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Series GSE109524 Query DataSets for GSE109524
Status Public on Mar 18, 2019
Title Genome-scale screens identify JNK/JUN signaling as a barrier for pluripotency exit and endoderm differentiation
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Other
Summary Human embryonic and induced pluripotent stem cells (hESCs/hiPSCs) hold great promise for cell-based therapies and drug discovery. However, homogeneous differentiation remains a major challenge, highlighting the need for understanding developmental mechanisms. We performed genome-scale CRISPR screens to uncover regulators of definitive endoderm (DE) differentiation, which unexpectedly uncovered five JNK/JUN family genes as key barriers of DE differentiation. The JNK/JUN pathway does not act through directly inhibiting the DE enhancers. Instead JUN co-occupies ESC enhancers with OCT4, NANOG and SMAD2/3, and specifically inhibits the exit from the pluripotent state by impeding the decommissioning of ESC enhancers and inhibiting the reconfiguration of SMAD2/3 chromatin binding from ESC to DE enhancers. Therefore, the JNK/JUN pathway safeguards pluripotency from precocious DE differentiation. Direct pharmacological inhibition of JNK significantly improves the efficiencies of generating DE and DE-derived pancreatic and lung progenitor cells, highlighting the potential of harnessing the knowledge from developmental studies for regenerative medicine.
 
Overall design We performed genome-wide CRISPR screen using GeCKO and Brunello libraries in hESC to identify regulators of definitive endoderm differentiation. We identified JNK signaling as an inhibitory pathway for definitive endoderm differentiation. We performed RNA-seq, scRNA-seq, ATAC-seq and ChIP-seq to study the role of JNK pathway in DE differentiation.
 
Contributor(s) Li Q
Citation(s) 31110351
Submission date Jan 23, 2018
Last update date Apr 08, 2022
Contact name QINGL LI
Organization name MEMORIAL SLOAN KETTERING CANCER CENTER
Street address 1275 YORK AVE
City NEW YORK
ZIP/Postal code 10065
Country USA
 
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (59)
GSM2945804 Amplicon-Seq_1_GFP-positive
GSM2945805 Amplicon-Seq_2_GFP-positive
GSM2945806 Amplicon-Seq_1_GFP-negative
Relations
BioProject PRJNA431297
SRA SRP131157

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

Supplementary file Size Download File type/resource
GSE109524_RAW.tar 7.2 Gb (http)(custom) TAR (of BW, TXT)
GSE109524_Sup_Data_Set_1_Screen_results_.xlsx 4.2 Mb (ftp)(http) XLSX
GSE109524_Sup_Data_Set_2_RNA-seq_DE_vs_ESC_.xlsx 2.7 Mb (ftp)(http) XLSX
GSE109524_Sup_Data_Set_3_RNA-seq_KO_vs_WT_.xlsx 7.8 Mb (ftp)(http) XLSX
GSE109524_Sup_Data_Set_4_Motif_analysis_.xlsx 29.5 Mb (ftp)(http) XLSX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record
Processed data provided as supplementary file

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