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A long-lived pool of PINK1 imparts a molecular memory of depolarization-induced activity

The Parkinson’s disease-linked kinase, PINK1, is a short-lived protein that undergoes cleavage upon mitochondrial import leading to its proteasomal degradation. Under depolarizing conditions, it accumulates on mitochondria where it becomes activated, phosphorylating both ubiquitin and the ubiquitin...

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Hauptverfasser: Pollock, Liam (VerfasserIn) , Georgiou, Ioanna Ch. (VerfasserIn) , Rusilowicz-Jones, Emma V. (VerfasserIn) , Clague, Michael J. (VerfasserIn) , Urbé, Sylvie (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 28 Feb 2025
In: Science advances
Year: 2025, Jahrgang: 11, Heft: 9, Pages: 1-11
ISSN:2375-2548
DOI:10.1126/sciadv.adr1938
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.1126/sciadv.adr1938
Verlag, kostenfrei, Volltext: https://www.science.org/doi/10.1126/sciadv.adr1938
Volltext
Verfasserangaben:Liam Pollock, Ioanna Ch. Georgiou, Emma V. Rusilowicz-Jones, Michael J. Clague, Sylvie Urbé
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Zusammenfassung:The Parkinson’s disease-linked kinase, PINK1, is a short-lived protein that undergoes cleavage upon mitochondrial import leading to its proteasomal degradation. Under depolarizing conditions, it accumulates on mitochondria where it becomes activated, phosphorylating both ubiquitin and the ubiquitin E3 ligase Parkin, at Ser65. Our experiments reveal that in retinal pigment epithelial cells, only a fraction of PINK1 becomes stabilized after depolarization by electron transport chain inhibitors. Furthermore, the observed accrual of PINK1 cannot be completely accounted for without an accompanying increase in biosynthesis. We have used a ubiquitylation inhibitor TAK-243 to accumulate cleaved PINK1. Under these conditions, generation of unconjugated “free” phospho-ubiquitin serves as a proxy readout for PINK1 activity. This has enabled us to find a preconditioning phenomenon, whereby an initial depolarizing treatment leaves a residual pool of active PINK1 that remains competent to seed the activation of nascent cleaved PINK1 following a 16-hour recovery period.
Beschreibung:Gesehen am 25.07.2025
Beschreibung:Online Resource
ISSN:2375-2548
DOI:10.1126/sciadv.adr1938

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