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Status |
Public on May 08, 2019 |
Title |
Measuring the influence of RNA binding proteins on A-to-I RNA editing in the Drosophila brain |
Organism |
Drosophila melanogaster |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
A-to-I RNA editing levels differ across tissues and cell types, but regulators of the editing process are largely unknown. We used RNA-seq on whole fly brains with different RNA binding proteins knocked down to test for A-to-I RNA editing level differences between controls and knockdowns.
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Overall design |
To screen for editing regulators in the Drosophila brain, we crossed a pan-neuronal Gal4 driver, C155-Gal4, to different UAS-shRNA lines targeting individual RNA binding proteins, extracted RNA and made RNA-seq libraries. We sequenced four total replicates of shGFP controls and two replicates of all RNA binding protein knockdowns.
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Contributor(s) |
Sapiro AL, Qiao H, Ni J, Li JB |
Citation(s) |
32433963 |
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Submission date |
Feb 15, 2019 |
Last update date |
Jun 29, 2020 |
Contact name |
Jin Billy Li |
E-mail(s) |
[email protected]
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Organization name |
Stanford University
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Department |
Genetics
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Street address |
300 Pasteur Dr, Alway M341
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City |
Stanford |
State/province |
CA |
ZIP/Postal code |
94305 |
Country |
USA |
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Platforms (1) |
GPL19132 |
Illumina NextSeq 500 (Drosophila melanogaster) |
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Samples (48)
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This SubSeries is part of SuperSeries: |
GSE126631 |
Zinc finger RNA binding protein Zn72D regulates ADAR-mediated RNA editing in neurons |
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Relations |
BioProject |
PRJNA522773 |
SRA |
SRP186005 |