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Status |
Public on Dec 10, 2016 |
Title |
CTCF modulates Estrogen Receptor function through specific chromatin and nuclear matrix interactions [ChIP-seq] |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
In our work we used high-throughput sequencing methods to get insight in the role of CTCF in ER-mediated gene regulation in luminal breast cancer cells. After assessing genome-wide binding of CTCF, ER, FOXA1 and Lamin B in MCF7 cells treated with estrogen for different time points, we could correlate the interaction to the chromatin with estrogen-induced de novo transcription (from GRO-seq data) and loop formation (from ChIA-PET, Fullwood et al., 2009). We observed that CTCF binding correlates with ER-mediated transcription and its depletion can affect ER-ER loop formation and subsequently gene expression.
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Overall design |
Examination of CTCF, ER, FOXA1 and Lamin B chromatin binding in MCF7 cells upon estrogen stimulation for 0h, 45min or 3h.
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Contributor(s) |
Fiorito E, Sharma Y, Gilfillan S |
Citation(s) |
27638884 |
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Submission date |
Aug 02, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Elisa Fiorito |
E-mail(s) |
elisa.fiorito@ncmm.uio.no
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Organization name |
University of Oslo (UiO)
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Department |
Norwegian Centre for Molecular Medicine (NCMM)
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Lab |
Breast Cancer group
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Street address |
Forskningsparken - Gaustadalleen 21
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City |
Oslo |
ZIP/Postal code |
0349 |
Country |
Norway |
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Platforms (1) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
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Samples (15)
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This SubSeries is part of SuperSeries: |
GSE85108 |
CTCF modulates Estrogen Receptor function through specific chromatin and nuclear matrix interactions |
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Relations |
BioProject |
PRJNA336191 |
SRA |
SRP080814 |