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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
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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.
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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.
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Contributor(s) |
Yang B |
Citation(s) |
35259018 |
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Submission date |
Aug 30, 2021 |
Last update date |
Mar 31, 2022 |
Contact name |
Bo Yang |
E-mail(s) |
yangbo2099@sina.cn
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Phone |
15221512158
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Organization name |
The Third Affiliated Hospital of Guangzhou Medical University
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Lab |
Lab of Sun
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Street address |
Guangzhou, 510150, Guangdong Province, China.
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City |
Guangzhou |
State/province |
Guangdong |
ZIP/Postal code |
510150 |
Country |
China |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (4)
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Relations |
BioProject |
PRJNA758952 |
SRA |
SRP334738 |