression during development and in response to environmental conditions. In S. pombe, lncRNAs repress the expression of nearby genes via a mechanism involving silencing effector proteins. In this study, we find that invasion of a lncRNA into the neighboring gene results in inclusion of a cryptic intron that is required for its repressive activity. more...
Organism:
Schizosaccharomyces pombe
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL16192
6 Samples
Download data: SGR
Series
Accession:
GSE135160
ID:
200135160
2.

Cryptic introns in lncRNAs recruit conserved Pir2/ARS2 protein to promote gene repression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Schizosaccharomyces pombe
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other; Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL20584 GPL16192
11 Samples
Download data: BEDGRAPH, FPKM_TRACKING, SGR
Series
Accession:
GSE135161
ID:
200135161
3.

Cryptic introns in lncRNAs recruit conserved Pir2/ARS2 protein to promote gene repression [RNA-Seq]

(Submitter supplied) Long non-coding RNAs (lncRNAs) dynamically regulate gene expression during development and in response to environmental conditions. In S. pombe, lncRNAs repress the expression of nearby genes via a mechanism involving silencing effector proteins. In this study, we find that invasion of a lncRNA into the neighboring gene results in inclusion of a cryptic intron that is required for its repressive activity. more...
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16192
2 Samples
Download data: FPKM_TRACKING
Series
Accession:
GSE135159
ID:
200135159
4.

Cryptic introns in lncRNAs recruit conserved Pir2/ARS2 protein to promote gene repression [RIP-seq]

(Submitter supplied) Long non-coding RNAs (lncRNAs) dynamically regulate gene expression during development and in response to environmental conditions. In S. pombe, lncRNAs repress the expression of nearby genes via a mechanism involving silencing effector proteins. In this study, we find that invasion of a lncRNA into the neighboring gene results in inclusion of a cryptic intron that is required for its repressive activity. more...
Organism:
Schizosaccharomyces pombe
Type:
Other
Platform:
GPL20584
2 Samples
Download data: BEDGRAPH
Series
Accession:
GSE135158
ID:
200135158
5.

Cryptic introns in lncRNAs recruit conserved Pir2/ARS2 protein to promote gene repression [ChIP-seq]

(Submitter supplied) Long non-coding RNAs (lncRNAs) dynamically regulate gene expression during development and in response to environmental conditions. In S. pombe, lncRNAs repress the expression of nearby genes via a mechanism involving silencing effector proteins. In this study, we find that invasion of a lncRNA into the neighboring gene results in inclusion of a cryptic intron that is required for its repressive activity. more...
Organism:
Schizosaccharomyces pombe
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20584
1 Sample
Download data: BEDGRAPH
Series
Accession:
GSE135157
ID:
200135157
6.

Expression profiling and ChIP-chip of Schizosaccharomyces pombe strains wildtype, erh1∆, and ccr4∆

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL6503 GPL16192
21 Samples
Download data: FPKM_TRACKING, TXT
Series
Accession:
GSE76114
ID:
200076114
7.

Expression profiling of fission yeast strains: wild-type, erh1∆, and ccr4∆

(Submitter supplied) We report gene expression profiling in the fission yeast Schizosaccharomyces pombe. We performed high-throughput sequencing of RNA isolated from wild-type, erh1∆, and ccr4∆ strains. We find that many meiotic gene containing degradation sequence DSR are expressed in vegetative erh1∆, while these meiotic mRNAs do not increase in ccr4∆, indicating that Erh1 and Ccr4 target different set of genes during vegetative growth.
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16192
5 Samples
Download data: FPKM_TRACKING
Series
Accession:
GSE76112
ID:
200076112
8.

The fission yeast Schizosaccharomyces pombe: H3K9me2, Erh1-GFP and CFP-Mmi1 ChIP-chip

(Submitter supplied) ChIP-chip analyses of H3K9me2 (in WT, erh1∆, mmi1∆ and ccr4∆), Erh1-GFP (in WT and mmi1∆) and CFP-Mmi1 (in WT)
Organism:
Schizosaccharomyces pombe
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL6503
16 Samples
Download data: TXT
Series
Accession:
GSE76111
ID:
200076111
9.

Temperature shift time-course of Pre-mRNA splicing factor mutants

(Submitter supplied) Measurement of expression levels as a time course after shifting temperature-sensitive splicing factor mutant cells from 23C to 37C. Analysis of WT SS330, prp17 null, prp17-1 and prp22-1 cells. Samples were analyzed at 0, 5, 15, 30, 60 and 120 min. Keywords = pre-mRNA splicing Keywords = time course Keywords = intron Keywords: time-course
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Dataset:
GDS759
Platform:
GPL1458
24 Samples
Download data
Series
Accession:
GSE1784
ID:
200001784
10.
Full record GDS759

Pre-mRNA splicing factor mutants at restrictive temperature: time course

Analysis of gene expression in temperature sensitive pre-mRNA splicing factor mutants prp17 null, prp17-1, and prp22-1 at various time points following a shift from the permissive temperature of 23°C to the restrictive temperature of 37°C. Results identify substrates of Prp17p and Prp22p.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array, log ratio, 4 genotype/variation, 2 temperature, 6 time sets
Platform:
GPL1458
Series:
GSE1784
24 Samples
Download data
DataSet
Accession:
GDS759
ID:
759
11.

