Mitochondrial stress response triggered by defects in protein synthesis quality control

被引:29
|
作者
Richter, Uwe [1 ]
Ng, Kah Ying [1 ]
Suomi, Fumi [1 ]
Marttinen, Paula [1 ]
Turunen, Taina [1 ]
Jackson, Christopher [2 ]
Suomalainen, Anu [2 ]
Vihinen, Helena [1 ]
Jokitalo, Eija [1 ]
Nyman, Tuula A. [3 ,4 ]
Isokallio, Marita A. [5 ]
Stewart, James B. [5 ]
Mancini, Cecilia [6 ]
Brusco, Alfredo [6 ]
Seneca, Sara [7 ]
Lombes, Anne [8 ]
Taylor, Robert W. [9 ]
Battersby, Brendan J. [1 ]
机构
[1] Univ Helsinki, Inst Biotechnol, Helsinki, Finland
[2] Univ Helsinki, Res Programs Unit Mol Neurol, Helsinki, Finland
[3] Univ Oslo, Inst Clin Med, Dept Immunol, Oslo, Norway
[4] Oslo Univ Hosp, Oslo, Norway
[5] Max Planck Inst Biol Ageing, Cologne, Germany
[6] Univ Torino, Dept Med Sci, Turin, Italy
[7] Univ Ziekenhuis Brussel, Res Ctr Reprod & Genet, Ctr Med Genet, Brussels, Belgium
[8] Univ Paris 05, CNRS, INSERM, Fac Med Cochin,Inst Cochin,U1016,UMR 8104, Paris, France
[9] Newcastle Univ, Inst Neurosci, Wellcome Ctr Mitochondrial Res, Newcastle Upon Tyne, Tyne & Wear, England
基金
芬兰科学院; 英国医学研究理事会;
关键词
M-AAA PROTEASE; COMPUTATIONAL PLATFORM; SPASTIC PARAPLEGIA; READ ALIGNMENT; DNA DELETIONS; MUTATIONS; OPA1; MEMBRANE; ATAXIA; TURNOVER;
D O I
10.26508/lsa.201800219
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mitochondria have a compartmentalized gene expression system dedicated to the synthesis of membrane proteins essential for oxidative phosphorylation. Responsive quality control mechanisms are needed to ensure that aberrant protein synthesis does not disrupt mitochondrial function. Pathogenic mutations that impede the function of the mitochondrial matrix quality control protease complex composed of AFG3L2 and paraplegin cause a multifaceted clinical syndrome. At the cell and molecular level, defects to this quality control complex are defined by impairment to mitochondrial form and function. Here, we establish the etiology of these phenotypes. We show how disruptions to the quality control of mitochondrial protein synthesis trigger a sequential stress response characterized first by OMA1 activation followed by loss of mitochondrial ribosomes and by remodelling of mitochondrial inner membrane ultrastructure. Inhibiting mitochondrial protein synthesis with chloramphenicol completely blocks this stress response. Together, our data establish a mechanism linking major cell biological phenotypes of AFG3L2 pathogenesis and show how modulation of mitochondrial protein synthesis can exert a beneficial effect on organelle homeostasis.
引用
收藏
页数:17
相关论文
共 50 条
  • [41] Oxidative stress, mitochondrial dysfunction, and respiratory chain enzyme defects in inflammatory myopathies
    Danieli, Maria Giovanna
    Antonelli, Eleonora
    Piga, Mario Andrea
    Cozzi, Maria Francesca
    Allegra, Alessandro
    Gangemi, Sebastiano
    AUTOIMMUNITY REVIEWS, 2023, 22 (02)
  • [42] Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency
    Leman, Geraldine
    Gueguen, Naig
    Desquiret-Dumas, Valerie
    Kane, Mariame Selma
    Wettervald, Celine
    Chupin, Stephanie
    Chevrollier, Arnaud
    Lebre, Anne-Sophie
    Bonnefont, Jean-Paul
    Barth, Magalie
    Amati-Bonneau, Patrizia
    Verny, Christophe
    Henrion, Daniel
    Bonneau, Dominique
    Reynier, Pascal
    Procaccio, Vincent
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2015, 65 : 91 - 103
  • [43] Condensin II protein dysfunction impacts mitochondrial respiration and mitochondrial oxidative stress responses
    Deutschman, Emily
    Ward, Jacqueline R.
    Kumar, Avinash
    Ray, Greeshma
    Welch, Nicole
    Lemieux, Madeleine E.
    Dasarathy, Srinivisan
    Longworth, Michelle S.
    JOURNAL OF CELL SCIENCE, 2019, 132 (22)
  • [44] mTORC1 Regulates Mitochondrial Integrated Stress Response and Mitochondrial Myopathy Progression
    Khan, Nahid A.
    Nikkanen, Joni
    Yatsuga, Shuichi
    Jackson, Christopher
    Wang, Liya
    Pradhan, Swagat
    Kivela, Riikka
    Pessia, Alberto
    Velagapudi, Vidya
    Suomalainen, Anu
    CELL METABOLISM, 2017, 26 (02) : 419 - +
  • [45] Mitochondrial Protein Synthesis Adapts to Influx of Nuclear-Encoded Protein
    Richter-Dennerlein, Ricarda
    Oeljeklaus, Silke
    Lorenzi, Isotta
    Ronsoer, Christin
    Bareth, Bettina
    Schendzielorz, Alexander Benjamin
    Wang, Cong
    Warscheid, Bettina
    Rehling, Peter
    Dennerlein, Sven
    CELL, 2016, 167 (02) : 471 - +
  • [46] Mitochondrial quality control: a matter of life and death for neurons
    Rugarli, Elena I.
    Langer, Thomas
    EMBO JOURNAL, 2012, 31 (06) : 1336 - 1349
  • [47] Translation matters: protein synthesis defects in inherited disease
    Scheper, Gert C.
    van der Knaap, Marjo S.
    Proud, Christopher G.
    NATURE REVIEWS GENETICS, 2007, 8 (09) : 711 - 723
  • [48] Amyotrophic Lateral Sclerosis, FUS and Protein Synthesis Defects
    Assoni, Amanda Faria
    Foijer, Floris
    Zatz, Mayana
    STEM CELL REVIEWS AND REPORTS, 2023, 19 (03) : 625 - 638
  • [49] Intracellular quality control of mitochondrial DNA: evidence and limitations
    Knorre, Dmitry A.
    PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2020, 375 (1790)
  • [50] Translation of MT-ATP6 pathogenic variants reveals distinct regulatory consequences from the co-translational quality control of mitochondrial protein synthesis
    Ng, Kah Ying
    Richter, Uwe
    Jackson, Christopher B.
    Seneca, Sara
    Battersby, Brendan J.
    HUMAN MOLECULAR GENETICS, 2022, 31 (08) : 1230 - 1241