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Updated: Jun 11, 2025

Skeletal Muscle Gender Dimorphism from Proteomics
Published on: December 14, 2011
Molecular composition of skeletal muscle in infants and adults: a comparative proteomic and transcriptomic study
Alexander Schaiter1, Andreas Hentschel2, Felix Kleefeld3,4
1Institute of Neuropathology, Justus-Liebig University, Giessen, Germany.
Insights
This study reveals molecular differences in infant versus adult skeletal muscle, showing that aging processes begin earlier than previously thought. Understanding these molecular signatures is key for healthy muscle development and aging research.
Area of Science:
- Molecular Biology
- Physiology
- Gerontology
Background:
- Skeletal muscle function is crucial throughout life, yet molecular data comparing infant and adult muscle is scarce.
- Understanding age-related molecular changes is vital for comprehending muscle development and aging.
- Existing research often overlooks infant muscle, creating a knowledge gap in developmental muscle biology.
Purpose of the Study:
- To investigate molecular signatures in infant and adult skeletal muscle.
- To compare morphological, transcriptomic, and proteomic profiles across age groups.
- To identify age-related differences in healthy skeletal muscle function.
Main Methods:
- RNA sequencing (RNA-seq) for gene expression analysis.
- Tandem mass spectrometry (LC-MS/MS) for protein profiling.
- Morphometric analysis and mitochondrial maintenance assays on muscle biopsies.
Main Results:
- Identified differentially expressed genes (DEGs) and proteins (DEPs) between infants and adults.
- Down-regulated genes in adults were linked to sarcomeres, cellular maintenance, metabolism, immunity, and development.
- Revealed age-related molecular signatures impacting skeletal muscle function.
Conclusions:
- Significant age-related molecular differences exist in healthy skeletal muscle.
- Processes once attributed solely to aging are present during development and healthy aging.
- Age-specific controls are essential for reliable muscle disease research.
Abstract:
To gain a deeper understanding of skeletal muscle function in younger age and aging in elderly, identification of molecular signatures regulating these functions under physiological conditions is needed. Although molecular studies of healthy muscle have been conducted on adults and older subjects, there is a lack of research on infant muscle in terms of combined morphological, transcriptomic and proteomic profiles. To address this gap of knowledge, we performed RNA sequencing (RNA-seq), tandem mass spectrometry (LC-MS/MS), morphometric analysis and assays for mitochondrial maintenance in skeletal muscle biopsies from both, infants aged 4-28 months and adults aged 19-65 years. We identified differently expressed genes (DEGs) and differentially expressed proteins (DEPs) in adults compared to infants. The down-regulated genes in adults were associated with functional terms primarily related to sarcomeres, cellular maintenance, and metabolic, immunological and developmental processes. Thus, our study indicates age-related differences in the molecular signatures and associated functions of healthy skeletal muscle. Moreover, the findings assert that processes previously associated solely with aging are indeed part of development and healthy aging. Hence, combined findings of this study also indicate that age-dependent controls are crucial in muscle disease studies, as otherwise the comparative results may not be reliable.
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