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Links from GEO DataSets

Items: 20

1.

SIX6 knockdown in Jurkat-Cas9 T-ALL cell line

(Submitter supplied) T cell acute lymphoblastic leukemia (T-ALL) is a hematological malignancy strongly affected by the abnormal activity of transcription factors. Here we report a high expression of developmental transcription factor SIX6 in TAL1 subtype of T-ALL. Our data indicates that this high expression is directly regulated by binding of TAL1 and GATA3 transcription factors into an upstream enhancer element. We also looked into the potential targets of SIX6 in T-ALL and Crispr-cas9 mediated knockout of SIX6 in Jurkat cells caused significant changes in the expression of multiple genes, including genes related to mTOR signaling. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: TXT
Series
Accession:
GSE148658
ID:
200148658
2.

TAL1 regulated miRNAs

(Submitter supplied) miRNA profiling of Jurkat T-ALL cells after knockdown with two control shRNAs and two shRNAs targeting TAL1 to identify miRNAs that are regulated by TAL1
Organism:
human gammaherpesvirus 4; JC polyomavirus; Human gammaherpesvirus 8; Mus musculus cytomegalovirus 2; Betapolyomavirus macacae; Homo sapiens; Murid gammaherpesvirus 4; Betapolyomavirus hominis; Mus musculus; Human alphaherpesvirus 1; Human betaherpesvirus 5; Human immunodeficiency virus 1; Rattus norvegicus; Human alphaherpesvirus 2; Merkel cell polyomavirus
Type:
Non-coding RNA profiling by array
Platform:
GPL11432
8 Samples
Download data: TXT
Series
Accession:
GSE46957
ID:
200046957
3.

Chromatin marks and RNA Pol II in human hematopoietic stem and progenitor cells

(Submitter supplied) The transcriptional status of genes can be determined from the enrichment pattern of RNA polymerase at the transcription start site (TSS) and across the body of the gene. Active elongating genes are enriched for H3K79me2, and Polycomb paused genes are marked by H3K27me3.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9115
4 Samples
Download data: TXT, WIG
Series
Accession:
GSE26015
ID:
200026015
4.

Core transcriptional regulatory circuit controlled by the tal1 complex in human t-cell acute lymphoblastic leukemia (Subseries)

(Submitter supplied) The oncogenic transcription factor TAL1/SCL is aberrantly overexpressed in over 40% of cases of T-cell acute lymphoblastic leukemia (T-ALL), emphasizing the importance of the TAL1-regulated transcriptional program in the molecular pathogenesis of T-ALL. Here we identify the core transcriptional regulatory circuit controlled by TAL1 and its regulatory partners HEB, E2A, GATA3, ETS1 and RUNX1 in T-ALL cells. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
22 Samples
Download data: WIG, YLF
Series
Accession:
GSE33850
ID:
200033850
5.

Core transcriptional regulatory circuit controlled by the TAL1 complex in human T-cell acute lymphoblastic leukemia

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL11154 GPL9115 GPL13232
64 Samples
Download data: CEL, WIG, YLF
Series
Accession:
GSE29181
ID:
200029181
6.

ChIP-Seq of TAL1 and its regulatory partners in T-ALL cells

(Submitter supplied) The oncogenic transcription factor TAL1/SCL is aberrantly expressed in over 40% of cases of T-cell acute lymphoblastic leukemia (T-ALL), emphasizing its importance in the molecular pathogenesis of T-ALL. Here we identify the core transcriptional regulatory circuit controlled by TAL1 and its regulatory partners HEB, E2A, LMO1, LMO2, GATA3 and RUNX1 in T-ALL cells. We show that TAL1 forms an interconnected auto-regulatory loop with its partners, and that the TAL1 complex directly activates the MYB oncogene, forming a feed-forward positive regulatory loop that further promotes the TAL1-regulated oncogenic program. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9115
10 Samples
Download data: WIG, YLF
Series
Accession:
GSE29180
ID:
200029180
7.

Identification of differentially expressed genes upon shRNA knockdown of TAL1 and its regulatory partners in T-ALL cells (Jurkat)

(Submitter supplied) The oncogenic transcription factor TAL1/SCL is aberrantly overexpressed in over 40% of cases of T-cell acute lymphoblastic leukemia (T-ALL), emphasizing the importance of the TAL1-regulated transcriptional program in the molecular pathogenesis of T-ALL. Here we identify the core transcriptional regulatory circuit controlled by TAL1 and its regulatory partners HEB, E2A, GATA3, ETS1 and RUNX1 in T-ALL cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13232
32 Samples
Download data: CEL
Series
Accession:
GSE29179
ID:
200029179
8.

Gene expression profile in human T-cell acute lymphoblastic leukemia (T-ALL) cell lines

(Submitter supplied) We performed microarray gene expression profiling in 16 T-ALL cell lines
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
16 Samples
Download data: CEL
Series
Accession:
GSE90138
ID:
200090138
9.

RNA-seq analysis in Jurkat cells

(Submitter supplied) RNA-seq analysis was performed in Jurkat cells (T-cell lymphoblastic leukemia cell line).
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
1 Sample
Download data: BW
10.

