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Series GSE168377 Query DataSets for GSE168377
Status Public on Jan 14, 2022
Title YAP1 Drives Lineage Specification and Patterning in hESC-derived Gastruloids
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Summary The gastrulation process is controlled by the interplay between morphogenetic signals from BMP, WNT and NODAL pathways. Increasing evidences support an emerging role of the Hippo-YAP signaling in the cell-fate decisions that guide lineage specification in mouse and human Embryonic Stem Cells (hESCs). However, the contribution of YAP to the process of gastrulation in hESCs remains unknown. Here, we show that YAP1 regulates the specification, size and patterning of the three-germ layers. Using hESC-derived 2D-micropatterned gastruloids and directed differentiation approaches we show that YAP maintains a semi-active NODAL signaling during gastrulation essential to regulate the exit of pluripotency. In absence of YAP1, a hyperactive NODAL signaling retains SMAD2.3 in the nuclei, impeding the exit of pluripotency and the acquisition of the ectodermal gene program. Accordingly, the inhibition of NODAL signaling is sufficient to rescue the gastrulation-defective phenotype of the YAP1 KO hESCs. Our work revealed that Hippo-YAP1 signaling is an important component of the developmental network that coordinate hESC pluripotency and gastrulation.
 
Overall design We used a directed differentiation protocol (StemCell Technologies #05230) to induce human embryonic stem cells (hESC) differentiation towards ectoderm, mesoderm and endoderm lineages in WT and YAP1 KO and performed gene expression profiling using RNA-Seq. We also included controls of undifferentiated hESC. In addition, single-nuclei ATAC-seq (snATAC) was used to examine the genome-wide chromatin accessibility profile in WT and YAP1 KO hESCs.
 
Contributor(s) Giraldez S, Stronati E, Hsu H, Huang L, Abraham E, Jones K, Estaras C
Citation(s) 35063126
Submission date Mar 05, 2021
Last update date Mar 28, 2022
Contact name April Elizabeth Williams
E-mail(s) apriljack06@gmail.com, awilliams@salk.edu
Phone 7345461645
Organization name Salk Institute for Biological Studies
Department IGC
Street address 10010 N Torrey Pines Rd
City San Diego
State/province California
ZIP/Postal code 92037
Country USA
 
Platforms (1)
GPL20301 Illumina HiSeq 4000 (Homo sapiens)
Samples (25)
GSM5137551 WT_hESC_snATAC
GSM5137552 YAP_hESC_snATAC
GSM5137553 H1_hESC_H1_Ecto_1
Relations
BioProject PRJNA707055
SRA SRP309504

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
GSE168377_D0_totalPeaks_annotated_pval.txt.gz 18.3 Mb (ftp)(http) TXT
GSE168377_YAP_trilineage_exons_raw.xlsx 3.8 Mb (ftp)(http) XLSX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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