| Literature DB >> 32376902 |
Jean-Michel Fustin1,2, Shiqi Ye3, Christin Rakers4, Kensuke Kaneko5, Kazuki Fukumoto3, Mayu Yamano3, Marijke Versteven6, Ellen Grünewald7, Samantha J Cargill7, T Katherine Tamai8, Yao Xu9, Maria Luísa Jabbur9, Rika Kojima10, Melisa L Lamberti11, Kumiko Yoshioka-Kobayashi12, David Whitmore13, Stephanie Tammam14, P Lynne Howell14,15, Ryoichiro Kageyama12, Takuya Matsuo16, Ralf Stanewsky6, Diego A Golombek11, Carl Hirschie Johnson9, Hideaki Kakeya5, Gerben van Ooijen7, Hitoshi Okamura17,18.
Abstract
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.Entities:
Mesh:
Year: 2020 PMID: 32376902 PMCID: PMC7203018 DOI: 10.1038/s42003-020-0942-0
Source DB: PubMed Journal: Commun Biol ISSN: 2399-3642