TY - JOUR
T1 - Mitochondrial stress response triggered by defects in protein synthesis quality control
AU - Richter, Uwe
AU - Ng, Kah Ying
AU - Suomi, Fumi
AU - Marttinen, Paula
AU - Turunen, Taina
AU - Jackson, Christopher
AU - Suomalainen, Anu
AU - Vihinen, Helena
AU - Jokitalo, Eija
AU - Nyman, Tuula A
AU - Isokallio, Marita A
AU - Stewart, James B
AU - Mancini, Cecilia
AU - Brusco, Alfredo
AU - Seneca, Sara
AU - Lombès, Anne
AU - Taylor, Robert W
AU - Battersby, Brendan J
N1 - © 2019 Richter et al.
PY - 2019/2
Y1 - 2019/2
N2 - 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.
AB - 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.
KW - ATP-Dependent Proteases/genetics
KW - ATPases Associated with Diverse Cellular Activities/genetics
KW - Animals
KW - Fibroblasts/metabolism
KW - GTP Phosphohydrolases/metabolism
KW - Gene Knockdown Techniques
KW - HEK293 Cells
KW - Humans
KW - Metalloendopeptidases/metabolism
KW - Mice
KW - Mitochondria/metabolism
KW - Mitochondrial Membranes/metabolism
KW - Mitochondrial Proteins/biosynthesis
KW - Mitochondrial Ribosomes/metabolism
KW - Mutation
KW - Phenotype
KW - Protein Biosynthesis
KW - RNA, Messenger/genetics
KW - RNA, Small Interfering/genetics
KW - Transfection
UR - http://www.scopus.com/inward/record.url?scp=85060804414&partnerID=8YFLogxK
U2 - 10.26508/lsa.201800219
DO - 10.26508/lsa.201800219
M3 - Article
C2 - 30683687
VL - 2
JO - Life science alliance
JF - Life science alliance
SN - 2575-1077
IS - 1
M1 - e201800219
ER -