Relationship Between METTL21C Gene Expression and Exercise in Human Skeletal Muscle: A Meta-Analysis
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PURPOSE: Recently, METTL21C has been identified as a potential pleiotropic gene for osteoporosis and sarcopenia. The purpose of this study was to collect gene expression datasets of human skeletal muscle transcriptome and to determine their relationship to exercise through meta-analysis. METHODS: MetaMEx was used to determine whether METTL21C in human skeletal muscle was associated with age, sex, physical activity and obesity. In addition, the difference in gene expression of METTL21C according to exercise duration and exercise type was confirmed. Using MetaMEx, top 300 genes (positive and negative, respectively) with a high correlation with METTL21C were selected, and gene ontology analysis was performed to identify related pathways. RESULTS:The expression of METTL21C gene in human skeletal muscle was significantly lower in the elderly than in young subjects (p<.0001), and significantly lower in female than in male (p<.0001). Also, the obese subjects were significantly lower than lean subjects (p<.0001). However, subjects with high level of physical activity had significantly higher expression of METTL21C than subjects with low levels of physical activity (p<.0001). Acute resistance exercise (p<.0001) and acute high-intensity interval training (p<.05) were found to have significantly higher expression of METTL21C in the skeletal muscle of the exercise group compared to the control group. Aerobic exercise training (p<.0001) and resistance exercise training (p<.0001) showed significantly higher expression of METTL21C in the skeletal muscle of the exercise group compared to the control group. CONCLUSIONS: Physical activity and exercise is important to prevent and treat osteosarcopenia because it can increase the expression of METTL21C in human skeletal muscle and maintain bone and muscle homeostasis.
Abstract
PURPOSE: Recently, METTL21C has been identified as a potential pleiotropic gene for osteoporosis and sarcopenia. The purpose of this study was to collect gene expression datasets of human skeletal muscle transcriptome and to determine their relationship to exercise through meta-analysis. METHODS: MetaMEx was used to determine whether METTL21C in human skeletal muscle was associated with age, sex, physical activity and obesity. In addition, the difference in gene expression of METTL21C according to exercise duration and exercise type was confirmed. Using MetaMEx, top 300 genes (positive and negative, respectively) with a high correlation with METTL21C were selected, and gene ontology analysis was performed to identify related pathways. RESULTS:The expression of METTL21C gene in human skeletal muscle was significantly lower in the elderly than in young subjects (p<.0001), and significantly lower in female than in male (p<.0001). Also, the obese subjects were significantly lower than lean subjects (p<.0001). However, subjects with high level of physical activity had significantly higher expression of METTL21C than subjects with low levels of physical activity (p<.0001). Acute resistance exercise (p<.0001) and acute high-intensity interval training (p<.05) were found to have significantly higher expression of METTL21C in the skeletal muscle of the exercise group compared to the control group. Aerobic exercise training (p<.0001) and resistance exercise training (p<.0001) showed significantly higher expression of METTL21C in the skeletal muscle of the exercise group compared to the control group. CONCLUSIONS: Physical activity and exercise is important to prevent and treat osteosarcopenia because it can increase the expression of METTL21C in human skeletal muscle and maintain bone and muscle homeostasis.