Genome-wide data of RNAs associated to Mmi1 in wild type Schizosaccharomyces pombe cells

(Submitter supplied) Mmi1 is a YTH domain containing protein. We used Solexa Deep Sequencing to identify the mRNas and lncRNAs specifically associated to Mmi1.
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL13988
4 Samples
Download data: TXT
Series
Accession:
GSE90688
ID:
200090688
12.

CPF is required for heterochromatin assembly and gene silencing

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL20584 GPL16192
23 Samples
Download data: BEDGRAPH, BW, TXT
Series
Accession:
GSE123144
ID:
200123144
13.

CPF is required for heterochromatin assembly and gene silencing [RNA-seq]

(Submitter supplied) RNA sequencing in Schizosaccharomyces pombe
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20584
4 Samples
Download data: TXT
Series
Accession:
GSE123138
ID:
200123138
14.

CPF is required for heterochromatin assembly and gene silencing [ChIP-seq]

(Submitter supplied) Mapping of H3K9me2, 3' RNA processing and termination factors, and terminating RNA polymerase II in Schizosaccharomyces pombe
Organism:
Schizosaccharomyces pombe
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL20584 GPL16192
19 Samples
Download data: BEDGRAPH, BW
Series
Accession:
GSE123137
ID:
200123137
15.

Accumulation of RNA on chromatin disrupts heterochromatic silencing

(Submitter supplied) Long non-coding RNAs (lncRNAs) play a conserved role in regulating gene expression, chromatin dynamics and cell differentiation. They serve as a platform for RNA interference (RNAi)-mediated heterochromatin formation or DNA methylation in many eukaryotic organisms. We found in Schizosaccharomyces pombe, that heterochromatin is lost at transcribed regions in absence of RNA degradation, although establishment is not affected. more...
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL9453 GPL22681
70 Samples
Download data: TDF
Series
Accession:
GSE94129
ID:
200094129
16.

The histone variant H2A.Z promotes splicing of weak introns

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by array; Other; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL21587 GPL17225
32 Samples
Download data: BEDGRAPH, GPR
Series
Accession:
GSE97984
ID:
200097984
17.

The histone variant H2A.Z promotes splicing of weak introns (array)

(Submitter supplied) Multiple lines of evidence implicate chromatin in the regulation of pre-mRNA splicing. However, the influence of chromatin factors on co-transcriptional splice-site usage remains unclear. Here we investigated the function of the highly conserved histone variant H2A.Z in pre-mRNA splicing using the intron-rich model yeast, Schizosaccharomyces pombe. Using Epistatic Mini-Array Profiles (EMAPs) to survey the genetic interaction landscape of the Swr1 nucleosome remodeling complex, which deposits H2A.Z, we uncovered evidence for functional interactions with components of the spliceosome. more...
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by array; Other
Platform:
GPL21587
30 Samples
Download data: GPR
Series
Accession:
GSE97983
ID:
200097983
18.

The histone variant H2A.Z promotes splicing of weak introns (ChIP-Seq)

(Submitter supplied) Multiple lines of evidence implicate chromatin in the regulation of pre-mRNA splicing. However, the influence of chromatin factors on co-transcriptional splice-site usage remains unclear. Here we investigated the function of the highly conserved histone variant H2A.Z in pre-mRNA splicing using the intron-rich model yeast, Schizosaccharomyces pombe. Using Epistatic Mini-Array Profiles (EMAPs) to survey the genetic interaction landscape of the Swr1 nucleosome remodeling complex, which deposits H2A.Z, we uncovered evidence for functional interactions with components of the spliceosome. more...
Organism:
Schizosaccharomyces pombe
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17225
2 Samples
Download data: BEDGRAPH
Series
Accession:
GSE97982
ID:
200097982
19.

Identification of transcripts simultaneously bound by Mmi1 and Mei2

(Submitter supplied) We determined the repertoire of transcripts simultaneously bound by Mmi1 and Mei2 through sequential immunoprecipitations followed by high-throughput sequencing of associated RNAs (seqRIP-seq)
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20584
8 Samples
Download data: TXT
Series
Accession:
GSE152383
ID:
200152383
20.

Expression profiling of the wild type, mot2∆, mamRNA∆ and mot2∆ mamRNA∆ strains

(Submitter supplied) Transcriptome analyses of wild type, mot2∆, mamRNA∆ and mot2∆ mamRNA∆ strains. We determined the role of mamRNA in the accumulation of Mmi1-targeted transcripts observed in mot2∆ cells.
Organism:
Schizosaccharomyces pombe
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23689
8 Samples
Download data: TXT
Series
Accession:
GSE152159
ID:
200152159
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