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On-Site Ribosome Remodeling by Locally Synthesized Ribosomal Proteins in Axons
Author(s) -
Toshiaki Shigeoka,
Max Koppers,
Hovy HoWai Wong,
Julie Qiaojin Lin,
Roberta Cagnetta,
Asha Dwivedy,
Janaina De Freitas Nascimento,
Francesca W. van Tartwijk,
Florian Ströhl,
Jean-Michel Cioni,
Julia Schaeffer,
Mark Carrington,
Clemens F. Kaminski,
Hosung Jung,
William A. Harris,
Christine E. Holt
Publication year - 2019
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2019.11.025
Subject(s) - translation (biology) , nucleolus , ribosome , biology , ribosome profiling , ribosomal rna , microbiology and biotechnology , axon , ribosomal protein , internal ribosome entry site , protein biosynthesis , rna , cytoplasm , messenger rna , genetics , gene
Ribosome assembly occurs mainly in the nucleolus, yet recent studies have revealed robust enrichment and translation of mRNAs encoding many ribosomal proteins (RPs) in axons, far away from neuronal cell bodies. Here, we report a physical and functional interaction between locally synthesized RPs and ribosomes in the axon. We show that axonal RP translation is regulated through a sequence motif, CUIC, that forms an RNA-loop structure in the region immediately upstream of the initiation codon. Using imaging and subcellular proteomics techniques, we show that RPs synthesized in axons join axonal ribosomes in a nucleolus-independent fashion. Inhibition of axonal CUIC-regulated RP translation decreases local translation activity and reduces axon branching in the developing brain, revealing the physiological relevance of axonal RP synthesis in vivo. These results suggest that axonal translation supplies cytoplasmic RPs to maintain/modify local ribosomal function far from the nucleolus in neurons.

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