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Series GSE183046 Query DataSets for GSE183046
Status Public on Dec 31, 2021
Title ChIP-seq on Zfp961 GFP flox/flox mESCs to verify Zfp961 repression capacity to transcription of ERVKs
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary We performed ChIP-seq assay with anti-KAP1 antibodies on Zfp961-GFPflox/flox ESCs.We found KAP1 signal decreased at PBS-Lys sites in Zfp961 KO cells compared to WT, suggesting Zfp961 recruiting KAP1 to ERV-K regions. We performed H3K27ac ChIP on Zfp961 WT or KO mESCs. We found that H3k27ac modification at PBS-Lys sites was elevated upon Zfp961 deletion, indicating Zfp961 serving as a repressive transcription factor.
 
Overall design Basically, Zfp961-GFP floxed mESCs cell lines treated with 4-OHT or etOH as control were used for anti-KAP1 ChIP and anti-H3K27ac ChIP.
 
Contributor(s) Yang B
Citation(s) 35259018
Submission date Aug 30, 2021
Last update date Mar 31, 2022
Contact name Bo Yang
E-mail(s) yangbo2099@sina.cn
Phone 15221512158
Organization name The Third Affiliated Hospital of Guangzhou Medical University
Lab Lab of Sun
Street address Guangzhou, 510150, Guangdong Province, China.
City Guangzhou
State/province Guangdong
ZIP/Postal code 510150
Country China
 
Platforms (1)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (4)
GSM5550097 WT KAP1 ChIP
GSM5550098 KO KAP1 ChIP
GSM5550099 WT H3K27ac ChIP
Relations
BioProject PRJNA758952
SRA SRP334738

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

Supplementary file Size Download File type/resource
GSE183046_RAW.tar 1.0 Gb (http)(custom) TAR (of BIGWIG)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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