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dc.contributor.author
Fustin, Jean Michel  
dc.contributor.author
Ye, Shiqi  
dc.contributor.author
Rakers, Christin  
dc.contributor.author
Kaneko, Kensuke  
dc.contributor.author
Fukumoto, Kazuki  
dc.contributor.author
Yamano, Mayu  
dc.contributor.author
Versteven, Marijke  
dc.contributor.author
Grünewald, Ellen  
dc.contributor.author
Cargill, Samantha J.  
dc.contributor.author
Tamai, T. Katherine  
dc.contributor.author
Xu, Yao  
dc.contributor.author
Jabbur, Maria Luísa  
dc.contributor.author
Kojima, Rika  
dc.contributor.author
Lamberti, Melisa Luciana  
dc.contributor.author
Yoshioka Kobayashi, Kumiko  
dc.contributor.author
Whitmore, David  
dc.contributor.author
Tammam, Stephanie  
dc.contributor.author
Howell, P. Lynne  
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Kageyama, Ryoichiro  
dc.contributor.author
Matsuo, Takuya  
dc.contributor.author
Stanewsky, Ralf  
dc.contributor.author
Golombek, Diego Andrés  
dc.contributor.author
Johnson, Carl Hirschie  
dc.contributor.author
Kakeya, Hideaki  
dc.contributor.author
Van Ooijen, Gerben  
dc.contributor.author
Okamura, Hitoshi  
dc.date.available
2022-09-20T00:57:50Z  
dc.date.issued
2020-06  
dc.identifier.citation
Fustin, Jean Michel; Ye, Shiqi; Rakers, Christin; Kaneko, Kensuke; Fukumoto, Kazuki; et al.; Methylation deficiency disrupts biological rhythms from bacteria to humans; Springer; Communications biology; 3; 1; 6-2020; 1-14  
dc.identifier.uri
http://hdl.handle.net/11336/169425  
dc.description.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.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Springer  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by/2.5/ar/  
dc.subject
Circadian rhythms  
dc.subject
Evolution  
dc.subject
Metabolism  
dc.subject
Methylation  
dc.subject.classification
Bioquímica y Biología Molecular  
dc.subject.classification
Ciencias Biológicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Methylation deficiency disrupts biological rhythms from bacteria to humans  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2022-09-19T14:54:29Z  
dc.identifier.eissn
2399-3642  
dc.journal.volume
3  
dc.journal.number
1  
dc.journal.pagination
1-14  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Londres  
dc.description.fil
Fil: Fustin, Jean Michel. Kyoto University; Japón. University of Manchester; Reino Unido  
dc.description.fil
Fil: Ye, Shiqi. Kyoto University; Japón  
dc.description.fil
Fil: Rakers, Christin. Kyoto University; Japón  
dc.description.fil
Fil: Kaneko, Kensuke. Kyoto University; Japón  
dc.description.fil
Fil: Fukumoto, Kazuki. Kyoto University; Japón  
dc.description.fil
Fil: Yamano, Mayu. Kyoto University; Japón  
dc.description.fil
Fil: Versteven, Marijke. University of Münster; Alemania  
dc.description.fil
Fil: Grünewald, Ellen. University of Edinburgh; Reino Unido  
dc.description.fil
Fil: Cargill, Samantha J.. University of Edinburgh; Reino Unido  
dc.description.fil
Fil: Tamai, T. Katherine. University of California at Los Angeles; Estados Unidos  
dc.description.fil
Fil: Xu, Yao. Vanderbilt University; Estados Unidos  
dc.description.fil
Fil: Jabbur, Maria Luísa. Vanderbilt University; Estados Unidos  
dc.description.fil
Fil: Kojima, Rika. Karolinska Huddinge Hospital. Karolinska Institutet; Suecia  
dc.description.fil
Fil: Lamberti, Melisa Luciana. Universidad Nacional de Quilmes. Departamento de Ciencia y Tecnología. Laboratorio de Cronobiología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Yoshioka Kobayashi, Kumiko. Kyoto University; Japón  
dc.description.fil
Fil: Whitmore, David. University College London; Estados Unidos  
dc.description.fil
Fil: Tammam, Stephanie. University Of Toronto. Hospital For Sick Children; Canadá  
dc.description.fil
Fil: Howell, P. Lynne. University Of Toronto. Hospital For Sick Children; Canadá  
dc.description.fil
Fil: Kageyama, Ryoichiro. Kyoto University; Japón  
dc.description.fil
Fil: Matsuo, Takuya. Nagoya University; Japón  
dc.description.fil
Fil: Stanewsky, Ralf. University of Münster; Alemania  
dc.description.fil
Fil: Golombek, Diego Andrés. Universidad Nacional de Quilmes. Departamento de Ciencia y Tecnología. Laboratorio de Cronobiología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Johnson, Carl Hirschie. Vanderbilt University; Estados Unidos  
dc.description.fil
Fil: Kakeya, Hideaki. Kyoto University; Japón  
dc.description.fil
Fil: Van Ooijen, Gerben. University of Edinburgh; Reino Unido  
dc.description.fil
Fil: Okamura, Hitoshi. Kyoto University; Japón  
dc.journal.title
Communications biology  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.nature.com/articles/s42003-020-0942-0  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1038/s42003-020-0942-0