Late Endosomes Act as mRNA Translation Platforms and Sustain Mitochondria in Axons

Jean-Michel Cioni, Julie Qiaojin Lin, Anne V. Holtermann, Max Koppers, Maximilian A.H. Jakobs, Afnan Azizi, Benita Turner-Bridger, Toshiaki Shigeoka, Kristian Franze, William A. Harris, Christine E. Holt

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

© 2018 The AuthorsLocal translation regulates the axonal proteome, playing an important role in neuronal wiring and axon maintenance. How axonal mRNAs are localized to specific subcellular sites for translation, however, is not understood. Here we report that RNA granules associate with endosomes along the axons of retinal ganglion cells. RNA-bearing Rab7a late endosomes also associate with ribosomes, and real-time translation imaging reveals that they are sites of local protein synthesis. We show that RNA-bearing late endosomes often pause on mitochondria and that mRNAs encoding proteins for mitochondrial function are translated on Rab7a endosomes. Disruption of Rab7a function with Rab7a mutants, including those associated with Charcot-Marie-Tooth type 2B neuropathy, markedly decreases axonal protein synthesis, impairs mitochondrial function, and compromises axonal viability. Our findings thus reveal that late endosomes interact with RNA granules, translation machinery, and mitochondria and suggest that they serve as sites for regulating the supply of nascent pro-survival proteins in axons. © 2018 The AuthorsLate endosomes are sites of local translation of mRNAs important for mitochondrial maintenance, and perturbing this process can contribute to neuropathology, as seen in Charcot Marie-Tooth disease.
Original languageEnglish
Pages (from-to)56-72.e15
JournalCell
Volume176
Issue number1-2
DOIs
Publication statusPublished - 10 Jan 2019
Externally publishedYes

Funding

We thank Nicola Lawrence, Katrin Mooslehner, and Asha Dwivedy for technical assistance and Matthew Seaman for valuable discussions. This work was supported by an EMBO long-term fellowship (to J.-M.C.); a Gates Cambridge scholarship (to J.Q.L.); the German Academic Exchange Program (DAAD) and a German National Academic Foundation scholarship (to A.V.H.); the Cambridge Wellcome Trust PhD Programme in Developmental Biology (to M.A.H.J., A.A., and B.T.-B.); the Cambridge Commonwealth , European and International Trust , and Natural Sciences and Engineering Research Council of Canada (to A.A.); the Netherlands Organization for Scientific Research ( NWO Rubicon ) (to M.K.); BBSRC Research Grant BB/N006402/1 (to K.F.); Wellcome Trust Investigator Award ( SIA 100329/Z/12/Z ) (to W.A.H.); and Wellcome Trust grants ( 085314/Z/08/Z and 203249/Z/16/Z ) and European Research Council advanced grant ( 322817 ) (to C.E.H.).

FundersFunder number
Netherlands Organization for Scientific Research
Wellcome TrustSIA 100329/Z/12/Z, 085314/Z/08/Z, 203249/Z/16/Z
Seventh Framework Programme322817
Natural Sciences and Engineering Research Council of Canada
Biotechnology and Biological Sciences Research CouncilBB/N006402/1
European Research Council
German Academic Exchange Service London
Deutscher Akademischer Austauschdienst
EMBO
Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Studienstiftung des Deutschen Volkes
Gates Cambridge Trust

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