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KLF10 integrates circadian timing and sugar signaling to coordinate hepatic metabolism
The mammalian circadian timing system and metabolism are highly interconnected, and disruption of this coupling is associated with negative health outcomes. Krüppel-like factors (KLFs) are transcription factors that govern metabolic homeostasis in various organs. Many KLFs show a circadian expressio...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410083/ https://www.ncbi.nlm.nih.gov/pubmed/34402428 http://dx.doi.org/10.7554/eLife.65574 |
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author | Ruberto, Anthony A Gréchez-Cassiau, Aline Guérin, Sophie Martin, Luc Revel, Johana S Mehiri, Mohamed Subramaniam, Malayannan Delaunay, Franck Teboul, Michèle |
author_facet | Ruberto, Anthony A Gréchez-Cassiau, Aline Guérin, Sophie Martin, Luc Revel, Johana S Mehiri, Mohamed Subramaniam, Malayannan Delaunay, Franck Teboul, Michèle |
author_sort | Ruberto, Anthony A |
collection | PubMed |
description | The mammalian circadian timing system and metabolism are highly interconnected, and disruption of this coupling is associated with negative health outcomes. Krüppel-like factors (KLFs) are transcription factors that govern metabolic homeostasis in various organs. Many KLFs show a circadian expression in the liver. Here, we show that the loss of the clock-controlled KLF10 in hepatocytes results in extensive reprogramming of the mouse liver circadian transcriptome, which in turn alters the temporal coordination of pathways associated with energy metabolism. We also show that glucose and fructose induce Klf10, which helps mitigate glucose intolerance and hepatic steatosis in mice challenged with a sugar beverage. Functional genomics further reveal that KLF10 target genes are primarily involved in central carbon metabolism. Together, these findings show that in the liver KLF10 integrates circadian timing and sugar metabolism-related signaling, and serves as a transcriptional brake that protects against the deleterious effects of increased sugar consumption. |
format | Online Article Text |
id | pubmed-8410083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-84100832021-09-03 KLF10 integrates circadian timing and sugar signaling to coordinate hepatic metabolism Ruberto, Anthony A Gréchez-Cassiau, Aline Guérin, Sophie Martin, Luc Revel, Johana S Mehiri, Mohamed Subramaniam, Malayannan Delaunay, Franck Teboul, Michèle eLife Cell Biology The mammalian circadian timing system and metabolism are highly interconnected, and disruption of this coupling is associated with negative health outcomes. Krüppel-like factors (KLFs) are transcription factors that govern metabolic homeostasis in various organs. Many KLFs show a circadian expression in the liver. Here, we show that the loss of the clock-controlled KLF10 in hepatocytes results in extensive reprogramming of the mouse liver circadian transcriptome, which in turn alters the temporal coordination of pathways associated with energy metabolism. We also show that glucose and fructose induce Klf10, which helps mitigate glucose intolerance and hepatic steatosis in mice challenged with a sugar beverage. Functional genomics further reveal that KLF10 target genes are primarily involved in central carbon metabolism. Together, these findings show that in the liver KLF10 integrates circadian timing and sugar metabolism-related signaling, and serves as a transcriptional brake that protects against the deleterious effects of increased sugar consumption. eLife Sciences Publications, Ltd 2021-08-17 /pmc/articles/PMC8410083/ /pubmed/34402428 http://dx.doi.org/10.7554/eLife.65574 Text en © 2021, Ruberto et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Ruberto, Anthony A Gréchez-Cassiau, Aline Guérin, Sophie Martin, Luc Revel, Johana S Mehiri, Mohamed Subramaniam, Malayannan Delaunay, Franck Teboul, Michèle KLF10 integrates circadian timing and sugar signaling to coordinate hepatic metabolism |
title | KLF10 integrates circadian timing and sugar signaling to coordinate hepatic metabolism |
title_full | KLF10 integrates circadian timing and sugar signaling to coordinate hepatic metabolism |
title_fullStr | KLF10 integrates circadian timing and sugar signaling to coordinate hepatic metabolism |
title_full_unstemmed | KLF10 integrates circadian timing and sugar signaling to coordinate hepatic metabolism |
title_short | KLF10 integrates circadian timing and sugar signaling to coordinate hepatic metabolism |
title_sort | klf10 integrates circadian timing and sugar signaling to coordinate hepatic metabolism |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410083/ https://www.ncbi.nlm.nih.gov/pubmed/34402428 http://dx.doi.org/10.7554/eLife.65574 |
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