NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE136870 Query DataSets for GSE136870
Status Public on Jan 24, 2020
Title Mouse ESCs (ES-D3) with Ash2l depletion
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary We showed a novel mechanism in which Ash2l directly binds to super-enhancers of several stemness genes to regulate pluripotency and self-renewal in pluripotent stem cells. Ash2l recruits Oct4/Sox2/Nanog (OSN) to form Ash2l/OSN complex at the super-enhancers of Jarid2, Nanog, Sox2, and Oct4, and further drives enhancer activation, upregulation of stemness genes, and maintains the pluripotent circuitry. Ash2l knockdown abrogates the OSN recruitment to all super-enhancers and further hinders the enhancer activation.
 
Overall design Mouse ESCs (ES-D3) were infected with lentivirus containing either control or shRNA targeting Ash2l sequence. DNA was then extracted from both samples and subjected to ChIP-seq analysis.
 
Contributor(s) Tsai P, Chiou S
Citation(s) 31555818
Submission date Sep 04, 2019
Last update date Jan 24, 2020
Contact name Pinghsing Tsai
Organization name Taipei Veterans General Hospital
Street address Rm. 719, 7F., No.322, Sec. 2, Shipai Rd., Beitou D
City Taipei
State/province Taiwan
ZIP/Postal code 11267
Country Taiwan
 
Platforms (1)
GPL21273 HiSeq X Ten (Mus musculus)
Samples (13)
GSM4060028 shCtrl-Oct4_ChIPSeq
GSM4060029 shAsh2l-Oct4_ChIPSeq
GSM4060030 shCtrl-Sox2_ChIPSeq
Relations
BioProject PRJNA563897
SRA SRP220339

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
GSE136870_Antibody-information.xlsx 9.2 Kb (ftp)(http) XLSX
GSE136870_RAW.tar 1.4 Mb (http)(custom) TAR (of BIGWIG)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap