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Series GSE140000 Query DataSets for GSE140000
Status Public on Nov 01, 2020
Title The T-box Transcription Factor Eomesodermin Governs Hemogenic Competence of Yolk Sac Mesodermal Progenitors [ChIP-Seq]
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Extra-embryonic mesoderm (ExM), the earliest cells that traverse through the primitive streak, give rise to the endothelium as well as hematopoietic progenitors in the developing yolk-sac (YS). How a specific subset of ExM becomes committed to a hematopoietic fate remains unclear. Here we report that Eomesodermin (Eomes), a T-box transcription factor, is transiently expressed in ExM progenitors that generate virtually all YS hematopoietic and endothelial cells. Using an embryonic stem cell (ESC) differentiation system, we find that Eomes activity is essential for the production of primitive erythrocytes and for the normal development of Runx1+ HE that generates the definitive hematopoietic progenitors. RNA-Seq and ATAC-Seq experiments reveal that Eomes governs the accessibility of numerous hematopoietic enhancers that SCL normally utilizes to specify primitive erythrocytes and HE in Flk-1hi/PdgfRa- hematovascular mesoderm. ChIP-seq experiments suggest that Eomes coordinates the development of hemogenic competent mesoderm in the context of Activin/Nodal and Tead-Yap signaling. Finally, single-cell- RNA-seq (scRNAseq) shows that in the absence of Eomes function diversion towards an endothelial rather than hematopoietic fate occurs after the initial specification of Flk-1+/SCL+ hematovascular mesoderm. Collectively, these experiments demonstrate that Eomes sits at the top of the transcriptional hierarchy, functioning upstream of Runx1 expression and SCL functional activity, and promotes hemogenic competence of the entire YS mesodermal lineage.
 
Overall design EoV5 ChIP-Seq occupancy profiles for one wild type and two Eo-V5 clones (A&B) from day 4 EBs, generated by deep sequencing using Illumina HiSeq4000.
 
Contributor(s) Harland LT, Simon CS, Senft AD, Costello I, Greder L, Bikoff EK, Porcher C, de Bruijn M, Robertson EJ
Citation(s) 33420489
Submission date Nov 06, 2019
Last update date Apr 06, 2021
Contact name Luke Thomas Gilbert Harland
E-mail(s) luke.harland@path.ox.ac.uk
Organization name Oxford University
Department Sir William Dunn School of Pathology
Lab Elizabeth Robertson
Street address South Parks Road
City Oxford
ZIP/Postal code OX1 3RE
Country United Kingdom
 
Platforms (1)
GPL21103 Illumina HiSeq 4000 (Mus musculus)
Samples (6)
GSM4151332 ChIP_WT_input
GSM4151333 ChIP_WT_IP
GSM4151334 ChIP_EoV5_A_input
This SubSeries is part of SuperSeries:
GSE140005 The T-box Transcription Factor Eomesodermin Governs Hemogenic Competence of Yolk Sac Mesodermal Progenitors
Relations
BioProject PRJNA587985
SRA SRP228773

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE140000_ChIP_EoV5_A.bw 899.1 Mb (ftp)(http) BW
GSE140000_ChIP_EoV5_B.bw 903.4 Mb (ftp)(http) BW
GSE140000_ChIP_WT.bw 885.2 Mb (ftp)(http) BW
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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