| Literature DB >> 35216662 |
Angelika B Harbauer1, J Tabitha Hees2, Simone Wanderoy2, Inmaculada Segura3, Whitney Gibbs4, Yiming Cheng5, Martha Ordonez4, Zerong Cai4, Romain Cartoni6, Ghazaleh Ashrafi4, Chen Wang6, Fabiana Perocchi7, Zhigang He6, Thomas L Schwarz8.
Abstract
PTEN-induced kinase 1 (PINK1) is a short-lived protein required for the removal of damaged mitochondria through Parkin translocation and mitophagy. Because the short half-life of PINK1 limits its ability to be trafficked into neurites, local translation is required for this mitophagy pathway to be active far from the soma. The Pink1 transcript is associated and cotransported with neuronal mitochondria. In concert with translation, the mitochondrial outer membrane proteins synaptojanin 2 binding protein (SYNJ2BP) and synaptojanin 2 (SYNJ2) are required for tethering Pink1 mRNA to mitochondria via an RNA-binding domain in SYNJ2. This neuron-specific adaptation for the local translation of PINK1 provides distal mitochondria with a continuous supply of PINK1 for the activation of mitophagy.Entities:
Keywords: OMP25; PINK1; Parkinson disease; RNA transport; SYNJ2BP; hitchhiking; local translation; mitophagy; synaptojanin2
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Year: 2022 PMID: 35216662 PMCID: PMC9081165 DOI: 10.1016/j.neuron.2022.01.035
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 18.688