Methylation deficiency disrupts biological rhythms from bacteria to humans
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Published:2020-05-06
Issue:1
Volume:3
Page:
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ISSN:2399-3642
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Container-title:Communications Biology
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language:en
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Short-container-title:Commun Biol
Author:
Fustin Jean-MichelORCID, Ye Shiqi, Rakers ChristinORCID, Kaneko Kensuke, Fukumoto Kazuki, Yamano Mayu, Versteven Marijke, Grünewald Ellen, Cargill Samantha J., Tamai T. KatherineORCID, Xu Yao, Jabbur Maria Luísa, Kojima Rika, Lamberti Melisa L., Yoshioka-Kobayashi Kumiko, Whitmore DavidORCID, Tammam Stephanie, Howell P. LynneORCID, Kageyama Ryoichiro, Matsuo Takuya, Stanewsky RalfORCID, Golombek Diego A., Johnson Carl Hirschie, Kakeya HideakiORCID, van Ooijen GerbenORCID, Okamura Hitoshi
Abstract
AbstractThe methyl cycle is a universal metabolic pathway providing methyl groups for the methylation of nuclei acids and proteins, regulating all aspects of cellular physiology. We have previously shown that methyl cycle inhibition in mammals strongly affects circadian rhythms. Since the methyl cycle and circadian clocks have evolved early during evolution and operate in organisms across the tree of life, we sought to determine whether the link between the two is also conserved. Here, we show that methyl cycle inhibition affects biological rhythms in species ranging from unicellular algae to humans, separated by more than 1 billion years of evolution. In contrast, the cyanobacterial clock is resistant to methyl cycle inhibition, although we demonstrate that methylations themselves regulate circadian rhythms in this organism. Mammalian cells with a rewired bacteria-like methyl cycle are protected, like cyanobacteria, from methyl cycle inhibition, providing interesting new possibilities for the treatment of methylation deficiencies.
Publisher
Springer Science and Business Media LLC
Subject
General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)
Reference74 articles.
1. Cantoni, G. L. The role of S-adenosylhomocysteine in the biological utilization of S-adenosylmethionine. Prog. Clin. Biol. Res. 198, 47–65 (1985). 2. Chiang, P. K. & Cantoni, G. L. Perturbation of biochemical transmethylations by 3-deazaadenosine in vivo. Biochem. Pharmacol. 28, 1897–1902 (1979). 3. Hoffman, D. R., Marion, D. W., Cornatzer, W. E. & Duerre, J. A. S-Adenosylmethionine and S-adenosylhomocystein metabolism in isolated rat liver. Effects of L-methionine, L-homocystein, and adenosine. J. Biol. Chem. 255, 10822–10827 (1980). 4. Poirier, L. A., Herrera, L. A. C. & Wise, C. On the Chemical Causation of Methyl Deficiency and its Attendant Pathologies (2003). 5. Takahashi, J. S. In A Time for Metabolism and Hormones (Sassone-Corsi, P. & Christen, Y. eds.) 13–24 (The Author(s), Cham (CH), 2016).
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