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Temporal Control of Metabolic Amplitude by Nocturnin

The timing of food intake and nutrient utilization is critical to health and regulated partly by the circadian clock. Increased amplitude of circadian oscillations and metabolic output has been found to improve health in diabetic and obesity mouse models. Here, we report a function for the circadian...

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Autores principales: Stubblefield, Jeremy J., Gao, Peng, Kilaru, Gokhul, Mukadam, Bilal, Terrien, Jeremy, Green, Carla B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815321/
https://www.ncbi.nlm.nih.gov/pubmed/29386110
http://dx.doi.org/10.1016/j.celrep.2018.01.011
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author Stubblefield, Jeremy J.
Gao, Peng
Kilaru, Gokhul
Mukadam, Bilal
Terrien, Jeremy
Green, Carla B.
author_facet Stubblefield, Jeremy J.
Gao, Peng
Kilaru, Gokhul
Mukadam, Bilal
Terrien, Jeremy
Green, Carla B.
author_sort Stubblefield, Jeremy J.
collection PubMed
description The timing of food intake and nutrient utilization is critical to health and regulated partly by the circadian clock. Increased amplitude of circadian oscillations and metabolic output has been found to improve health in diabetic and obesity mouse models. Here, we report a function for the circadian deadenylase Nocturnin as a regulator of metabolic amplitude across the day/night cycle and in response to nutrient challenge. We show that mice lacking Nocturnin (Noct(−/−)) display significantly increased amplitudes of mRNA expression of hepatic genes encoding key metabolic enzymes regulating lipid and cholesterol synthesis, both over the daily circadian cycle and in response to fasting and refeeding. Noct(−/−) mice have increased plasma triglyceride throughout the night and increased amplitude of hepatic cholesterol levels. Therefore, posttranscriptional control by Nocturnin regulates the amplitude of these critical metabolic pathways, and loss of this activity results in increased metabolic flux and reduced obesity.
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spelling pubmed-58153212018-02-16 Temporal Control of Metabolic Amplitude by Nocturnin Stubblefield, Jeremy J. Gao, Peng Kilaru, Gokhul Mukadam, Bilal Terrien, Jeremy Green, Carla B. Cell Rep Article The timing of food intake and nutrient utilization is critical to health and regulated partly by the circadian clock. Increased amplitude of circadian oscillations and metabolic output has been found to improve health in diabetic and obesity mouse models. Here, we report a function for the circadian deadenylase Nocturnin as a regulator of metabolic amplitude across the day/night cycle and in response to nutrient challenge. We show that mice lacking Nocturnin (Noct(−/−)) display significantly increased amplitudes of mRNA expression of hepatic genes encoding key metabolic enzymes regulating lipid and cholesterol synthesis, both over the daily circadian cycle and in response to fasting and refeeding. Noct(−/−) mice have increased plasma triglyceride throughout the night and increased amplitude of hepatic cholesterol levels. Therefore, posttranscriptional control by Nocturnin regulates the amplitude of these critical metabolic pathways, and loss of this activity results in increased metabolic flux and reduced obesity. 2018-01-30 /pmc/articles/PMC5815321/ /pubmed/29386110 http://dx.doi.org/10.1016/j.celrep.2018.01.011 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Stubblefield, Jeremy J.
Gao, Peng
Kilaru, Gokhul
Mukadam, Bilal
Terrien, Jeremy
Green, Carla B.
Temporal Control of Metabolic Amplitude by Nocturnin
title Temporal Control of Metabolic Amplitude by Nocturnin
title_full Temporal Control of Metabolic Amplitude by Nocturnin
title_fullStr Temporal Control of Metabolic Amplitude by Nocturnin
title_full_unstemmed Temporal Control of Metabolic Amplitude by Nocturnin
title_short Temporal Control of Metabolic Amplitude by Nocturnin
title_sort temporal control of metabolic amplitude by nocturnin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815321/
https://www.ncbi.nlm.nih.gov/pubmed/29386110
http://dx.doi.org/10.1016/j.celrep.2018.01.011
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