A1 Refereed original research article in a scientific journal
Tissue-specific metabolic enzyme levels covary with whole-animal metabolic rates and life-history loci via epistatic effects
Authors: Prokkola Jenni M., Chew Kuan Kiat, Anttila Katja, Maamela Katja S., Yildiz Atakan, Åsheim Eirik R., Primmer Craig R., Aykanat Tutku
Publisher: Royal Society
Publication year: 2024
Journal: Philosophical Transactions B: Biological Sciences
Journal name in source: Philosophical Transactions of the Royal Society B: Biological Sciences
Article number: 20220482
Volume: 379
Issue: 1896
eISSN: 1471-2970
DOI: https://doi.org/10.1098/rstb.2022.0482(external)
Web address : https://royalsocietypublishing.org/doi/abs/10.1098/rstb.2022.0482(external)
Self-archived copy’s web address: https://research.utu.fi/converis/portal/detail/Publication/386809480(external)
Metabolic rates, including standard (SMR) and maximum (MMR) metabolic rate have often been linked with life-history strategies. Variation in context- and tissue-level metabolism underlying SMR and MMR may thus provide a physiological basis for life-history variation. This raises a hypothesis that tissue-specific metabolism covaries with whole-animal metabolic rates and is genetically linked to life history. In Atlantic salmon (Salmo salar), variation in two loci, vgll3 and six6, affects life history via age-at-maturity as well as MMR. Here, using individuals with known SMR and MMR with different vgll3 and six6 genotype combinations, we measured proxies of mitochondrial density and anaerobic metabolism, i.e. maximal activities of the mitochondrial citrate synthase (CS) and lactate dehydrogenase (LDH) enzymes, in four tissues (heart, intestine, liver, white muscle) across low- and high-food regimes. We found enzymatic activities were related to metabolic rates, mainly SMR, in the intestine and heart. Individual loci were not associated with the enzymatic activities, but we found epistatic effects and genotype-by-environment interactions in CS activity in the heart and epistasis in LDH activity in the intestine. These effects suggest that mitochondrial density and anaerobic capacity in the heart and intestine may partly mediate variation in metabolic rates and life history via age-at-maturity.
This article is part of the theme issue ‘The evolutionary significance of variation in metabolic rates’.
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