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MacroH2A1.1 regulates mitochondrial respiration by limiting nuclear NAD(+) consumption

  • Datos identificativos

    Identificador: imarina:3113455
    Handle: http://hdl.handle.net/20.500.11797/imarina3113455
  • Autores:

    Marjanovic, Melanija Posavec
    Hurtado-Bages, Sarah
    Lassi, Maximilian
    Valero, Vanesa
    Malinverni, Roberto
    Delage, Helene
    Navarro, Miriam
    Corujo, David
    Guberovic, Iva
    Douet, Julien
    Gama-Perez, Pau
    Garcia-Roves, Pablo M.
    Ahel, Ivan
    Ladurner, Andreas G.
    Yanes, Oscar
    Bouvet, Philippe
    Suelves, Monica
    Teperino, Raffaele
    Pospisilik, J. Andrew
    Buschbeck, Marcus
  • Otros:

    Autor según el artículo: Marjanovic, Melanija Posavec; Hurtado-Bages, Sarah; Lassi, Maximilian; Valero, Vanesa; Malinverni, Roberto; Delage, Helene; Navarro, Miriam; Corujo, David; Guberovic, Iva; Douet, Julien; Gama-Perez, Pau; Garcia-Roves, Pablo M.; Ahel, Ivan; Ladurner, Andreas G.; Yanes, Oscar; Bouvet, Philippe; Suelves, Monica; Teperino, Raffaele; Pospisilik, J. Andrew; Buschbeck, Marcus;
    Departamento: Enginyeria Electrònica, Elèctrica i Automàtica
    Autor/es de la URV: Yanes Torrado, Óscar
    Palabras clave: Hashtag Etiqueta «#» @uroweb @residentesaeu @infoAeu
    Resumen: Histone variants are structural components of eukaryotic chromatin that can replace replication-coupled histones in the nucleosome. The histone variant macroH2A1.1 contains a macrodomain capable of binding NAD+-derived metabolites. Here we report that macroH2A1.1 is rapidly induced during myogenic differentiation through a switch in alternative splicing, and that myotubes that lack macroH2A1.1 have a defect in mitochondrial respiratory capacity. We found that the metabolite-binding macrodomain was essential for sustained optimal mitochondrial function but dispensable for gene regulation. Through direct binding, macroH2A1.1 inhibits basal poly-ADP ribose polymerase 1 (PARP-1) activity and thus reduces nuclear NAD+ consumption. The resultant accumulation of the NAD+ precursor NMN allows for maintenance of mitochondrial NAD+ pools that are critical for respiration. Our data indicate that macroH2A1.1-containing chromatin regulates mitochondrial respiration by limiting nuclear NAD+ consumption and establishing a buffer of NAD+ precursors in differentiated cells.
    Áreas temáticas: Structural biology Molecular biology Medicina ii General medicine Engenharias iv Ciências biológicas i Cell biology Biophysics Biochemistry & molecular biology
    Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 15459985
    Direcció de correo del autor: oscar.yanes@urv.cat
    Identificador del autor: 0000-0003-3695-7157
    Fecha de alta del registro: 2023-02-18
    Versión del articulo depositado: info:eu-repo/semantics/acceptedVersion
    Enlace a la fuente original: https://www.nature.com/articles/nsmb.3481
    URL Documento de licencia: http://repositori.urv.cat/ca/proteccio-de-dades/
    Referencia al articulo segun fuente origial: Nature Structural & Molecular Biology. 24 (11): 902-+
    Referencia de l'ítem segons les normes APA: Marjanovic, Melanija Posavec; Hurtado-Bages, Sarah; Lassi, Maximilian; Valero, Vanesa; Malinverni, Roberto; Delage, Helene; Navarro, Miriam; Corujo, D (2017). MacroH2A1.1 regulates mitochondrial respiration by limiting nuclear NAD(+) consumption. Nature Structural & Molecular Biology, 24(11), 902-+. DOI: 10.1038/nsmb.3481
    DOI del artículo: 10.1038/nsmb.3481
    Entidad: Universitat Rovira i Virgili
    Año de publicación de la revista: 2017
    Tipo de publicación: Journal Publications
  • Palabras clave:

    Biochemistry & Molecular Biology,Biophysics,Cell Biology,Molecular Biology,Structural Biology
    Structural biology
    Molecular biology
    Medicina ii
    General medicine
    Engenharias iv
    Ciências biológicas i
    Cell biology
    Biophysics
    Biochemistry & molecular biology
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