Methylation deficiency disrupts biological rhythms from bacteria to humans
The 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 c...
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creator | Fustin, Jean-Michel Ye, Shiqi Rakers, Christin Kaneko, Kensuke Fukumoto, Kazuki Yamano, Mayu Versteven, Marijke Grünewald, Ellen Cargill, Samantha J. Tamai, T. Katherine Xu, Yao Jabbur, Maria Luísa Kojima, Rika Lamberti, Melisa L. Yoshioka-Kobayashi, Kumiko Whitmore, David Tammam, Stephanie Howell, P. Lynne Kageyama, Ryoichiro Matsuo, Takuya Stanewsky, Ralf Golombek, Diego A. Johnson, Carl Hirschie Kakeya, Hideaki van Ooijen, Gerben Okamura, Hitoshi |
description | The 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.
Fustin et al. reveal the evolutionarily conserved link between methyl metabolism and biological clocks. This study suggests the possibility of translating fundamental understanding of methylation deficiencies to clinical applications. |
doi_str_mv | 10.1038/s42003-020-0942-0 |
format | Article |
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Fustin et al. reveal the evolutionarily conserved link between methyl metabolism and biological clocks. This study suggests the possibility of translating fundamental understanding of methylation deficiencies to clinical applications.</description><identifier>ISSN: 2399-3642</identifier><identifier>EISSN: 2399-3642</identifier><identifier>DOI: 10.1038/s42003-020-0942-0</identifier><identifier>PMID: 32376902</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/1 ; 13/109 ; 13/44 ; 13/51 ; 14 ; 14/5 ; 38 ; 38/71 ; 38/90 ; 42 ; 59 ; 631/181 ; 631/443/319 ; 631/80/105 ; 64 ; 64/11 ; 64/116 ; 64/24 ; 64/60 ; 82/29 ; 82/58 ; 96 ; Algae ; Animals ; Arabidopsis - physiology ; Bacteria ; Biological clocks ; Biological rhythms ; Biology ; Biomedical and Life Sciences ; Caenorhabditis elegans - physiology ; Chlamydomonas reinhardtii - physiology ; Chlorophyta - physiology ; Circadian Rhythm ; Circadian rhythms ; Drosophila melanogaster - physiology ; Evolution ; Humans ; Life Sciences ; Mammalian cells ; Mammals ; Metabolic pathways ; Methylation ; Mice - physiology ; Synechococcus - physiology ; Therapeutic applications ; Zebrafish - physiology</subject><ispartof>Communications biology, 2020-05, Vol.3 (1), p.211-211, Article 211</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. 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Katherine</creatorcontrib><creatorcontrib>Xu, Yao</creatorcontrib><creatorcontrib>Jabbur, Maria Luísa</creatorcontrib><creatorcontrib>Kojima, Rika</creatorcontrib><creatorcontrib>Lamberti, Melisa L.</creatorcontrib><creatorcontrib>Yoshioka-Kobayashi, Kumiko</creatorcontrib><creatorcontrib>Whitmore, David</creatorcontrib><creatorcontrib>Tammam, Stephanie</creatorcontrib><creatorcontrib>Howell, P. Lynne</creatorcontrib><creatorcontrib>Kageyama, Ryoichiro</creatorcontrib><creatorcontrib>Matsuo, Takuya</creatorcontrib><creatorcontrib>Stanewsky, Ralf</creatorcontrib><creatorcontrib>Golombek, Diego A.</creatorcontrib><creatorcontrib>Johnson, Carl Hirschie</creatorcontrib><creatorcontrib>Kakeya, Hideaki</creatorcontrib><creatorcontrib>van Ooijen, Gerben</creatorcontrib><creatorcontrib>Okamura, Hitoshi</creatorcontrib><title>Methylation deficiency disrupts biological rhythms from bacteria to humans</title><title>Communications biology</title><addtitle>Commun Biol</addtitle><addtitle>Commun Biol</addtitle><description>The 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.
Fustin et al. reveal the evolutionarily conserved link between methyl metabolism and biological clocks. 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subjects | 13/1 13/109 13/44 13/51 14 14/5 38 38/71 38/90 42 59 631/181 631/443/319 631/80/105 64 64/11 64/116 64/24 64/60 82/29 82/58 96 Algae Animals Arabidopsis - physiology Bacteria Biological clocks Biological rhythms Biology Biomedical and Life Sciences Caenorhabditis elegans - physiology Chlamydomonas reinhardtii - physiology Chlorophyta - physiology Circadian Rhythm Circadian rhythms Drosophila melanogaster - physiology Evolution Humans Life Sciences Mammalian cells Mammals Metabolic pathways Methylation Mice - physiology Synechococcus - physiology Therapeutic applications Zebrafish - physiology |
title | Methylation deficiency disrupts biological rhythms from bacteria to humans |
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