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Multiomics reveals multilevel control of renal and systemic metabolism by the renal tubular circadian clock
Yohan Bignon, … , Frédéric Gachon, Dmitri Firsov
Yohan Bignon, … , Frédéric Gachon, Dmitri Firsov
Published March 2, 2023
Citation Information: J Clin Invest. 2023;133(8):e167133. https://doi.org/10.1172/JCI167133.
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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 3

Alterations of renal and plasma metabolomes in cKOt mice.

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Alterations of renal and plasma metabolomes in cKOt mice.
(A) Donut char...
(A) Donut charts showing the percentage of rhythmic, nonrhythmic, and unassigned renal metabolites in control (Ctrl) and cKOt mice. (B) Venn diagram showing the number of rhythmic metabolites in kidneys of Ctrl and cKOt mice. (C) Histogram showing the acrophase distribution of rhythmic metabolites in kidneys of Ctrl and cKOt mice. Red dashed lines: kernel density estimates. (D) Cumulative number of rhythmic metabolites in Ctrl and cKOt mice in function of amplitude. (E) Donut charts showing the proportion of renal metabolites showing an increased, decreased, or not significantly altered mean level according to limma R package in cKOt versus Ctrl mice for each class of metabolites. (F) Volcano plot depicting metabolites significantly (Padj < 0.05) more abundant (purple dots) or less abundant (yellow dots) in kidneys of cKOt mice compared with Ctrl mice. (G) Donut charts showing the percentage of rhythmic, nonrhythmic, and unassigned plasma metabolites in Ctrl and cKOt mice. (H) Venn diagram showing the number of rhythmic metabolites in plasma of Ctrl and cKOt mice. (I) Histogram showing the acrophase distribution of rhythmic metabolites in plasma samples of Ctrl and cKOt mice. Red dashed lines: kernel density estimates. (J) Volcano plot depicting metabolites significantly (Padj < 0.05) more abundant (purple dots) or less abundant (yellow dots) in the plasma of cKOt mice compared with Ctrl mice. (K) Donut charts showing the proportion of plasma metabolites showing an increased, decreased, or not significantly altered mean level according to limma R package in cKOt versus Ctrl mice for each class of metabolite. (L) Temporal plots showing the plasma concentration, dryR rhythmicity model, and limma R package result of mean expression comparison between Ctrl and cKOt mice for carnitine, acetylcarnitine, propionylcarnitine, and creatinine in plasma metabolomes of Ctrl and cKOt mice.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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