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Status |
Public on Feb 26, 2019 |
Title |
PTENα/β paradoxically promote carcinogenesis through WDR5-H3K4me3 axis [ChIP-seq] |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
we report that USP9X and FBXW11 selectively regulate the stability of PTENα/β but not PTEN proteins by deubiqitination and ubiquitination respectively. USP9X promotes and FBXW11 suppresses tumorigenesis mediated by PTENα/β. In contrast to the current paradigm for PTEN as a tumor suppressor, PTENα/β promote tumorigenesis of cancer cells in a phosphatase-independent manner. Mechanistically, PTENα/β localized in the nucleus regulate expressions of tumor-promoting genes such as NOTCH3 in the similar way as the H3K4 presenter WDR5. Further, PTENα/β but not PTEN directly interact with WDR5 to promote trimethylation of H3K4 and maintain a tumor-promoting signature.
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Overall design |
To confirm the interplay between PTENα/β and WDR5 at gene promoters using by ChIP seq in SMMC-7721
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Contributor(s) |
Shen S, Zhang C, Ge M, Dong S |
Citation missing |
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Submission date |
Feb 24, 2019 |
Last update date |
Feb 27, 2019 |
Contact name |
ge mengkai |
E-mail(s) |
gemengk@sjtu.edu.cn
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Phone |
15201867201
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Organization name |
Shanghai Jiao Tong University School of Medicine (SJTU-SM)
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Street address |
shanghai
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City |
shanghai |
State/province |
State... |
ZIP/Postal code |
13185541251gmk |
Country |
China |
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Platforms (1) |
GPL24676 |
Illumina NovaSeq 6000 (Homo sapiens) |
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Samples (3) |
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This SubSeries is part of SuperSeries: |
GSE126984 |
PTENα/β paradoxically promote carcinogenesis through WDR5-H3K4me3 axis |
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Relations |
BioProject |
PRJNA524003 |
SRA |
SRP186727 |