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The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells
by
Hamon-Keromen, E.
, Gautier, C. A.
, Mannoury la Cour, C.
, Harper, J. W.
, Boutin, J. A.
, Millan, M. J.
, Guedin, D.
, Jacoupy, M.
, Corti, O.
, Coge, F.
, Corvol, J.-C.
, Brice, A.
, Nosjean, O.
, Ordureau, A.
, Erpapazoglou, Z.
in
13/109
/ 13/56
/ 13/89
/ 14/34
/ 14/35
/ 14/5
/ 14/63
/ 631/378/1689/1718
/ 631/80/304
/ 631/80/642/333
/ 82/1
/ 82/29
/ 82/80
/ Alzheimer's disease
/ Biosensing Techniques
/ Biosensors
/ Biosynthesis
/ Cytosol
/ Dehydrogenases
/ Efficiency
/ HEK293 Cells
/ Humanities and Social Sciences
/ Humans
/ Life Sciences
/ Mitochondria
/ Mitochondrial Proteins - metabolism
/ multidisciplinary
/ Parkin protein
/ Parkinson's disease
/ Pathophysiology
/ Protein Kinases - metabolism
/ Protein Transport
/ Proteins
/ PTEN-induced putative kinase
/ Regulation
/ Science
/ Science (multidisciplinary)
/ Translocase
/ Ubiquitin
/ Ubiquitin-protein ligase
/ Ubiquitin-Protein Ligases - metabolism
2019
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The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells
by
Hamon-Keromen, E.
, Gautier, C. A.
, Mannoury la Cour, C.
, Harper, J. W.
, Boutin, J. A.
, Millan, M. J.
, Guedin, D.
, Jacoupy, M.
, Corti, O.
, Coge, F.
, Corvol, J.-C.
, Brice, A.
, Nosjean, O.
, Ordureau, A.
, Erpapazoglou, Z.
in
13/109
/ 13/56
/ 13/89
/ 14/34
/ 14/35
/ 14/5
/ 14/63
/ 631/378/1689/1718
/ 631/80/304
/ 631/80/642/333
/ 82/1
/ 82/29
/ 82/80
/ Alzheimer's disease
/ Biosensing Techniques
/ Biosensors
/ Biosynthesis
/ Cytosol
/ Dehydrogenases
/ Efficiency
/ HEK293 Cells
/ Humanities and Social Sciences
/ Humans
/ Life Sciences
/ Mitochondria
/ Mitochondrial Proteins - metabolism
/ multidisciplinary
/ Parkin protein
/ Parkinson's disease
/ Pathophysiology
/ Protein Kinases - metabolism
/ Protein Transport
/ Proteins
/ PTEN-induced putative kinase
/ Regulation
/ Science
/ Science (multidisciplinary)
/ Translocase
/ Ubiquitin
/ Ubiquitin-protein ligase
/ Ubiquitin-Protein Ligases - metabolism
2019
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The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells
by
Hamon-Keromen, E.
, Gautier, C. A.
, Mannoury la Cour, C.
, Harper, J. W.
, Boutin, J. A.
, Millan, M. J.
, Guedin, D.
, Jacoupy, M.
, Corti, O.
, Coge, F.
, Corvol, J.-C.
, Brice, A.
, Nosjean, O.
, Ordureau, A.
, Erpapazoglou, Z.
in
13/109
/ 13/56
/ 13/89
/ 14/34
/ 14/35
/ 14/5
/ 14/63
/ 631/378/1689/1718
/ 631/80/304
/ 631/80/642/333
/ 82/1
/ 82/29
/ 82/80
/ Alzheimer's disease
/ Biosensing Techniques
/ Biosensors
/ Biosynthesis
/ Cytosol
/ Dehydrogenases
/ Efficiency
/ HEK293 Cells
/ Humanities and Social Sciences
/ Humans
/ Life Sciences
/ Mitochondria
/ Mitochondrial Proteins - metabolism
/ multidisciplinary
/ Parkin protein
/ Parkinson's disease
/ Pathophysiology
/ Protein Kinases - metabolism
/ Protein Transport
/ Proteins
/ PTEN-induced putative kinase
/ Regulation
/ Science
/ Science (multidisciplinary)
/ Translocase
/ Ubiquitin
/ Ubiquitin-protein ligase
/ Ubiquitin-Protein Ligases - metabolism
2019
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The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells
Journal Article
The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells
2019
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Overview
Most of over a thousand mitochondrial proteins are encoded by nuclear genes and must be imported from the cytosol. Little is known about the cytosolic events regulating mitochondrial protein import, partly due to the lack of appropriate tools for its assessment in living cells. We engineered an inducible biosensor for monitoring the main presequence-mediated import pathway with a quantitative, luminescence-based readout. This tool was used to explore the regulation of mitochondrial import by the PINK1 kinase-driven Parkin ubiquitin ligase, which is dysfunctional in autosomal recessive Parkinson’s disease. We show that mitochondrial import was stimulated by Parkin, but not by disease-causing Parkin variants. This effect was dependent on Parkin activation by PINK1 and accompanied by an increase in the abundance of K11 ubiquitin chains on mitochondria and by ubiquitylation of subunits of the translocase of outer mitochondrial membrane. Mitochondrial import efficiency was abnormally low in cells from patients with
PINK1-
and
PARK2
-linked Parkinson’s disease and was restored by phosphomimetic ubiquitin in cells with residual Parkin activity. Altogether, these findings uncover a role of ubiquitylation in mitochondrial import regulation and suggest that loss of this regulatory loop may underlie the pathophysiology of Parkinson’s disease, providing novel opportunities for therapeutic intervention.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 13/56
/ 13/89
/ 14/34
/ 14/35
/ 14/5
/ 14/63
/ 82/1
/ 82/29
/ 82/80
/ Cytosol
/ Humanities and Social Sciences
/ Humans
/ Mitochondrial Proteins - metabolism
/ Protein Kinases - metabolism
/ Proteins
/ PTEN-induced putative kinase
/ Science
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