참고문헌 (30)
- Crepaldi G, "Sarcopenia and osteoporosis : a hazardous duet", J Endocrinol Invest, 28(10 Suppl), pp.66~68 (2005)
- Hiroshi Kaji, "Interaction between Muscle and Bone", 대한골대사학회지, 21(1), pp.29~40 (2014), 대한골대사학회
- Yu R, "Incremental predictive value of sarcopenia for incident fracture in an elderly chinese cohort : results from the osteoporotic fractures in men(MrOs)study", J Am Med Dir Assoc, 15(8), pp.551~558 (2014)
- Joseph C, "Role of endocrine-immune dysregulation in osteoporosis, sarcopenia, frailty and fracture risk", Mol Aspects Med, 26(3), pp.181~201 (2005)
- Sjoblom S, "Relationship between postmenopausal osteoporosis and the components of clinical sarcopenia", Maturitas, 75(2), pp.175~180 (2013)
- Sirola J, "Similarities in acquired factors related to postmenopausal osteoporosis and sarcopenia", J Osteoporos, 2011, pp.536735~ (2011)
- Kemp JP, "Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis", Nat Genet, 49(10), pp.1468~1475 (2017)
- Zillikens MC, "Large meta-analysis of genome-wide association studies identifies five loci for lean body mass", Nat Commun, 8(1), pp.80~ (2017)
- Willems SM, "Largescale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness", Nat Commun, 8, pp.16015~ (2017)
- Trajanoska K, "Genetics of bone and muscle interactions in humans", Curr Osteoporos Rep, 17(2), pp.86~95 (2019)
- Tikkanen E, "Biological insights into muscular strength : genetic findings in the UK biobank", Sci Rep, 8(1), pp.6451~ (2018)
- Guo YF, "Suggestion of GLYAT gene underlying variation of bone size and body lean mass as revealed by a bivariate genome-wide association study", Hum Genet, 132(2), pp.189~199 (2013)
- Gupta M, "Identification of homogeneous genetic architecture of multiple genetically correlated traits by block clustering of genome-wide associations", J Bone Miner Res, 26(6), pp.1261~1271 (2011)
- Kernstock S, "Lysine methylation of VCP by a member of a novel human protein methyltransferase family", Nat Commun, 3, pp.1038~ (2012)
- Kimonis VE, "VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia : review of a unique disorder", Biochim Biophys Acta, 1782(12), pp.744~748 (2008)
- Cloutier P, "A newly uncovered group of distantly related lysine methyltransferases preferentially interact with molecular chaperones to regulate their activity", PLoS Genet, 9(1), pp.e1003210~ (2013)
- Huang J, "METTL21C is a potential pleiotropic gene for osteoporosis and sarcopenia acting through the modulation of the NF-kappaB signaling pathway", J Bone Miner Res, 29(7), pp.1531~1540 (2014)
- Wiederstein JL, "Skeletal muscle-specific methyltransferase METTL21C Trimethylates p97 and regulates autophagy-associated protein breakdown", Cell Rep, 23(5), pp.1342~1356 (2018)
- Wang C, "Methyltransferase-like 21c methylates and stabilizes the heat shock protein Hspa8 in type I myofibers in mice", J Biol Chem, 294(37), pp.13718~13728 (2019)
- Chilibeck PD, "Exercise and bone mineral density", Sports Med, 19(2), pp.103~122 (1995)
- Suominen H, "Bone mineral density and long term exercise. An overview of cross-sectional athlete studies", Sports Med, 16(5), pp.316~330 (1993)
- Adamo ML, "Resistance training, and IGF involvement in the maintenance of muscle mass during the aging process", Ageing Res Rev, 5(3), pp.310~331 (2006)
- Pillon NJ, "Transcriptomic profiling of skeletal muscle adaptations to exercise and inactivity", Nat Commun, 11(1), pp.470~ (2020)
- Mi H, "Protocol Update for large-scale genome and gene function analysis with the PANTHER classification system (v.14.0)", Nat Protoc, 14(3), pp.703~721 (2019)
- Kim H, "Irisin mediates effects on bone and fat via alpha V integrin receptors", Cell, 178(2), pp.507~508 (2019)
- Rauch F, "Osteogenesis imperfecta", Lancet, 363(9418), pp.1377~1385 (2004)
- Gentry BA, "Skeletal muscle weakness in osteogenesis imperfecta mice", Matrix Biol, 29(7), pp.638~644 (2010)
- Watanabe S, "Serum C1q as a novel biomarker of sarcopenia in older adults", FASEB J, 29(3), pp.1003~1010 (2015)
- McMillan LB, "Prescribing Physical Activity for the prevention and treatment of osteoporosis in older adults", Healthcare. (Basel), 5(4) (2017)
- Nalbandian A, "Exercise training reverses skeletal muscle atrophy in an experimental model of VCP disease", PLoS One, 8(10), pp.e76187~ (2013)
