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Multiomics reveals multilevel control of renal and systemic metabolism by the renal tubular circadian clock
Yohan Bignon, Leonore Wigger, Camille Ansermet, Benjamin D. Weger, Sylviane Lagarrigue, Gabriel Centeno, Fanny Durussel, Lou Götz, Mark Ibberson, Sylvain Pradervand, Manfredo Quadroni, Meltem Weger, Francesca Amati, Frédéric Gachon, Dmitri Firsov
Yohan Bignon, Leonore Wigger, Camille Ansermet, Benjamin D. Weger, Sylviane Lagarrigue, Gabriel Centeno, Fanny Durussel, Lou Götz, Mark Ibberson, Sylvain Pradervand, Manfredo Quadroni, Meltem Weger, Francesca Amati, Frédéric Gachon, Dmitri Firsov
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Research Article Nephrology

Multiomics reveals multilevel control of renal and systemic metabolism by the renal tubular circadian clock

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Abstract

Circadian rhythmicity in renal function suggests rhythmic adaptations in renal metabolism. To decipher the role of the circadian clock in renal metabolism, we studied diurnal changes in renal metabolic pathways using integrated transcriptomic, proteomic, and metabolomic analysis performed on control mice and mice with an inducible deletion of the circadian clock regulator Bmal1 in the renal tubule (cKOt). With this unique resource, we demonstrated that approximately 30% of RNAs, approximately 20% of proteins, and approximately 20% of metabolites are rhythmic in the kidneys of control mice. Several key metabolic pathways, including NAD+ biosynthesis, fatty acid transport, carnitine shuttle, and β-oxidation, displayed impairments in kidneys of cKOt mice, resulting in perturbed mitochondrial activity. Carnitine reabsorption from primary urine was one of the most affected processes with an approximately 50% reduction in plasma carnitine levels and a parallel systemic decrease in tissue carnitine content. This suggests that the circadian clock in the renal tubule controls both kidney and systemic physiology.

Authors

Yohan Bignon, Leonore Wigger, Camille Ansermet, Benjamin D. Weger, Sylviane Lagarrigue, Gabriel Centeno, Fanny Durussel, Lou Götz, Mark Ibberson, Sylvain Pradervand, Manfredo Quadroni, Meltem Weger, Francesca Amati, Frédéric Gachon, Dmitri Firsov

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Figure 5

Alterations of renal fatty acid metabolism in cKOt mice.

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Alterations of renal fatty acid metabolism in cKOt mice.
Schematic (cent...
Schematic (center) and temporal plots (edges) of FA metabolism depicting major renal metabolites (peach), transcripts (yellow), and proteins (green) involved in FA entry and activation, acyl-carnitine shuttle into mitochondria, and acyl-CoA β-oxidation. Proteins surrounded with red are rate limiting. Numbers link components of the schematic to temporal plots. Rhythmicity model and Padj obtained, respectively, from the DryR comparison of rhythmicity pattern and limma R package mean expressions comparison in Ctrl and cKOt mice are mentioned in each plot. ACADL, acyl-coenzyme A dehydrogenase, long chain; ACSL4, acyl-CoA synthetase long chain family member 4; CACT, mitochondrial carnitine/acylcarnitine carrier protein; CD36, cluster of differentiation 36 also known as fatty acid translocase (FAT); CPT1A, Carnitine palmitoyltransferase 1A; CPT2, carnitine palmitoyltransferase 2; CRAT, carnitine O-acetyltransferase; FATP2, fatty acid transport protein 2.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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