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Methylation deficiency disrupts biological rhythms from bacteria to humans.

Authors :
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
Source :
Communications Biology; 5/6/2020, Vol. 3 Issue 1, p1-14, 14p
Publication Year :
2020

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. 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
23993642
Volume :
3
Issue :
1
Database :
Complementary Index
Journal :
Communications Biology
Publication Type :
Academic Journal
Accession number :
143073955
Full Text :
https://doi.org/10.1038/s42003-020-0942-0