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Links from GEO DataSets

Items: 20

1.

Targets of the transcription factor Brachyury in differentiating mouse ES cells

(Submitter supplied) Brachyury (or T) is expressed in the primitive streak, tailbud and notochord of the early mouse embryo (Herrmann et al., 1990; Wilkinson et al., 1990). It plays a key role in early development: mouse embryos lacking functional Brachyury protein fail to gastrulate properly, do not form a differentiated notochord, and lack structures posterior to somite seven (Chesley, 1935; Dobrovolskaïa-Zavadskaïa, 1927; Naiche et al., 2005; Wilson et al., 1995; Wilson et al., 1993; Yanagisawa et al., 1981) We apply a ChIP-on-chip approach to identify targets of Brachyury during mouse ES cell differentiation. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL4129 GPL4128
4 Samples
Download data: TXT
Series
Accession:
GSE16646
ID:
200016646
2.

UTX regulated genes in mouse embryonic stem cells

(Submitter supplied) UTX gene is localized on the X chromosome, identified as a demethylase on histone H3 lysine 27.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5465
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE35415
ID:
200035415
3.
Full record GDS5465

UTX deficiency effect on embryonic stem cells

Analysis of embryonic stem cells lacking UTX. UTX is a histone H3K27 demethylase that belongs to the the family of JmjC domain-containing proteins. Results provide insight into the role of UTX in embryonic stem cell differentiation.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL1261
Series:
GSE35415
4 Samples
Download data: CEL
4.

A 37 kb region upstream of Brachyury comprising a notochord enhancer is essential for notochord and tail development

(Submitter supplied) Genetic dissection of the mouse Brachyury locus identified a notochord enhancer and predicts additional control elements essential for trunk and tail development of the mouse embryo.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21103
1 Sample
Download data: BW
Series
Accession:
GSE179665
ID:
200179665
5.

A mesodermal gene regulatory network directed by zebrafish No tail

(Submitter supplied) Using chromatin immunoprecipitation combined with microarrays we have identified targets of No tail (Ntl), a zebrafish Brachyury ortholog that plays a central role in mesoderm formation. We show that Ntl regulates a downstream network of other transcription factors and identify an in vivo Ntl binding site that resembles the consensus T-box binding site (TBS) previously identified by in vitro studies. more...
Organism:
Danio rerio
Type:
Genome binding/occupancy profiling by genome tiling array
9 related Platforms
27 Samples
Download data: GPR
Series
Accession:
GSE12331
ID:
200012331
6.

Genome wide maps of H3K4me3, H3K27me3 and H3K27ac in Brachyury mutants and RNA-seq data of Brachyury mutants

(Submitter supplied) The transcription factor BRACHYURY is the founding member of the T-box family of proteins. A conserved residue (Y88 in BRACHYURY) was previously suggested to be important for interaction with KDM proteins that demethylate H3K27me3. We generated Brachyury mutant mouse embryonic stem cell (ESC) lines. For a wild type control (Thet) we derived an embryonic stem cell line from blastocysts, containing a single wild type copy of the Brachyury locus (T +/2J; 2J is a large genomic deletion of the entire Brachyury locus). more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL17021
12 Samples
Download data: BW, XLSX
Series
Accession:
GSE94142
ID:
200094142
7.

BRACHYURY orchestrates distinct mesoderm and endoderm gene regulatory networks in differentiating human embryonic stem cells

(Submitter supplied) The transcription factor BRACHYURY (T, BRA) is one of the first markers of gastrulation and lineage specification in mammals. Despite its wide use and importance in stem cell and developmental biology, its genomic targets are largely unknown. Here, we used differentiated human embryonic stem cells to study the role of BRA in Bmp4-induced mesoderm and Activin-induced endoderm progenitors by ChIP-seq. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9115
6 Samples
Download data: BED, BW
Series
Accession:
GSE60606
ID:
200060606
8.

