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Status |
Public on Nov 04, 2019 |
Title |
Ribosome-profiling experiments for “Chronic repression by MAF1 supports futile RNA cycling as a mechanism for obesity resistance” |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing Other
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Summary |
To characterize the translation defects in Maf1-/- samples, we used ribosome profiling on three WT and three Maf1-/- fed livers. Each sample was spiked with a fixed amount of Drosophila S2 Schneider cell material as an internal control for sample-to-sample normalization, and to allow detection of global changes in translation.
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Overall design |
Two conditions (WT of Maf1 KO mice), three biological replicates per condition. For each sample, both Ribosome-protected fragments (RPFL) and total RNA fragments (TOTL) were sequenced.
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Contributor(s) |
Bonhoure N, Praz V, Willis I, Hernandez N |
Citation(s) |
32686713 |
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Submission date |
Oct 02, 2017 |
Last update date |
Jul 25, 2021 |
Contact name |
Nicolo Riggi |
Organization name |
CHUV
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Department |
Département de Pathologie Expérimentale
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Lab |
Institut universitaire de pathologie
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Street address |
Bugnon 25
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City |
Lausanne |
State/province |
VD |
ZIP/Postal code |
1011 |
Country |
Switzerland |
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Platforms (1) |
GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
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Samples (12)
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This SubSeries is part of SuperSeries: |
GSE104535 |
Chronic repression by MAF1 supports futile RNA cycling as a mechanism for obesity resistance |
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Relations |
BioProject |
PRJNA412979 |
SRA |
SRP119310 |