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MicroRNA sequence codes for small extracellular vesicle release and cellular retention.

Citation
Garcia-Martin, R., et al. “Microrna Sequence Codes For Small Extracellular Vesicle Release And Cellular Retention.”. Nature, pp. 446-451.
Center Joslin Diabetes Center
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Author Ruben Garcia-Martin, GuoXiao Wang, Bruna B Brandão, Tamires M Zanotto, Samah Shah, Sandip Kumar Patel, Birgit Schilling, Ronald Kahn
Abstract

Exosomes and other small extracellular vesicles (sEVs) provide a unique mode of cell-to-cell communication in which microRNAs (miRNAs) produced and released from one cell are taken up by cells at a distance where they can enact changes in gene expression. However, the mechanism by which miRNAs are sorted into exosomes/sEVs or retained in cells remains largely unknown. Here we demonstrate that miRNAs possess sorting sequences that determine their secretion in sEVs (EXOmotifs) or cellular retention (CELLmotifs) and that different cell types, including white and brown adipocytes, endothelium, liver and muscle, make preferential use of specific sorting sequences, thus defining the sEV miRNA profile of that cell type. Insertion or deletion of these CELLmotifs or EXOmotifs in a miRNA increases or decreases retention in the cell of production or secretion into exosomes/sEVs. Two RNA-binding proteins, Alyref and Fus, are involved in the export of miRNAs carrying one of the strongest EXOmotifs, CGGGAG. Increased miRNA delivery mediated by EXOmotifs leads to enhanced inhibition of target genes in distant cells. Thus, this miRNA code not only provides important insights that link circulating exosomal miRNAs to tissues of origin, but also provides an approach for improved targeting in RNA-mediated therapies.

Year of Publication
2022
Journal
Nature
Volume
601
Issue
7893
Number of Pages
446-451
Date Published
01/2022
ISSN Number
1476-4687
DOI
10.1038/s41586-021-04234-3
Alternate Journal
Nature
PMID
34937935
PMCID
PMC9035265
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