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mRNA expression explains metabolic and thermal physiology

View ORCID ProfileMelissa Drown, Douglas Crawford, Margie Oleksiak
doi: https://doi.org/10.1101/2022.01.19.477029
Melissa Drown
1University of Miami Rosenstiel School of Marine and Atmospheric Science, 6400 Rickenbacker Causeway, Miami, FL
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  • For correspondence: mxd1288@miami.edu
Douglas Crawford
1University of Miami Rosenstiel School of Marine and Atmospheric Science, 6400 Rickenbacker Causeway, Miami, FL
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Margie Oleksiak
1University of Miami Rosenstiel School of Marine and Atmospheric Science, 6400 Rickenbacker Causeway, Miami, FL
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Abstract

Quantifying mRNA expression, which is heritable and physiologically inducible, reveals biologically important networks and pathways underlying complex traits. Here, we quantify mRNA expression in Fundulus heteroclitus, a small teleost fish, among three populations acclimated to 12°C and 28°C and relate it to variation in six, complex, physiological traits (whole animal metabolism (WAM), critical thermal maximum (CTmax), and four substrate specific cardiac metabolic rates (CaM)). Although 366 heart mRNAs and 528 brain mRNAs had significant differential expression between the two acclimation temperatures, none of the mRNA acclimation responses were shared across all three populations in any tissue. Yet, within an acclimation temperature across all three populations, weighted gene co-expression network analyses show that mRNA expression patterns explained WAM, CTmax, and CaM trait variation. These analyses revealed 9 significant heart MEs (first principal component of module expression) and 4 significant brain MEs. Heart MEs explained variation in WAM, CTmax, and two of the four substrate specific cardiac metabolic rates at 12°C, and CTmax at 28C. In contrast, brain MEs explained CTmax and WAM at 28°C but not at 12°C. Combining MEs as multiple correlations, 82% of variation in WAM at 12°C was explained by four heart MEs, 80% of variation in fatty-acid CaM at 12°C was explained by three heart MEs, and 72% of variation in CTmax at 28°C was explained by three brain MEs. These MEs were enriched for Kyoto Encyclopedia of Genes and Genomes (KEGG) terms related to specific metabolic pathways, suggesting that they represent biologically relevant pathways. Together these data suggest that mRNA co-expression explains complex traits; moreover, physiological traits are more reliant on heart expression at 12°C and brain expression at 28°C.

Author Summary Despite an abundance of genomic data, the molecular and genetic underpinnings of complex traits remain poorly understood. To better understand the molecular basis of complex traits, we used heart and brain mRNA expression to explain complex traits- physiological responses to temperature- in individuals collected from three saltmarsh fish (Fundulus heteroclitus) populations acclimated to 12°C and 28°C. We found that while physiological traits did not differ among populations, the mRNAs important for acclimation responses were >88% unique to a single population and differed between heart and brain tissues. We also found tissue specific co-expressed mRNAs that explain up to 82% of complex traits including whole animal metabolism, upper thermal tolerance, and substrate specific cardiac metabolism measured at 12°C or 28°C acclimation conditions. Notably, sets of co-expressed mRNAs related to these traits are enriched for molecular pathways affecting metabolism, giving insight into the molecular underpinnings of these traits.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted January 22, 2022.
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mRNA expression explains metabolic and thermal physiology
Melissa Drown, Douglas Crawford, Margie Oleksiak
bioRxiv 2022.01.19.477029; doi: https://doi.org/10.1101/2022.01.19.477029
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mRNA expression explains metabolic and thermal physiology
Melissa Drown, Douglas Crawford, Margie Oleksiak
bioRxiv 2022.01.19.477029; doi: https://doi.org/10.1101/2022.01.19.477029

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