The myonuclear domain in adult skeletal muscle fibres: past, present and future

Author:

Bagley James R.1ORCID,Denes Lance T.2ORCID,McCarthy John J.34ORCID,Wang Eric T.567ORCID,Murach Kevin A.89ORCID

Affiliation:

1. Muscle Physiology Laboratory, Department of Kinesiology San Francisco State University San Francisco CA USA

2. Institute for Systems Genetics New York University New York NY USA

3. The Center for Muscle Biology University of Kentucky Lexington KY USA

4. Department of Physiology, College of Medicine University of Kentucky Lexington KY USA

5. Department of Molecular Genetics and Microbiology, Center for NeuroGenetics University of Florida Gainesville FL USA

6. Myology Institute University of Florida Gainesville FL USA

7. Genetics Institute University of Florida Gainesville FL USA

8. Exercise Science Research Center, Department of Health, Human Performance, and Recreation University of Arkansas Fayetteville Arkansas USA

9. Cell and Molecular Biology Graduate Program University of Arkansas Fayetteville AR USA

Abstract

AbstractMost cells in the body are mononuclear whereas skeletal muscle fibres are uniquely multinuclear. The nuclei of muscle fibres (myonuclei) are usually situated peripherally which complicates the equitable distribution of gene products. Myonuclear abundance can also change under conditions such as hypertrophy and atrophy. Specialised zones in muscle fibres have different functions and thus distinct synthetic demands from myonuclei. The complex structure and regulatory requirements of multinuclear muscle cells understandably led to the hypothesis that myonuclei govern defined ‘domains’ to maintain homeostasis and facilitate adaptation. The purpose of this review is to provide historical context for the myonuclear domain and evaluate its veracity with respect to mRNA and protein distribution resulting from myonuclear transcription. We synthesise insights from past and current in vitro and in vivo genetically modified models for studying the myonuclear domain under dynamic conditions. We also cover the most contemporary knowledge on mRNA and protein transport in muscle cells. Insights from emerging technologies such as single myonuclear RNA‐sequencing further inform our discussion of the myonuclear domain. We broadly conclude: (1) the myonuclear domain can be flexible during muscle fibre growth and atrophy, (2) the mechanisms and role of myonuclear loss and motility deserve further consideration, (3) mRNA in muscle is actively transported via microtubules and locally restricted, but proteins may travel far from a myonucleus of origin and (4) myonuclear transcriptional specialisation extends beyond the classic neuromuscular and myotendinous populations. A deeper understanding of the myonuclear domain in muscle may promote effective therapies for ageing and disease. image

Funder

NIH Clinical Center

Publisher

Wiley

Subject

Physiology

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