Illumina microarray experiment on LSD1 deletion ES cell with Lsd1Lox/Δ3 and Lsd1Δ3/Δ3

(Submitter supplied) Lysine specific demethylase 1 (LSD1), which demethylates mono- and di- methylated histone H3-Lys4 as part of a complex including CoREST and histone deacetylases (HDAC), is essential for embryonic development in the mouse beyond e6.5 days. Here, we demonstrate that LSD1 expression and therefore function, is restricted to the epiblast of the post- implantation embryo. Conditional deletion of LSD1 in mouse embryonic stem (ES) cells, in vitro counterpart of the epiblast, revealed a reduction in CoREST protein, a subsequent decrease in associated HDAC activity and a global increase in Histone H3 Lys56 acetylation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
6 Samples
Download data: TXT
Series
Accession:
GSE21131
ID:
200021131
9.

Transcriptional Activation by Oct4 Is Sufficient for the Maintenance and Induction of Pluripotency

(Submitter supplied) Oct4 is an essential regulator of embryonic stem (ES) cell pluripotency in vivo and in vitro, as well as a key mediator of the reprogramming of somatic cells to form induced pluriopotent stem (iPS) cells. It is not known whether activation and/or repression of specific genes by Oct4 is relevant to these functions. Here we show that fusion proteins containing the coding sequence of Oct4 or Xlpou91 (the Xenopus homologue of Oct4) fused to activating regions, but not those fused to repressing regions, behave as Oct4, suppressing differentiation and promoting maintenance of undifferentiated phenotypes in vivo and in vitro. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6867
18 Samples
Download data: TXT
Series
Accession:
GSE24563
ID:
200024563
10.

The molecular basis of specific functions of Brachyury and Eomes for mesoderm and endoderm lineage specification

(Submitter supplied) The Tbx factors Eomesodermin (Eomes) and Brachyury instruct endoderm and mesoderm specification. Both Tbx factors have common large overlap in chromatin binding sites, however their embryonic phenotypes of mutants largely differ. In this study, we delineate the distinct binding patterns and gene target sets of Eomes and Brachyury providing a molecular model of distinct fate specification programs.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL19057 GPL24247
20 Samples
Download data: BED, BIGWIG, TXT
Series
Accession:
GSE194192
ID:
200194192
11.

Expression profiling of Ciona intestinalis neurula and mid-tailbud stage embryos expressing altered forms of the transcription factor Ci-Tbx2/3 in the notochord

(Submitter supplied) Despite being found in the notochord of several chordates, the roles of the Tbx2 subfamily of T-box transcription factors in the development of this tissue remain largely unknown. We explored the targets of the only Tbx2 subfamily member in Ciona intestinalis, Ci-Tbx2/3, by expressing mutant forms of the transcriptional regulator using the Ci-Bra promoter region. We produced a dominant interfering version of Ci-Tbx2/3 (Tbx2/3DBD) through expression of a truncated version consisting only of its DNA-binding domain (DBD) and a constitutive activator form by attaching the T-box of Ci-Tbx2/3 to the VP16 transactivation domain (Tbx2/3VP16). more...
Organism:
Ciona intestinalis
Type:
Expression profiling by array
Platform:
GPL15657
17 Samples
Download data: CEL
Series
Accession:
GSE42267
ID:
200042267
12.

The PR/SET domain Zinc finger protein Prdm4 regulates gene expression in ES cells but plays a non-essential role in the developing mouse embryo.

(Submitter supplied) ChIP-seq using anti-GFP antibody to map genomic binding of Prdm4-EGFP in stably transfected mouse embryonic stem cells
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
8 Samples
Download data: BED, WIG
Series
Accession:
GSE48372
ID:
200048372
13.

Expression analysis of Prdm4 mutant and overexpressing mouse embryonic stem cells

(Submitter supplied) Expression profiling of wild-type, Prdm4 null and Prdm4-EGFP overexpressing mouse embryonic stem cells using Illumina whole genome V2 arrays. The hypothesis tested was that Prdm4 regulates gene expression consistant with Prdm4 genomic binding identified by ChIP-seq
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
16 Samples
Download data: TXT
Series
Accession:
GSE46308
ID:
200046308
14.

