Control of mitochondrial integrity in ageing and disease

被引:50
作者
Szklarczyk, Radek [1 ,3 ]
Nooteboom, Marco [2 ]
Osiewacz, Heinz D. [4 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Ctr Mol & Biomol Informat, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Dept Biochem 286, NL-6500 HB Nijmegen, Netherlands
[3] Maastricht Univ, Med Ctr, Unit Clin Genom, Dept Clin Genet, NL-6200 MD Maastricht, Netherlands
[4] Goethe Univ Frankfurt, Fac Biosci & Cluster Excellence Macromol Complexe, D-60438 Frankfurt, Germany
关键词
mitochondria; quality control; disease; ageing; M-AAA PROTEASE; DNA-POLYMERASE-GAMMA; DYNAMIN-RELATED PROTEIN; DOMINANT OPTIC ATROPHY; BASE EXCISION-REPAIR; PLASMID-LIKE DNA; SPASTIC PARAPLEGIA; METHIONINE SULFOXIDE; POINT MUTATIONS; QUALITY-CONTROL;
D O I
10.1098/rstb.2013.0439
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Various molecular and cellular pathways are active in eukaryotes to control the quality and integrity of mitochondria. These pathways are involved in keeping a 'healthy' population of this essential organelle during the lifetime of the organism. Quality control (QC) systems counteract processes that lead to organellar dysfunction manifesting as degenerative diseases and ageing. We discuss disease-and ageing-related pathways involved in mitochondrial QC: mtDNA repair and reorganization, regeneration of oxidized amino acids, refolding and degradation of severely damaged proteins, degradation of whole mitochondria by mitophagy and finally programmed cell death. The control of the integrity of mtDNA and regulation of its expression is essential to remodel single proteins as well as mitochondrial complexes that determine mitochondrial functions. The redundancy of components, such as proteases, and the hierarchies of the QC raise questions about crosstalk between systems and their precise regulation. The understanding of the underlying mechanisms on the genomic, proteomic, organellar and cellular levels holds the key for the development of interventions for mitochondrial dysfunctions, degenerative processes, ageing and age-related diseases resulting from impairments of mitochondria.
引用
收藏
页数:18
相关论文
共 249 条
  • [1] Biological Roles of the Podospora anserina Mitochondrial Lon Protease and the Importance of Its N-Domain
    Adam, Celine
    Picard, Marguerite
    Dequard-Chablat, Michelle
    Sellem, Carole H.
    Hermann-Le Denmat, Sylvie
    Contamine, Veronique
    [J]. PLOS ONE, 2012, 7 (05):
  • [2] Bioenergetics and the formation of mitochondrial reactive oxygen species
    Adam-Vizi, Vera
    Chinopoulos, Christos
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2006, 27 (12) : 639 - 645
  • [3] Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74
    Ahmed, Zubair M.
    Yousaf, Rizwan
    Lee, Byung Cheon
    Khan, Shaheen N.
    Lee, Sue
    Lee, Kwanghyuk
    Husnain, Tayyab
    Rehman, Atteeq Ur
    Bonneux, Sarah
    Ansar, Muhammad
    Ahmad, Wasim
    Leal, Suzanne M.
    Gladyshev, Vadim N.
    Belyantseva, Inna A.
    Van Camp, Guy
    Riazuddin, Sheikh
    Friedman, Thomas B.
    Riazuddin, Saima
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2011, 88 (01) : 19 - 29
  • [4] Neuromuscular disease presentation with three genetic defects involving two genomes
    Al-Dosary, Mazhor
    Whittaker, Roger G.
    Haughton, Joanna
    McFarland, Robert
    Goodship, Judith
    Turnbull, Douglass M.
    Taylor, Robert W.
    [J]. NEUROMUSCULAR DISORDERS, 2009, 19 (12) : 841 - 844
  • [5] OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
    Alexander, C
    Votruba, M
    Pesch, UEA
    Thiselton, DL
    Mayer, S
    Moore, A
    Rodriguez, M
    Kellner, U
    Leo-Kottler, B
    Auburger, G
    Bhattacharya, SS
    Wissinger, B
    [J]. NATURE GENETICS, 2000, 26 (02) : 211 - 215
  • [6] AFG3L2 supports mitochondrial protein synthesis and Purkinje cell survival
    Almajan, Eva R.
    Richter, Ricarda
    Paeger, Lars
    Martinelli, Paola
    Barth, Esther
    Decker, Thorsten
    Larsson, Nils-Goeran
    Kloppenburg, Peter
    Langer, Thomas
    Rugarli, Elena I.
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (11) : 4048 - 4058
  • [7] OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes
    Amati-Bonneau, Patrizia
    Valentino, Maria Lucia
    Reynier, Pascal
    Gallardo, Maria Esther
    Bornstein, Belen
    Boissiere, Anne
    Campos, Yolanda
    Rivera, Henry
    de la Aleja, Jesus Gonzalez
    Carroccia, Rosanna
    Iommarini, Luisa
    Labauge, Pierre
    Figarella-Branger, Dominique
    Marcorelles, Pascale
    Furby, Alain
    Beauvais, Katell
    Letournel, Franck
    Liguori, Rocco
    La Morgia, Chiara
    Montagna, Pasquale
    Liguori, Maria
    Zanna, Claudia
    Rugolo, Michela
    Cossarizza, Andrea
    Wissinger, Bernd
    Verny, Christophe
    Schwarzenbacher, Robert
    Martin, Miguel Angel
    Arenas, Joaquin
    Ayuso, Carmen
    Garesse, Rafael
    Lenaers, Guy
    Bonneau, Dominique
    Carelli, Valerio
    [J]. BRAIN, 2008, 131 : 338 - 351
  • [8] [Anonymous], COLD SPRING HARB PER
  • [9] Membrane protein degradation by AAA proteases in mitochondria
    Arnold, I
    Langer, T
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2002, 1592 (01): : 89 - 96
  • [10] A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia
    Arnoldi, Alessia
    Tonelli, Alessandra
    Crippa, Francesca
    Villani, Gaetano
    Pacelli, Consiglia
    Sironi, Manuela
    Pozzoli, Uberto
    D'Angelo, Maria Grazia
    Meola, Giovanni
    Martinuzzi, Andrea
    Crimella, Claudia
    Redaelli, Francesca
    Panzeri, Chris
    Renieri, Alessandra
    Comi, Giacomo Pietro
    Turconi, Anna Carla
    Bresolin, Nereo
    Bassi, Maria Teresa
    [J]. HUMAN MUTATION, 2008, 29 (04) : 522 - 531