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Status |
Public on Aug 01, 2014 |
Title |
E2a is necessary for Smad2/3 dependent transcription and the direct repression of lefty |
Organism |
Xenopus tropicalis |
Experiment type |
Expression profiling by high throughput sequencing Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We characterized the binding of Smad2/3 using ChIP-SEQ in both control gastrula-stage X. tropicalis embryos and embryos depleted of the transcription factor E2a (E2a-MO). We also characterized gene expression in control and E2a-depleted embryos by RNA-Seq. For ChIP-Seq, three biological replicates of E2a-MO were performed, and two biological replicates of Control embryos were performed. For RNA-Seq, two biological replicates of E2a-MO were performed, and two biological replicates of Control embryos were performed, and the mean expression levels of each gene were compared.
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Overall design |
For ChIP-Seq, three biological replicates were performed for E2a-depleted X. tropicalis embryos, and two biological replicates were performed for control gastrula-stage embryos. For RNA-Seq, two biological replicates were performed for both E2a-depleted embryos and control embryos, and the mean expression levels were compared for each gene.
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Contributor(s) |
Wills AE, Baker JC |
Citation(s) |
25669884 |
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Submission date |
Mar 25, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Andrea E. Wills |
Organization name |
Stanford School of Medicine
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Department |
Genetics
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Lab |
Julie Baker
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Street address |
300 Pasteur Drive
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City |
Stanford |
State/province |
CA |
ZIP/Postal code |
94305 |
Country |
USA |
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Platforms (2) |
GPL9320 |
Illumina Genome Analyzer II (Xenopus (Silurana) tropicalis) |
GPL15472 |
Illumina HiSeq 2000 (Xenopus (Silurana) tropicalis) |
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Samples (11)
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Relations |
BioProject |
PRJNA242626 |
SRA |
SRP040548 |