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Series GSE66601 Query DataSets for GSE66601
Status Public on Dec 01, 2015
Title Genome-wide characterization of ARID3B binding sites and KDM4C in ARID3B-knockout OECM1 cells
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary In this study we assayed for genome-wide localization of ARID3B and KDM4C enrichment in control and ARID3B-knockout OECM1 cells. The expression of the embryonic stem cell (ESC) signature in cancer cells indicates the coordinated regulation of the stemness genes in cancer stem cells, which are responsible for cancer initiation and dissemination. let-7 family microRNAs are crucial regulators for stem cell differentiation. In cancer cells, let-7 suppresses cancer stemness through targeting different oncogenes such as c-Myc, RAS, and HMGA2. However, most let-7 target genes are oncogenes rather than stemness factors, and the mechanism of let-7-repressed stemness is unclear. Here we demonstrate that let-7 supresses the formation of AT-rich interacting domain 3B (ARID3B) complex through targeting the expression of ARID3B, the interacting partner ARID3A, and importin 9. ARID3B complex recruits histone demethylase 4C (KDM4C) to the regulatory region of stemness genes for reducing histone 3 lysine 9 trimethylation, resulting in an open configuration of the chromatin of stemness genes. In cancer tissues, ARID3B expression correlates with the nuclear ARID3A expression and a worse prognosis. This result highlights the role of let-7 in regulating stemness through histone modifications.
 
Overall design The Cas9/gRNA target sites containing20 bp gRNA sequence plus the PAM sequence (NGG) using Jack Lin’s CRISPR/Cas9 gRNA finder tool. The gRNA using for knockout ARID3B was predicted by blasting with human genomic and transcript sequences using the NCBI/blastn suite for the detection of potential off-targets.
 
Contributor(s) Muh-Hwa Y, Tsai-Tsen L
Citation(s) 26776511
Submission date Mar 06, 2015
Last update date May 15, 2019
Contact name Tsai-Tsen Liao
Phone +886-228235870
Organization name Institute of Clinical Medicine
Lab Dr. M.H. Yang's Lab
Street address No.201, Sec.2, Shih-Pai Rd. Peitou, Taipei, Taiwan, 11221, R.O.C
City Taipei
State/province State...
ZIP/Postal code 11221
Country Taiwan
 
Platforms (1)
GPL9052 Illumina Genome Analyzer (Homo sapiens)
Samples (4)
GSM1626088 Control_ARID3B
GSM1626089 ARID3B-KD_ARID3B
GSM1626090 Control_KDM4C
This SubSeries is part of SuperSeries:
GSE66603 let-7 controls cancer stemness through ARID3B
Relations
BioProject PRJNA277434
SRA SRP055904

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
GSE66601_RAW.tar 220.0 Kb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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