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Status |
Public on Oct 04, 2018 |
Title |
TET2 coactivates gene expression through demethylation of enhancers |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing Expression profiling by high throughput sequencing Methylation profiling by high throughput sequencing
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Summary |
The tet methylcytosine dioxygenase 2 (TET2) enzyme catalyzes the conversion of the modified DNA base 5-methylcytosine to 5-hydroxymethylcytosine. TET2 is frequently mutated or dysregulated in multiple human cancers, and loss of TET2 is associated with changes in DNA methylation patterns. Here, using newly developed TET2-specific antibodies and the estrogen response as a model system for studying the regulation of gene expression, we demonstrate that endogenous TET2 occupies active enhancers and facilitates the proper recruitment of ERalpha. Knockout of TET2 by CRISPR-CAS9 leads to a global increase of DNA-methylation at enhancers resulting in attenuation of the estrogen response. We further identified a positive feedback loop between TET2 and ERalpha, which further requires MLL3/COMPASS at these enhancers. Together, this study reveals an epigenetic axis coordinating a transcriptional program through enhancer activation via DNA demethylation.
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Overall design |
To examine changes in histone modifications, ER-alpha occupancy, MLL3 occupancy, and gene expression changes after depletion of TET2 in human breast cancer cell lines.
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Contributor(s) |
Wang L, Ozark PA, Shilatifard A |
Citation(s) |
30417100 |
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Submission date |
Oct 02, 2018 |
Last update date |
Mar 26, 2019 |
Contact name |
Ali Shilatifard |
E-mail(s) |
[email protected]
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Organization name |
Northwestern University Feinberg School of Medicine
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Department |
Department of Biochemistry and Molecular Genetics
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Lab |
Shilatifard Lab
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Street address |
320 E Superior St
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City |
Chicago |
State/province |
IL |
ZIP/Postal code |
60611 |
Country |
USA |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (79)
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Relations |
BioProject |
PRJNA494397 |
SRA |
SRP163132 |