T-cell ALL in response to TAL1-KD, UTX-KD, and GSKJ4 treatment

(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; Third-party reanalysis
Platform:
GPL11154
17 Samples
Download data: BED, BW
Series
Accession:
GSE72300
ID:
200072300
11.

Gene expression in TAL1-driven T-cell ALL in response to TAL1-KD, UTX-KD, and GSKJ4 treatment

(Submitter supplied) T-cell Acute Lymphoblastic Leukemia (T-ALL) is a heterogeneous group of hematological tumors composed of distinct subtypes that vary in their genetic abnormalities, gene expression signatures and prognoses. However, it remains unclear whether T-ALL subtypes differ at the functional level, and as such T-ALL treatments are uniformly applied across subtypes leading to variable responses between patients. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
12 Samples
Download data: R, TXT
12.

H3K27 methylation changes in Jurkat cells in response to TAL1-KD

(Submitter supplied) T-cell Acute Lymphoblastic Leukemia (T-ALL) is a heterogeneous group of hematological tumors composed of distinct subtypes that vary in their genetic abnormalities, gene expression signatures and prognoses. However, it remains unclear whether T-ALL subtypes differ at the functional level, and as such T-ALL treatments are uniformly applied across subtypes leading to variable responses between patients. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
3 Samples
Download data: BED
Series
Accession:
GSE72298
ID:
200072298
13.

UTX inhibition as selective epigenetic therapy against TAL1-driven T cell acute lymphoblastic leukemia

(Submitter supplied) We performed ChIP-Seq in Jurkat T-ALL cells to identify UTX binding sites across the genome. We then compared UTX binding sites (this study) with TAL1 binding sites (Data from Palii, 2011 GSE25000), and found a high degree of overlap between TAL1 and UTX in Jurkat T-All cells. Indeed, over 80% of TAL1 binding sites overlap with UTX.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Third-party reanalysis
Platform:
GPL11154
2 Samples
Download data: BED, BW
Series
Accession:
GSE64832
ID:
200064832
14.

Differential genomic targeting of the transcription factor TAL1 in alternate hematopoietic lineages

(Submitter supplied) TAL1/SCL is a master regulator of hematopoiesis whose expression promotes opposite outcomes depending on the cell type - differentiation in the erythroid lineage or oncogenesis in the T-cell lineage. Here we used a combination of ChIP-sequencing and gene expression profiling to compare the function of TAL1 in normal erythroid and leukemic T-cells. Analysis of the genome-wide binding properties of TAL1 in these two hematopoietic lineages revealed new insight into the mechanism by which transcription factors select their binding sites in alternate lineages. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9052
3 Samples
Download data: BED, MAP
Series
Accession:
GSE25000
ID:
200025000
15.

TAL1 hijacks MYCN enhancer that induces MYCN expression and dependence on mevalonate pathway in T-cell acute lymphoblastic leukemia

(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
Platforms:
GPL28038 GPL24676
34 Samples
Download data: BED, BEDPE, BW, NARROWPEAK, TXT
Series
Accession:
GSE231965
ID:
200231965
16.

Genome wide analysis of binding regions for MYC, MYCN and various histone modifications using Cut&Run

(Submitter supplied) Cut&Run analysis was performed in RPMI-8402 cells to analyze binding regions of MYC, MYCN and various histone modifications in normal culture conditions
Organism:
Homo sapiens
Type:
Other
Platform:
GPL24676
10 Samples
Download data: BED, BW
Series
Accession:
GSE231963
ID:
200231963
17.

RNA-seq analysis in RPMI-8402 cells after knockout of MYC and MYCN

(Submitter supplied) RNA-seq analysis was performed in a RPMI-8402 T-ALL cell stably expressing Cas9 aafter knockout of both MYC and MYCN
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28038
6 Samples
Download data: TXT
Series
Accession:
GSE231962
ID:
200231962
18.

RNA-seq analysis in RPMI-8402 cells after knockout of MYC

(Submitter supplied) RNA-seq analysis was performed in a RPMI-8402 T-ALL cell stably expressing Cas9 after knockout of MYC
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28038
6 Samples
Download data: TXT
Series
Accession:
GSE231960
ID:
200231960
19.

RNA-seq analysis in RPMI-8402 cells after knockout of MYCN

(Submitter supplied) RNA-seq analysis was performed in a RPMI-8402 T-ALL cell stably expressing Cas9 after knockout of MYCN
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28038
6 Samples
Download data: TXT
Series
Accession:
GSE231959
ID:
200231959
20.

H3K27ac Hi-ChIP analysis in Jurkat and RPMI-8402 T-ALL cells

(Submitter supplied) H3K27ac Hi-ChIP analysis was performed in Jurkat and RPMI-8402 stably expressing dCAR9-KRAB after treatment with DMSO (Control) or Doxycycline to induce sgRNA expression to block MYCN enhnacer region
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL28038
4 Samples
Download data: BED, BEDPE, TXT
Series
Accession:
GSE231957
ID:
200231957
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