| Literature DB >> 27033304 |
Marcello Pinti1, Lara Gibellini2, Milena Nasi2, Sara De Biasi2, Carlo Augusto Bortolotti1, Anna Iannone3, Andrea Cossarizza4.
Abstract
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.Entities:
Keywords: CODAS syndrome; Cancer; Chaperone; Lon; Mitochondria; Protease; mtDNA
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Year: 2016 PMID: 27033304 DOI: 10.1016/j.bbabio.2016.03.025
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002