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Status |
Public on Jul 25, 2022 |
Title |
TRIM37 augments AP-2γ transcriptional activity and cellular localization via K63-linked polyubiquitination to drive breast cancer progression [RNA-seq] |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Using a proteomics approach, we identified the Tripartite Motif Containing 37 (TRIM37) as a novel transcriptional coactivator of AP-2γ. We demonstrate TRIM37 facilitates AP-2γ chromatin binding to regulate the AP-2γ mediated transcriptional program directly. We provide evidence that TRIM37 achieves this by stimulating K63-chain-linked polyubiquitination of AP-2γ, promoting protein localization from the cytoplasm to the nucleus. In clinical analyses, we find TRIM37 is upregulated in multiple breast cancer datasets, supporting our findings that TRIM37-AP-2γ interaction is essential for breast cancer tumor growth. Overall, our work revealed that TRIM37 is an oncogenic coactivator of AP-2γ in breast cancer and provides a novel therapeutic target for treating the disease.
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Overall design |
RNA-seq following TRIM37 or AP-2γ knockdown in MCF-7 cells
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Contributor(s) |
Cheung E, Cui G, Narwade N |
Citation(s) |
35864973 |
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Submission date |
Aug 22, 2021 |
Last update date |
Jul 25, 2022 |
Contact name |
Edwin Chong Wing CHEUNG |
E-mail(s) |
ECheung@um.edu.mo
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Organization name |
University of Macau
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Department |
Faculty of Health Sciences
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Lab |
Edwin CHEUNG's lab
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Street address |
Avenida da Universidade, Taipa
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City |
Macau |
State/province |
Macau |
ZIP/Postal code |
999078 |
Country |
China |
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Platforms (1) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
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Samples (3) |
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This SubSeries is part of SuperSeries: |
GSE182547 |
TRIM37 augments AP-2γ transcriptional activity and cellular localization via K63-linked polyubiquitination to drive breast cancer progression. |
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Relations |
BioProject |
PRJNA756730 |
SRA |
SRP333584 |