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Status |
Public on Sep 01, 2021 |
Title |
FNDC-1-Mediated Mitophagy and ATFS-1 Coordinate to Protect Against Hypoxia-Reoxygenation |
Organism |
Caenorhabditis elegans |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Mitochondrial Quality Control (MQC) balances organelle adaptation and elimination, and mechanistic crosstalk between the underlying molecular processes impacts subsequent stress outcomes. FUN14 Domain Containing 1 (FUNDC1) is a mammalian mitophagy receptor that responds to hypoxia-reoxygenation (HR) stress. Here, we provide evidence that FNDC-1 is the C. elegans ortholog of FUNDC1, and that its loss protects against injury in a worm model of HR. This protection depends upon ATFS-1, a transcription factor that is central to the mitochondrial unfolded protein response (UPRmt). Global mRNA and metabolite profiling suggest that atfs-1 dependent stress responses and metabolic remodeling occur in response to the loss of fndc-1. These data support a role for FNDC-1 in non-hypoxic MQC, and further suggest that these changes are prophylactic in relation to subsequent HR. Our results highlight functional coordination between mitochondrial adaptation and elimination that organizes stress responses and metabolic rewiring to protect against HR injury.
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Overall design |
3 strains were profiled, wild type (N2), fndc-1(rny14) and atfs-1(tm4525);fndc-1(rny14), with 5 biological samples of each strain, for a total of 15 samples. Synchronized populations were grown to day 1 of adulthood, then harvested for RNA.
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Contributor(s) |
Nehrke K, Lim Y |
Citation(s) |
33416042 |
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Submission date |
Sep 27, 2020 |
Last update date |
Dec 01, 2021 |
Contact name |
keith nehrke |
E-mail(s) |
[email protected]
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Phone |
5852757020
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Organization name |
University of Rochester Medical Center
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Department |
Medicine
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Street address |
1514 Rush Scottsville Rd
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City |
Rush |
State/province |
NY |
ZIP/Postal code |
14543 |
Country |
USA |
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Platforms (1) |
GPL19757 |
Illumina NextSeq 500 (Caenorhabditis elegans) |
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Samples (15)
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Relations |
BioProject |
PRJNA666012 |
SRA |
SRP285549 |