The methyl cycle is a conserved regulator of biological clocks

Author:

Fustin Jean-MichelORCID,Ye Shiqi,Rakers Christin,Versteven Marijke,Cargill Samantha J.,Tamai T. Katherine,Xu Yao,Jabbur Maria Luísa,Kojima Rika,Lamberti Melisa L.,Yoshioka-Kobayashi Kumiko,Whitmore David,Kageyama Ryoichiro,Matsuo Takuya,Stanewsky RalfORCID,Golombek Diego A.,Johnson Carl Hirschie,van Ooijen Gerben,Okamura Hitoshi

Abstract

AbstractThe methyl cycle is a universally conserved metabolic pathway operating in prokaryotes and eukaryotes. In this pathway, the amino acid methionine is used to synthesize S-adenosylmethionine, the methyl donor co-substrate in the methylation of nucleic acids, histone and non-histone proteins and many other molecules within the cell. The methylation of nucleic acids and proteins is the foundation of epigenetic and epitranscriptomic regulations of gene expression, but whether the methyl cycle centrally regulates gene expression and function by controlling the availability of methyl moieties is poorly understood.From cyanobacteria to humans, a circadian clock that involves an exquisitely regulated transcription-translation-feedback loop driving oscillations in gene expression and orchestrating physiology and behavior has been described. We reported previously that inhibition of the methyl cycle in mammalian cells caused the lengthening of the period of these oscillations, suggesting the methyl cycle may indeed act as a central regulator of gene expression, at least in mammals. Here, we investigated whether the methyl cycle, given its universal presence among living beings, regulates the circadian clock in species across the phylogenetic tree of life.We reveal a remarkable evolutionary conservation of the link between the methyl cycle and the circadian clock. Moreover, we show that the methyl cycle also regulates the somite segmentation clock, another transcription-translation negative feedback loop-based timing mechanism that orchestrate embryonic development in vertebrates, highlighting the methyl cycle as a master regulator of biological clocks.SIGNIFICANCE STATEMENTHere we reveal that the methyl cycle, a universal metabolic pathway leading to the synthesis of S-adenosylmethionine, the methyl donor co-substrate in virtually all transmethylation reactions within the cell, is a conserved regulator of biological clocks. These discoveries highlight the methyl cycle as a metabolic hub that regulates gene expression via the availability of methyl moieties for the methylation of nucleic acids, proteins and many other molecules with the cell.

Publisher

Cold Spring Harbor Laboratory

Reference75 articles.

1. Hyperhomocysteinemia in health and disease: Where we are now, and where do we go from here ?;Clin Chem Lab Med,2012

2. The role of S-adenosylhomocysteine in the biological utilization of S-adenosylmethionine;Prog Clin Biol Res,1985

3. Perturbation of biochemical transmethylations by 3-deazaadenosine in vivo

4. S-adenosylmethionine and S-adenosylhomocystein metabolism in isolated rat liver. effects of L-methionine, L-homocystein, and adenosine;J Biol Chem,1980

5. Rana AK & Ankri S (2016) Reviving the RNA world: An insight into the appearance of RNA methyltransferases. Front Genet 7: 99.

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