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Transcriptomic Analysis of Single Isolated Myofibers Identifies miR-27a-3p and miR-142-3p as Regulators of Metabolism in Skeletal Muscle

Authors :
Francesco Chemello
Francesca Grespi
Alessandra Zulian
Pasqua Cancellara
Etienne Hebert-Chatelain
Paolo Martini
Camilla Bean
Enrico Alessio
Lisa Buson
Martina Bazzega
Andrea Armani
Marco Sandri
Ruggero Ferrazza
Paolo Laveder
Graziano Guella
Carlo Reggiani
Chiara Romualdi
Paolo Bernardi
Luca Scorrano
Stefano Cagnin
Gerolamo Lanfranchi
Source :
Cell Reports, Vol 26, Iss 13, Pp 3784-3797.e8 (2019)
Publication Year :
2019
Publisher :
Elsevier, 2019.

Abstract

Summary: Skeletal muscle is composed of different myofiber types that preferentially use glucose or lipids for ATP production. How fuel preference is regulated in these post-mitotic cells is largely unknown, making this issue a key question in the fields of muscle and whole-body metabolism. Here, we show that microRNAs (miRNAs) play a role in defining myofiber metabolic profiles. mRNA and miRNA signatures of all myofiber types obtained at the single-cell level unveiled fiber-specific regulatory networks and identified two master miRNAs that coordinately control myofiber fuel preference and mitochondrial morphology. Our work provides a complete and integrated mouse myofiber type-specific catalog of gene and miRNA expression and establishes miR-27a-3p and miR-142-3p as regulators of lipid use in skeletal muscle. : Chemello et al. characterize coding mRNAs and non-coding microRNAs expressed by myofibers of hindlimb mouse muscles, identifying complex interactions between these molecules that modulate mitochondrial functions and muscle metabolism. They demonstrate that specific short non-coding RNAs influence the contractile fiber composition of skeletal muscles by modulating muscle metabolism. Keywords: single myofiber, skeletal muscle metabolism, mitochondria, miRNAs, lipids

Subjects

Subjects :
Biology (General)
QH301-705.5

Details

Language :
English
ISSN :
22111247
Volume :
26
Issue :
13
Database :
Directory of Open Access Journals
Journal :
Cell Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.f1aadd031b6e4843b189ce5480836280
Document Type :
article
Full Text :
https://doi.org/10.1016/j.celrep.2019.02.105