The translatome of neuronal cell bodies, dendrites, and axons.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
26 10 2021
Historique:
accepted: 08 09 2021
entrez: 21 10 2021
pubmed: 22 10 2021
medline: 31 12 2021
Statut: ppublish

Résumé

To form synaptic connections and store information, neurons continuously remodel their proteomes. The impressive length of dendrites and axons imposes logistical challenges to maintain synaptic proteins at locations remote from the transcription source (the nucleus). The discovery of thousands of messenger RNAs (mRNAs) near synapses suggested that neurons overcome distance and gain autonomy by producing proteins locally. It is not generally known, however, if, how, and when localized mRNAs are translated into protein. To investigate the translational landscape in neuronal subregions, we performed simultaneous RNA sequencing (RNA-seq) and ribosome sequencing (Ribo-seq) from microdissected rodent brain slices to identify and quantify the transcriptome and translatome in cell bodies (somata) as well as dendrites and axons (neuropil). Thousands of transcripts were differentially translated between somatic and synaptic regions, with many scaffold and signaling molecules displaying increased translation levels in the neuropil. Most translational changes between compartments could be accounted for by differences in RNA abundance. Pervasive translational regulation was observed in both somata and neuropil influenced by specific mRNA features (e.g., untranslated region [UTR] length, RNA-binding protein [RBP] motifs, and upstream open reading frames [uORFs]). For over 800 mRNAs, the dominant source of translation was the neuropil. We constructed a searchable and interactive database for exploring mRNA transcripts and their translation levels in the somata and neuropil [MPI Brain Research, The mRNA translation landscape in the synaptic neuropil. https://public.brain.mpg.de/dashapps/localseq/ Accessed 5 October 2021]. Overall, our findings emphasize the substantial contribution of local translation to maintaining synaptic protein levels and indicate that on-site translational control is an important mechanism to control synaptic strength.

Identifiants

pubmed: 34670838
pii: 2113929118
doi: 10.1073/pnas.2113929118
pmc: PMC8639352
pii:
doi:

Substances chimiques

Proteome 0
RNA, Messenger 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 the Author(s). Published by PNAS.

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

Caspar Glock (C)

Department of Synaptic Plasticity, Max Planck Institut fur Hirnforschung, Frankfurt am Main, Hessen 60438, Germany.

Anne Biever (A)

Department of Synaptic Plasticity, Max Planck Institut fur Hirnforschung, Frankfurt am Main, Hessen 60438, Germany.

Georgi Tushev (G)

Department of Synaptic Plasticity, Max Planck Institut fur Hirnforschung, Frankfurt am Main, Hessen 60438, Germany.

Belquis Nassim-Assir (B)

Department of Synaptic Plasticity, Max Planck Institut fur Hirnforschung, Frankfurt am Main, Hessen 60438, Germany.

Allison Kao (A)

Department of Synaptic Plasticity, Max Planck Institut fur Hirnforschung, Frankfurt am Main, Hessen 60438, Germany.

Ina Bartnik (I)

Department of Synaptic Plasticity, Max Planck Institut fur Hirnforschung, Frankfurt am Main, Hessen 60438, Germany.

Susanne Tom Dieck (S)

Department of Synaptic Plasticity, Max Planck Institut fur Hirnforschung, Frankfurt am Main, Hessen 60438, Germany.

Erin M Schuman (EM)

Department of Synaptic Plasticity, Max Planck Institut fur Hirnforschung, Frankfurt am Main, Hessen 60438, Germany erin.schuman@brain.mpg.de.

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