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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
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Tammam, Stephanie
dc.contributor.author
Howell, P. Lynne
dc.contributor.author
Kageyama, Ryoichiro
dc.contributor.author
Matsuo, Takuya
dc.contributor.author
Stanewsky, Ralf
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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
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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
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