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Links from GEO DataSets

Items: 20

1.

Co-ordinate inhibition of autism candidate genes by topoisomerase inhibitors

(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; Expression profiling by array
5 related Platforms
70 Samples
Download data: CEL, TXT
Series
Accession:
GSE43900
ID:
200043900
2.

Co-ordinate inhibiton of autism candidate genes by topoisomerase inhibitors [array]

(Submitter supplied) Topoisomerases are necessary for the expression of neurodevelopmental genes, and are mutated in some patients with autism spectrum disorder (ASD). We have studied the effects of inhibitors of Topoisomerase 1 (Top1) and Topoisomerase 2 (Top2) enzymes on mouse cortical neurons. We find that topoisomerases selectively inhibit long genes (>100kb), with little effect on all other gene expression. Using ChIPseq against RNA Polymerase II (Pol2) we show that the Top1 inhibitor topotecan blocks transcriptional elongation of long genes specifically. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL1261 GPL17400 GPL11533
56 Samples
Download data: CEL
Series
Accession:
GSE43899
ID:
200043899
3.

Co-ordinate inhibition of autism candidate genes by topoisomerase inhibitors [Seq]

(Submitter supplied) Topoisomerases are necessary for the expression of neurodevelopmental genes, and are mutated in some patients with autism spectrum disorder (ASD). We have studied the effects of inhibitors of Topoisomerase 1 (Top1) and Topoisomerase 2 (Top2) enzymes on mouse cortical neurons. We find that topoisomerases selectively inhibit long genes (>100kb), with little effect on all other gene expression. Using ChIPseq against RNA Polymerase II (Pol2) we show that the Top1 inhibitor topotecan blocks transcriptional elongation of long genes specifically. more...
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL13112 GPL11154
14 Samples
Download data: TXT
Series
Accession:
GSE43526
ID:
200043526
4.

Topoisomerase 1 Regulates Gene Expression in Neurons through Cleavage Complex-Dependent and -Independent Mechanisms

(Submitter supplied) Topoisomerase 1 (TOP1) inhibitors, including camptothecin and topotecan, covalently trap TOP1 on DNA, creating cleavage complexes (cc’s) that must be resolved before gene transcription and DNA replication can proceed. We previously found that topotecan reduces the expression of long (>100 kb) genes and unsilences the paternal allele of Ube3a in neurons. Here, we sought to evaluate overlap between TOP1cc-dependent and -independent gene regulation in neurons. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
12 Samples
Download data: TXT
Series
Accession:
GSE79951
ID:
200079951
5.

Topoisomerase II binds nucleosome-free DNA and acts redundantly with Topoisomerase I to enhance recruitment of RNA Pol II in budding yeast

(Submitter supplied) DNA topoisomerases are known to promote transcription in prokaryotes by removing excessive DNA supercoils produced during elongation. However, it is unclear how topoisomerases in eukaryotes are recruited and function in the transcription pathway in the context of nucleosomes. To address this problem we present high-resolution genome wide maps of one of the major eukaryotic topoisomerases, Topoisomerase II (Top2) and nucleosomes in the budding yeast, Saccharomyces cerevisiae. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL4130 GPL7250
15 Samples
Download data: BAR, CEL, TSV, TXT
Series
Accession:
GSE22626
ID:
200022626
6.

Study of Topoisomerase I in human

(Submitter supplied) We report a mechanism through which the transcription machinery directly controls topoisomerase 1 (TOP1) activity to adjust DNA topology throughout the transcription cycle. By comparing TOP1 occupancy using ChIP-Seq, versus TOP1 activity using TOP1-Seq, a method reported here to map catalytically engaged TOP1, TOP1 bound at promoters was discovered to become fully active only after pause-release. This transition coupled the phosphorylation of the carboxyl-terminal-domain (CTD) of RNA polymerase II (RNAPII) with stimulation of TOP1 above its basal rate, enhancing its processivity. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL9115 GPL9520
27 Samples
Download data: TXT, WIG
Series
Accession:
GSE57628
ID:
200057628
7.

MYC assembles and stimulates topoisomerases 1 & 2 in a “topisome”

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL24676 GPL21697
37 Samples
Download data: BW
Series
Accession:
GSE181450
ID:
200181450
8.

MYC assembles and stimulates topoisomerases 1 & 2 in a “topisome” [cross-CAD-seq]

(Submitter supplied) High-intensity transcription and replication supercoil DNA to levels that can impede or halt these processes. As a potent transcription amplifier and replication accelerator, the proto-oncogene MYC must somehow manage these high levels of torsional stress. By comparing gene expression with the recruitment of topoisomerases and MYC to promoters, we surmised a direct association of MYC with Topoisomerases 1 (TOP1) and 2A (TOP2A) that was confirmed in vitro and in vivo. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24676
13 Samples
Download data: BW
Series
Accession:
GSE181449
ID:
200181449
9.

MYC assembles and stimulates topoisomerases 1 & 2 in a “topisome” [CAD-seq]

(Submitter supplied) High-intensity transcription and replication supercoil DNA to levels that can impede or halt these processes. As a potent transcription amplifier and replication accelerator, the proto-oncogene MYC must somehow manage these high levels of torsional stress. By comparing gene expression with the recruitment of topoisomerases and MYC to promoters, we surmised a direct association of MYC with Topoisomerases 1 (TOP1) and 2A (TOP2A) that was confirmed in vitro and in vivo. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21697
4 Samples
Download data: BW
Series
Accession:
GSE181448
ID:
200181448
10.

