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Status |
Public on Sep 26, 2024 |
Title |
TGF-β and RAS jointly unmask primed enhancers to drive metastasis (RNA-Seq) |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Epithelial-to-mesenchymal transitions (EMTs) and extracellular matrix (ECM) remodeling are distinct yet important processes during carcinoma invasion and metastasis. TGF-β and RAS, signaling through SMAD and RAS-responsive element-binding protein 1 (RREB1), jointly trigger expression of EMT and fibrogenic factors as two discrete arms of a common transcriptional response in carcinoma cells. Here we demonstrate that both arms form a program for lung adenocarcinoma pulmonary metastasis and identify chromatin determinants tying the expression of the constituent genes to TGF-β and RAS dual inputs. RREB1 binds near H4K16ac histone marks and histone H2A.Z-loaded nucleosomes at enhancers in the fibrogenic genes IL11, PDGFB, and HAS2 and the EMT transcription factor SNAI1, priming these enhancers for activation by a SMAD4-INO80 nucleosome remodeling complex in response to TGF-β. These regulatory properties set the fibrogenic EMT program apart from RAS-independent TGF-β gene responses and illuminate the operation and vulnerabilities of a transcriptional program that promotes metastatic outgrowth.
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Overall design |
Expression profiling by high throughput sequencing of 393T3 cells, a cell line derived from a lung tumor from a KrasG12D;p53-/- (KP) genetically engineered mouse model, treated with SB505124 or TGF-β for 1.5 h
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Contributor(s) |
Lee J, Koche RP, Massagué J |
Citation missing |
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Submission date |
Feb 16, 2024 |
Last update date |
Sep 26, 2024 |
Contact name |
Jun Ho Lee |
E-mail(s) |
jhlee90710@gmail.com
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Organization name |
MSKCC
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Street address |
417 E 68th St
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City |
New York |
ZIP/Postal code |
10065 |
Country |
USA |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (12)
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This SubSeries is part of SuperSeries: |
GSE256020 |
TGF-β and RAS jointly unmask primed enhancers to drive metastasis |
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Relations |
BioProject |
PRJNA1077392 |