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Status |
Public on Feb 20, 2017 |
Title |
RNA sequencing data from beta-catenin activated, E2-2 wildtype and beta-catenin activated, E2-2 deleted cultured fetal mouse kidneys. |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Oncogenic stabilizing mutations in the beta-catenin gene CTNNB1 are common in one class of human Wilms tumors. To model these tumors, we crossed mice carrying an inducible Cre recombinase (Rosa26-CreERT2) with a conditional gain-of-function beta-catenin allele (Ctnnb1Ex3flox). We obtained kidneys at embryonic day 13.5 and placed them in organ culture with tamoxifen. Multiple small tumors formed in the Ctnnb1∆Ex3 kidneys while the control kidneys developed normally. Immunostaining for Sall1, a marker of condensing metanephric mesenchyme, indicated that the tumors arise from this tissue compartment, analogous to the origin of human Wilms tumors. Expression profiling identified a set of induced genes overlapping with those up-regulated in human Wilms tumors with CTNNB1 mutations, including genes encoding feedback inhibitors of Wnt/beta-catenin signaling, the epithelial-mesenchymal transition (EMT) inducers, and the transcription factor E2-2 (ITF2/TCF4). A conditional deletion of E2-2 showed that this gene is important for growth of the nephroblastomas, in part via promoting an epithelial to mesenchymal transition downstream of beta-catenin. Given these cross-species validations, and genetic proof of the oncogenic function of a key downstream target gene, we expect that this rapid and efficient organ culture model will be useful for further studies to dissect and inhibit oncogenic Wnt/beta-catenin signaling.
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Overall design |
The expression of 4 beta-catenin activated, E2-2 wildtype cultured fetal mouse kidneys was compared with 3 beta-catenin activated, E2-2 deleted cultured fetal mouse kidneys.
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Contributor(s) |
Yotova I, Tycko B |
Citation missing |
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Submission date |
Nov 18, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Emily Hsu |
Organization name |
Columbia University
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Department |
ICG
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Lab |
Tycko Lab
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Street address |
1130 St. Nicholas Ave.
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City |
New York |
State/province |
NY |
ZIP/Postal code |
10032 |
Country |
USA |
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Platforms (1) |
GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
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Samples (7)
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This SubSeries is part of SuperSeries: |
GSE65899 |
Dissection of functionally relevant Wnt/beta-catenin target genes in an organ culture model of Wilms tumor |
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Relations |
BioProject |
PRJNA268204 |
SRA |
SRP050140 |