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Emerging role of Lon protease as a master regulator of mitochondrial functions.
Pinti, Marcello; Gibellini, Lara; Nasi, Milena; De Biasi, Sara; Bortolotti, Carlo Augusto; Iannone, Anna; Cossarizza, Andrea.
Afiliación
  • Pinti M; Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Gibellini L; Department of Surgery, Medicine, Dentistry and Morphological Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Nasi M; Department of Surgery, Medicine, Dentistry and Morphological Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • De Biasi S; Department of Surgery, Medicine, Dentistry and Morphological Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Bortolotti CA; Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
  • Iannone A; Department of Diagnostics, Clinical and Public Health Medicine, University of Modena and Reggio Emilia, Modena, Italy.
  • Cossarizza A; Department of Surgery, Medicine, Dentistry and Morphological Sciences, University of Modena and Reggio Emilia, Modena, Italy. Electronic address: andrea.cossarizza@unimore.it.
Biochim Biophys Acta ; 1857(8): 1300-1306, 2016 Aug.
Article en En | MEDLINE | ID: mdl-27033304
Lon protease is a nuclear-encoded, mitochondrial ATP-dependent protease highly conserved throughout the evolution, crucial for the maintenance of mitochondrial homeostasis. Lon acts as a chaperone of misfolded proteins, and is necessary for maintaining mitochondrial DNA. The impairment of these functions has a deep impact on mitochondrial functionality and morphology. An altered expression of Lon leads to a profound reprogramming of cell metabolism, with a switch from respiration to glycolysis, which is often observed in cancer cells. Mutations of Lon, which likely impair its chaperone properties, are at the basis of a genetic inherited disease named of the cerebral, ocular, dental, auricular, skeletal (CODAS) syndrome. This article is part of a Special Issue entitled 'EBEC 2016: 19th European Bioenergetics Conference, Riva del Garda, Italy, July 2-6, 2016', edited by Prof. Paolo Bernardi.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Osteocondrodisplasias / Anomalías Dentarias / ADN Mitocondrial / Anomalías del Ojo / Chaperonas Moleculares / Anomalías Craneofaciales / Proteasa La / Trastornos del Crecimiento / Luxación Congénita de la Cadera / Mitocondrias Límite: Humans Idioma: En Revista: Biochim Biophys Acta Año: 2016 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Osteocondrodisplasias / Anomalías Dentarias / ADN Mitocondrial / Anomalías del Ojo / Chaperonas Moleculares / Anomalías Craneofaciales / Proteasa La / Trastornos del Crecimiento / Luxación Congénita de la Cadera / Mitocondrias Límite: Humans Idioma: En Revista: Biochim Biophys Acta Año: 2016 Tipo del documento: Article País de afiliación: Italia