|
Status |
Public on Oct 15, 2019 |
Title |
Transcriptional redirection of activated SKN-1/NRF2 abates the negative metabolic outcomes of a perceived pathogen infection |
Organism |
Caenorhabditis elegans |
Experiment type |
Expression profiling by high throughput sequencing
|
Summary |
Optimal health requires perpetual transcriptional fidelity of gene expression. SKN-1/NRF2 is a cytoprotective transcription factor in C. elegans that regulates the expression of cellular defenses during stress, including: nutrient deprivation, redox imbalance, and xenobiotic and pathogen exposure. Constitutive activation of SKN-1 results in pleiotropic outcomes, including shortened lifespan and protective redistribution of somatic fat to the germline. We measured lipid distribution between the soma and germ tissues after manipulation of SKN-1 activity. Modulating the epigenetic landscape refines SKN-1 activity away from innate immunity targets and alleviates negative metabolic outcomes. Similarly, paraquat exposure redirects SKN-1 activity toward oxidative stress responses and away from pathogen response genes, which restores lipid distribution across tissues. Lastly, activating p38 MAPK signaling is sufficient to drive SKN-1-dependent loss of somatic fat. These data reveal a coordination of organismal metabolic homeostasis with pathogen responses and identifies mechanisms for counteracting the pleiotropic consequences of aberrant transcriptional activity.
|
|
|
Overall design |
Our study aim to look at transcriptional signatures that changes in Day 3 adults, when loss of fat phenotype occurs in constitutively active SKN-1 worms compared to wild type. We are also interested in transcriptional changes when that loss of fat phenotype is suppressed by paraquat exposure or chromatin restriction.
|
|
|
Contributor(s) |
Nhan J, Curran S |
Citation(s) |
31611372 |
|
Submission date |
Dec 10, 2018 |
Last update date |
Nov 12, 2019 |
Contact name |
Sean Curran |
E-mail(s) |
[email protected]
|
Organization name |
University of Southern California
|
Department |
Davis School of Gerontology
|
Lab |
Curran
|
Street address |
3715 McClintock Ave
|
City |
Los Angeles |
State/province |
CA |
ZIP/Postal code |
90089 |
Country |
USA |
|
|
Platforms (1) |
GPL13657 |
Illumina HiSeq 2000 (Caenorhabditis elegans) |
|
Samples (15)
|
|
Relations |
BioProject |
PRJNA509132 |
SRA |
SRP173212 |