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Status |
Public on Sep 20, 2013 |
Title |
Genome-wide analysis of dFOXO binding sites in Drosophila |
Organism |
Drosophila melanogaster |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
To understand how reduced insulin/IGF-1 signaling extends Drosophila lifespan through its downstream transcription factor dFOXO. We conducted ChIP analysis with a dFOXO antibody followed by Illumina high-throughput sequencing from chico heterozygous mutants, which are long-lived and normal sized, and from adult flies with ablated insulin producing cells (IPCs), which are also long-lived. dFOXO bound at promoters of 273 genes common among these genotypes, thus potentially enriching for shared factors in control of aging.
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Overall design |
Two replicates were sequenced from chico heterozygous mutants and IPC ablated flies.
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Contributor(s) |
Bai H, Tatar M |
Citation(s) |
24244197 |
Submission date |
Feb 26, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Hua Bai |
E-mail(s) |
hua_bai@brown.edu
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Organization name |
Brown University
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Department |
EEB
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Lab |
Marc Tatar Lab
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Street address |
34 Olive St, BMC502
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City |
Providence |
State/province |
RI |
ZIP/Postal code |
02912 |
Country |
USA |
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Platforms (1) |
GPL11203 |
Illumina Genome Analyzer IIx (Drosophila melanogaster) |
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Samples (8)
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Relations |
BioProject |
PRJNA191574 |
SRA |
SRP018869 |