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Identification of 3' UTR motifs required for mRNA localization to myelin sheaths in vivo.

Authors :
Yergert KM
Doll CA
O'Rouke R
Hines JH
Appel B
Source :
PLoS biology [PLoS Biol] 2021 Jan 13; Vol. 19 (1), pp. e3001053. Date of Electronic Publication: 2021 Jan 13 (Print Publication: 2021).
Publication Year :
2021

Abstract

Myelin is a specialized membrane produced by oligodendrocytes that insulates and supports axons. Oligodendrocytes extend numerous cellular processes, as projections of the plasma membrane, and simultaneously wrap multiple layers of myelin membrane around target axons. Notably, myelin sheaths originating from the same oligodendrocyte are variable in size, suggesting local mechanisms regulate myelin sheath growth. Purified myelin contains ribosomes and hundreds of mRNAs, supporting a model that mRNA localization and local protein synthesis regulate sheath growth and maturation. However, the mechanisms by which mRNAs are selectively enriched in myelin sheaths are unclear. To investigate how mRNAs are targeted to myelin sheaths, we tested the hypothesis that transcripts are selected for myelin enrichment through consensus sequences in the 3' untranslated region (3' UTR). Using methods to visualize mRNA in living zebrafish larvae, we identified candidate 3' UTRs that were sufficient to localize mRNA to sheaths and enriched near growth zones of nascent membrane. We bioinformatically identified motifs common in 3' UTRs from 3 myelin-enriched transcripts and determined that these motifs are required and sufficient in a context-dependent manner for mRNA transport to myelin sheaths. Finally, we show that 1 motif is highly enriched in the myelin transcriptome, suggesting that this sequence is a global regulator of mRNA localization during developmental myelination.<br />Competing Interests: The authors have declared that no competing interests exist.

Details

Language :
English
ISSN :
1545-7885
Volume :
19
Issue :
1
Database :
MEDLINE
Journal :
PLoS biology
Publication Type :
Academic Journal
Accession number :
33439856
Full Text :
https://doi.org/10.1371/journal.pbio.3001053