Abstract

The mineralocorticoid receptor (MR) in mammals mediates the effects of aldosterone in regulating fluid balance and potassium homeostasis. While MR signalling is essential for survival in mammals, there is no evidence that MR has any physiological role in ray-finned fish. Teleosts lack aldosterone and emerging evidence suggest that cortisol mediates ion and fluid regulation by activating glucocorticoid receptor (GR) signalling. Consequently, a physiological role for MR signalling, despite its conserved and ancient origin, is still lacking. We tested the hypothesis that a key physiological role for MR signalling in fish is the regulation of stress axis activation and function. Using either MR or GR knockout zebrafish, our results reveal distinct and complementary role for these receptors in stress axis function. GR−/− mutants were hypercortisolemic and failed to elicit a cortisol stress response, while MR−/− mutants showed a delayed, but sustained cortisol response post-stressor. Both these receptors are involved in stress-related behaviour, as the loss of either receptors abolished the glucocorticoid-mediated larval hyperactivity to a light stimulus. Overall, the results underscore a key physiological role for MR signalling in ray-finned fishes, and we propose that the regulation of the highly conserved stress axis as the original function of this receptor.

Highlights

  • The primary role of the mineralocorticoid receptor (MR) in mammals is to mediate the effects of aldosterone in regulating fluid balance and potassium homeostasis

  • While the role of glucocorticoid receptor (GR) is well defined in teleosts, nothing is known about the physiological role directly mediated by MR signalling

  • By comparing corticosteroid receptor (CR) knockout zebrafish lines, we reveal distinct and complementary roles for MR and GR signalling in the development of the stress axis

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Summary

Introduction

The primary role of the mineralocorticoid receptor (MR) in mammals is to mediate the effects of aldosterone in regulating fluid balance and potassium homeostasis. Tissues that lack 11β-HSD2, but still contain MR, suggests that this receptor has an extra-mineralocorticoid role in mammals and activated by glucocorticoids[6,7]. To determine a physiological role for MR signalling in teleosts, and given the ancient origin of this receptor, we tested the hypothesis that MR signalling regulates the highly conserved stress axis function. To this end, we generated ubiquitous MR−/− and GR−/− knockouts in zebrafish (Danio rerio) using CRISPR/Cas[9] mutagenesis. Our results for the first time highlight a key physiological role for MR signalling in fish

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