MYC assembles and stimulates topoisomerases 1 & 2 in a “topisome” [ChIP-seq]

(Submitter supplied) High-intensity transcription and replication supercoil DNA to levels that can impede or halt these processes. As a potent transcription amplifier and replication accelerator, the proto-oncogene MYC must somehow manage these high levels of torsional stress. By comparing gene expression with the recruitment of topoisomerases and MYC to promoters, we surmised a direct association of MYC with Topoisomerases 1 (TOP1) and 2A (TOP2A) that was confirmed in vitro and in vivo. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21697
20 Samples
Download data: BW, XLSX
Series
Accession:
GSE181447
ID:
200181447
11.

Genome-Wide Transcriptional Effects of the Anti-Cancer Agent Camptothecin

(Submitter supplied) The anti-cancer drug camptothecin inhibits replication and transcription by trapping DNA topoisomerase I (Top1) covalently to DNA in a “cleavable complex”. To examine the effects of camptothecin on RNA synthesis genome-wide we used Bru-Seq and show that camptothecin treatment affected transcription initiation, elongation, termination, splicing and enhancer activity. Following removal of camptothecin, transcription spread as a wave from the 5’-end of genes with no recovery of transcription apparent from RNA polymerases stalled in the body of genes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
9 Samples
Download data: TXT
12.

Saccharomyces cerevisiae cells: effect of Top2 depletion without accumulation of positive superhelical stress

(Submitter supplied) Positive DNA helical stress accumulates in vivo by the unbalanced relaxation of positive and negative DNA supercoils in Δtop1, top2ts, pGPD:TopA yeast cells. The resulting overwinding of DNA greatly diminishes overall RNA synthesis. Here we show that whereas most genes reduce their transcript levels by several fold, genes situated at less than 100 kb from the chromosomal ends (near 15% of the genome) are gradually unaffected. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL9281
6 Samples
Download data: TXT
Series
Accession:
GSE18605
ID:
200018605
13.

Saccharomyces cerevisiae cells: control vs positive supercoiling accumulation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platforms:
GPL9282 GPL9281
21 Samples
Download data: TXT
Series
Accession:
GSE18242
ID:
200018242
14.

S. cerevisiae cells: control vs positive supercoiling accumulation in absence of telomere silencing after 0 and 120 min

(Submitter supplied) Positive DNA helical stress accumulates in vivo by the unbalanced relaxation of positive and negative DNA supercoils in Δtop1, top2ts, pGPD:TopA yeast cells. The resulting overwinding of DNA greatly diminishes overall RNA synthesis. Here we show that whereas most genes reduce their transcript levels by several fold, genes situated at less than 100 kb from the chromosomal ends (near 15% of the genome) are gradually unaffected. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL9282
6 Samples
Download data: TXT
Series
Accession:
GSE18241
ID:
200018241
15.

Saccharomyces cerevisiae cells: control vs positive supercoiling accumulation after 0, 30 and 120 min

(Submitter supplied) Positive DNA helical stress accumulates in vivo by the unbalanced relaxation of positive and negative DNA supercoils in Δtop1, top2ts, pGPD:TopA yeast cells. The resulting overwinding of DNA greatly diminishes overall RNA synthesis. Here we show that whereas most genes reduce their transcript levels by several fold, genes situated at less than 100 kb from the chromosomal ends (near 15% of the genome) are gradually unaffected. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL9281
9 Samples
Download data: TXT
Series
Accession:
GSE18240
ID:
200018240
16.

GRO analysis of topoisomerase mutants

(Submitter supplied) Genomic Run-on analysis of topoisomerase mutants (top1-delta/top2ts or top2ts) has been conducted at reference temperature for wt strain and at non-permissive temperature for wt and mutant strains. Keywords: Genomic Run On
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL7871
13 Samples
Download data
Series
Accession:
GSE16673
ID:
200016673
17.

Topoisomerase 1 activity during mitotic transcription favors the transition from mitosis to G1

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Other
Platform:
GPL21697
60 Samples
Download data: BW
Series
Accession:
GSE171134
ID:
200171134
18.

Topoisomerase 1 activity during mitotic transcription favors the transition from mitosis to G1 [SLAM-seq]

(Submitter supplied) Using SLAM-seq to capture de novo synthesized polyadenylated RNAs, we quantitated changes in nascent RNA expression, as well as in total RNA expression.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL21697
12 Samples
Download data: CSV
Series
Accession:
GSE171133
ID:
200171133
19.

Topoisomerase 1 activity during mitotic transcription favors the transition from mitosis to G1 [ChIP-seq]

(Submitter supplied) By following chromatin occupancy of RNAPII and TOP1 using ChIP-seq throughout mitosis, we found that TOP1 is required for RNAPII translocation along genes. The stimulation of TOP1 activity through its interaction with RNAPII during elongation, allowed RNAPII clearance from genes in prometaphase and enabled proper chromosomal segregation. Interference with the TOP1-RNAPII interaction or acute depletion of TOP1 at the onset of mitosis impaired RNAPII spiking at promoters, which is necessary for the first pioneering round of transcription during mitotic exit, and triggered defects in the transcriptional program of the post-mitotic cells.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21697
48 Samples
Download data: BW
Series
Accession:
GSE171132
ID:
200171132
20.

DNA breaks and chromatin structural changes enhance the transcription of Autoimmune Regulator target genes

(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
16 Samples
Download data
Series
Accession:
GSE89893
ID:
200089893
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