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Links from GEO DataSets

Items: 14

1.

PML is a ROS sensor activating p53 upon oxidative stress

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL17692 GPL11533 GPL17400
30 Samples
Download data: CEL
Series
Accession:
GSE100617
ID:
200100617
2.

PML is a ROS sensor activating p53 upon oxidative stress

(Submitter supplied) PML nuclear bodies (NBs) recruit partner proteins -including p53 and its regulators- controlling their abundance or function. Investigating arsenic sensitivity of acute promyelocytic leukemia, we proposed that PML oxidation promotes NB-biogenesis. Yet, physiological links between PML and oxidative stress response in vivo remain unexplored. Here we identify PML as a reactive oxygen species (ROS) sensor. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17692
8 Samples
Download data: CEL
Series
Accession:
GSE103642
ID:
200103642
3.

Gene expression profiling of Pml wt and Pml KO mice liver with acetaminophen (apap) overdose (300mg/kg) i.p.

(Submitter supplied) The Pml gene is essential to the formation of PML nuclear bodies, domains which have been associated with various functions such as apoptosis/senescence, DNA repair and cell proliferation( Lallemand-Breitenbach 2010). PML-NBs formation is regulated by cellular stress including oxidative stress(Jeanne 2010, de The 2012). To investigate the role of PML in ROS response in vivo, we analyse the expression difference to the acetaminophen toxicity, which is initiated by ROS, in Pml wt and Pml KO mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11533
12 Samples
Download data: CEL
Series
Accession:
GSE100616
ID:
200100616
4.

Gene expression profiling of Pml wt and Pml KO mice liver after fasted 6h

(Submitter supplied) The Pml gene is essential to the formation of PML nuclear bodies, domains which have been associated with various functions such as apoptosis/senescence, DNA repair and cell proliferation( Lallemand-Breitenbach 2010). PML-NBs formation is regulated by cellular stress including oxidative stress(Jeanne 2010, de The 2012). To investigate the role of PML in ROS response in vivo, we analyse the expression difference betweem Pml wt and Pml KO under fasted condition, which easily up-regulate ROS in BALB/cByJ background
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17400
10 Samples
Download data: CEL
Series
Accession:
GSE100615
ID:
200100615
5.

Profiling of APEX-NLS and APEX-PMLca associated regions

(Submitter supplied) To address specificity of ALaP-seq for PMLwt, we performed genome-wide profiling of genomic regions associated with NLS-APEX or PMLca-APEX. Cells were treated with H2O2 to trigger labeling of chromatin with biotin (H2O2+). Experimental negative control for PMLca (H2O2-), where the H2O2 treatment was omitted, was also analyzed.
Organism:
Mus musculus
Type:
Other
Platform:
GPL24247
5 Samples
Download data: BIGWIG
Series
Accession:
GSE143362
ID:
200143362
6.

ALaP-seq and RNA-seq analyses of paraquat treated mESCs

(Submitter supplied) To address the roles of PML bodies in transcription under stress condition, we performed ALaP-seq and RNA-seq with paraquat treated mESCs.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL24247
6 Samples
Download data: BIGWIG, TXT
Series
Accession:
GSE143361
ID:
200143361
7.

Dissecting roles of PML bodies by genome-wide profiling of PML body-associated regions

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL17021 GPL21493 GPL24247
43 Samples
Download data
Series
Accession:
GSE135563
ID:
200135563
8.

ChIP-seq analysis of wild-type and PML KO mESCs

(Submitter supplied) Promyelocytic leukemia (PML) body is a phase-separated nuclear structure composed of various proteins including several chromatin regulators, and physically associates with chromatin, implying its crucial roles for particular genome functions. To investigate roles of PML bodies in transcriptional regulation, we conducted ChIP-seq analysis for histone modifications, including H3K4me3, H3K27ac, H3K27me3, and H3K9ac with wild-type and PML knockout mESCs.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21493
18 Samples
Download data: BW
Series
Accession:
GSE135562
ID:
200135562
9.

ATAC-seq analyses with wild-type and PML KO mESCs

(Submitter supplied) Promyelocytic leukemia (PML) body is a phase-separated nuclear structure composed of various proteins including several chromatin regulators, and physically associates with chromatin, implying its crucial roles for particular genome functions. To investigate functional roles of PML bodies in chromatin organization, we conducted ATAC-seq with wild-type and PML KO mESCs.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21493
4 Samples
Download data: BW
Series
Accession:
GSE135561
ID:
200135561
10.

Profiling of PML-body associated regions

(Submitter supplied) The promyelocytic leukemia (PML) body is a phase-separated nuclear structure composed of various proteins including several chromatin regulators, and physically associates with chromatin. To address functional roles of the PML-chromatin association, we conducted genome-wide profiling of PML body-associated regions.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21493
4 Samples
Download data: BED, BW
Series
Accession:
GSE135560
ID:
200135560
11.

RNA-seq analyses of wild-type and PML KO mESCs

(Submitter supplied) Promyelocytic leukemia (PML) body is a phase-separated nuclear structure composed of various proteins including several chromatin regulators, and physically associates with chromatin. To address roles of PML bodies in transcriptional regulation, we performed RNA-seq analyses with wild-type and PMK knockout mESCs
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: TDF, XLSX
Series
Accession:
GSE135557
ID:
200135557
12.

Expression data from xenograft in BALB/c 6-wk-old nude mice with PC3 prostate cancer cells stably expressing PML or a vector control after treatment of the mice with palbociclib

(Submitter supplied) Expression data from xenograft in BALB/c 6-wk-old nude mice with PC3 prostate cancer cells stably expressing PML or a vector control after treatment of the mice with palbociclib (100mg/kg/day diluted in sodium lactate 50mM pH4 given by gavage) during 5 consecutive days PML plays a role in the senescence tumor suppressor response of normal cells to oncogenic stress. PML also mediates therapy-induced senescence in acute promyelocytic leukemia cells after treatment with retinoic acid. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE70923
ID:
200070923
13.

H2AX controls motor learning and response to oxidative stress

(Submitter supplied) ATM drives DNA repair through rapid phosphorylation of the histone variant H2AX. Similarities between ATM and H2AX are evident in the phenotypes of their knockout mouse models, but the role of H2AX in the brain remains obscure. Here, we provide the first evidence that H2AX loss leads to neurobehavioral deficits. H2AX regulates proper response to oxidative stress through Nrf2-transcriptional targets and treatment with antioxidant ameliorates the neurobehavioral deficits.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
6 Samples
Download data: CEL
Series
Accession:
GSE102548
ID:
200102548
14.

Alterations of redox and iron metabolism accompany development of HIV latency

(Submitter supplied) Metabolic alterations, such as oxidative stress, are hallmarks of HIV-1 infection. However, their influence on the development of viral latency, and thus on HIV-1 persistence during antiretroviral therapy (ART), have just begun to be explored. We analyzed omics profiles of in-vitro and in-vivo models of infection by HIV-1 and its simian homolog SIVmac. We found that cells survive retroviral replication by upregulating antioxidant pathways and intertwined iron import pathways. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
24 Samples
Download data: XLSX
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