Epigenetic and post-transcriptional repression support metabolic suppression in chronically hypoxic goldfish

• Published in: Scientific reports Vol. 12; no. 1; pp. 5576 - 16
• Main Authors: Farhat, Elie, Talarico, Giancarlo G. M., Grégoire, Mélissa, Weber, Jean-Michel, Mennigen, Jan A.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 02.04.2022; Nature Publishing Group; Nature Portfolio
• Subjects: 631/337/176; 631/337/384; 631/337/572; 631/443/319; Animals; Biosynthesis; Carassius auratus; Cholesterol; DNA methylation; Energy expenditure; Epigenesis, Genetic; Epigenetics; Epigenomics; Gene Expression; Gene silencing; Goldfish - genetics; Humanities and Social Sciences; Hypoxia; Hypoxia - genetics; Hypoxia - metabolism; Lipid composition; Lipid metabolism; Metabolism; miRNA; Mitochondria; multidisciplinary; Oxidation; Oxygen; Post-transcription; Rapamycin; Science; Science (multidisciplinary); Tissues; TOR protein
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-022-09374-8

Goldfish enter a hypometabolic state to survive chronic hypoxia. We recently described tissue-specific contributions of membrane lipid composition remodeling and mitochondrial function to metabolic suppression across different goldfish tissues. However, the molecular and especially epigenetic foundations of hypoxia tolerance in goldfish under metabolic suppression are not well understood. Here we show that components of the molecular oxygen-sensing machinery are robustly activated across tissues irrespective of hypoxia duration. Induction of gene expression of enzymes involved in DNA methylation turnover and microRNA biogenesis suggest a role for epigenetic transcriptional and post-transcriptional suppression of gene expression in the hypoxia-acclimated brain. Conversely, mechanistic target of rapamycin-dependent translational machinery activity is not reduced in liver and white muscle, suggesting this pathway does not contribute to lowering cellular energy expenditure. Finally, molecular evidence supports previously reported chronic hypoxia-dependent changes in membrane cholesterol, lipid metabolism and mitochondrial function via changes in transcripts involved in cholesterol biosynthesis, β-oxidation, and mitochondrial fusion in multiple tissues. Overall, this study shows that chronic hypoxia robustly induces expression of oxygen-sensing machinery across tissues, induces repressive transcriptional and post-transcriptional epigenetic marks especially in the chronic hypoxia-acclimated brain and supports a role for membrane remodeling and mitochondrial function and dynamics in promoting metabolic suppression.