Brachyury controls Ciona notochord fate as part of a feedforward network

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Ciona robusta
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL23563 GPL29327
42 Samples
Download data
Series
Accession:
GSE160548
ID:
200160548
15.

Brachyury controls Ciona notochord fate as part of a feedforward network [IV]

(Submitter supplied) The notochord is a defining feature of the chordates. The transcription factor Brachyury (Bra) is a key regulator of notochord fate but here we show that it is not a unitary master regulator in the model chordate Ciona. Ectopic Bra expression only partially reprograms other cell types to a notochord-like transcriptional profile and a subset of notochord-enriched genes are unaffected by CRISPR Bra disruption. more...
Organism:
Ciona robusta
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29327
15 Samples
Download data: XLSX
Series
Accession:
GSE160547
ID:
200160547
16.

Brachyury controls Ciona notochord fate as part of a feedforward network [III]

(Submitter supplied) The notochord is a defining feature of the chordates. The transcription factor Brachyury (Bra) is a key regulator of notochord fate but here we show that it is not a unitary master regulator in the model chordate Ciona. Ectopic Bra expression only partially reprograms other cell types to a notochord-like transcriptional profile and a subset of notochord-enriched genes are unaffected by CRISPR Bra disruption. more...
Organism:
Ciona robusta
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29327
12 Samples
Download data: XLSX
Series
Accession:
GSE160546
ID:
200160546
17.

Brachyury controls Ciona notochord fate as part of a feedforward network [II]

(Submitter supplied) The notochord is a defining feature of the chordates. The transcription factor Brachyury (Bra) is a key regulator of notochord fate but here we show that it is not a unitary master regulator in the model chordate Ciona. Ectopic Bra expression only partially reprograms other cell types to a notochord-like transcriptional profile and a subset of notochord-enriched genes are unaffected by CRISPR Bra disruption. more...
Organism:
Ciona robusta
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29327
6 Samples
Download data: XLSX
Series
Accession:
GSE160545
ID:
200160545
18.

Brachyury controls Ciona notochord fate as part of a feedforward network [I]

(Submitter supplied) The notochord is a defining feature of the chordates. The transcription factor Brachyury (Bra) is a key regulator of notochord fate but here we show that it is not a unitary master regulator in the model chordate Ciona. Ectopic Bra expression only partially reprograms other cell types to a notochord-like transcriptional profile and a subset of notochord-enriched genes are unaffected by CRISPR Bra disruption. more...
Organism:
Ciona robusta
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23563
9 Samples
Download data: XLSX
Series
Accession:
GSE160544
ID:
200160544
19.

Cdx and T Brachyury co-activate growth signaling in the embryonic axial progenitor niche.

(Submitter supplied) In vertebrate embryos, anterior tissues are generated early, followed by the other axial structures that emerge sequentially from a posterior growth zone. The genetic network driving posterior axial elongation in mice, and its disturbance in mutants with posterior truncation are not yet fully understood. We show that the combined expression of Cdx2 and T Brachyury is essential to establish the core signature of posterior axial progenitors. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
Platform:
GPL19057
55 Samples
Download data: BED, BW, CSV, WIG
Series
Accession:
GSE84899
ID:
200084899
20.

Distinct developmental ground states of different epiblast stem cell lines determine pluripotency features

(Submitter supplied) Epiblast stem cells (EpiSC) are pluripotent stem cells derived from mouse postimplantation embryos between E5.5 to E7.5, a time window in which gastrulation commences. Therefore, EpiSC represent a valuable tool for studying mammalian postimplantation development in vitro. Beyond their pluripotent features, EpiSC can also be reprogrammed into a mouse embryonic stem cell-like (mESC) state. Published reports showed that EpiSC reversion requires transcription factor overexpression, while others suggest that applying stringent mESC culture conditions alone was sufficient to revert EpiSC to mESC-like cells. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
7 Samples
Download data: TXT
Series
Accession:
GSE28270
ID:
200028270
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