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Status |
Public on Dec 31, 2015 |
Title |
The dynamics of chromatin accessibility during EMT |
Organism |
Homo sapiens |
Experiment type |
Methylation profiling by genome tiling array
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Summary |
The power of our genome-wide survey lies in that we were able to query chromatin accessibility changes concurrently with those in DNA methylation. We identified both opening and closing events, predominantly independent of DNA methylation, in both systems. Our results have powerful implications for future basic and clinical research on this developmental process and its resurfacing during cancer cell metastasis.
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Overall design |
To address epigenetic changes that mediate EMT, we used two models in the human system: EMT induced by the transcriptional repressor Twist as well as EMT induced by TGF-beta. We performed AcceSssIble on these cells at several time points through the course of the transition and identified genes that need to be repressed to allow for the process.
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Contributor(s) |
You JS, Yang X, Pandian K, Liang G, Jones PA |
Citation(s) |
29228692 |
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Submission date |
Nov 17, 2014 |
Last update date |
Mar 22, 2019 |
Contact name |
Xiaojing Yang |
E-mail(s) |
xiaojiny@usc.edu
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Phone |
(323)865-0740
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Organization name |
USC/Norris Comprehensive Cancer Center
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Street address |
1441 Eastlake Ave, Room 7336
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City |
Los Angeles |
State/province |
CA |
ZIP/Postal code |
90033 |
Country |
USA |
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Platforms (1) |
GPL13534 |
Illumina HumanMethylation450 BeadChip (HumanMethylation450_15017482) |
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Samples (16)
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Relations |
BioProject |
PRJNA267574 |