Locally translated mTOR controls axonal local translation in nerve injury

Author:

Terenzio Marco1ORCID,Koley Sandip1,Samra Nitzan1ORCID,Rishal Ida1ORCID,Zhao Qian2ORCID,Sahoo Pabitra K.3,Urisman Anatoly2ORCID,Marvaldi Letizia1,Oses-Prieto Juan A.2ORCID,Forester Craig4ORCID,Gomes Cynthia3ORCID,Kalinski Ashley L.3ORCID,Di Pizio Agostina1,Doron-Mandel Ella1ORCID,Perry Rotem Ben-Tov1,Koppel Indrek1,Twiss Jeffery L.35ORCID,Burlingame Alma L.2,Fainzilber Mike1ORCID

Affiliation:

1. Department of Biomolecular Sciences, Weizmann Institute of Science, Rehovot 76100, Israel.

2. Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94158, USA.

3. Department of Biological Sciences, University of South Carolina, Columbia, SC 29208, USA.

4. Division of Pediatric Allergy, Immunology and Bone Marrow Transplantation, University of California, San Francisco, CA 94158, USA.

5. Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA 19129, USA.

Abstract

Local control of localized protein synthesis Localized protein synthesis provides spatiotemporal precision for injury responses and growth decisions at remote positions in nerve axons. Terenzio et al. show that this process is controlled by local translation of preexisting axonal mRNA encoding the master regulator mTOR (see the Perspective by Riccio). mTOR controls both its own synthesis and that of most newly synthesized proteins at axonal injury sites, thereby determining the subsequent survival and growth of the injured neuron. Science , this issue p. 1416 ; see also p. 1331

Funder

National Institutes of Health

Congressionally Directed Medical Research Programs

Dr. Miriam and Sheldon G. Adelson Medical Research Foundation

European Research Council

Minerva Foundation

Israel Science Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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