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      PPARGC1A rs8192678 and NRF1 rs6949152 Polymorphisms Are Associated with Muscle Fiber Composition in Women

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          Abstract

          PPARGC1A rs8192678 G/A (Gly482Ser) and NRF1 rs6949152 A/G polymorphisms have been associated with endurance athlete status, endurance performance phenotypes, and certain health-related markers of different pathologies such as metabolic syndrome, diabetes, and dyslipidemia. We hypothesized that they could be considered interesting candidates for explaining inter-individual variations in muscle fiber composition in humans. We aimed to examine possible associations of these polymorphisms with myosin heavy-chain (MHC) isoforms as markers of muscle fiber compositions in vastus lateralis muscle in a population of 214 healthy Japanese subjects, aged between 19 and 79 years. No significant associations were found in men for any measured variables. In contrast, in women, the PPARGC1A rs8192678 A/A genotype was significantly associated with a higher proportion of MHC-I ( p = 0.042) and with a lower proportion of MHC-IIx ( p = 0.033), and the NRF1 rs6949152 AA genotype was significantly associated with a higher proportion of MHC-I ( p = 0.008) and with a lower proportion of MHC IIx ( p = 0.035). In women, the genotype scores of the modes presenting the most significant results for PPARGC1A rs8192678 G/A (Gly482Ser) and NRF1 rs6949152 A/G polymorphisms were significantly associated with MHC-I ( p = 0.0007) and MHC IIx ( p = 0.0016). That is, women with combined PPARGC1A A/A and NRF1 A/A genotypes presented the highest proportion of MHC-I and the lowest proportion of MHC-IIx, in contrast to women with combined PPARGC1A GG+GA and NRF1 AG+GG genotypes, who presented the lowest proportion of MHC-I and the highest proportion of MHC-IIx. Our results suggest possible associations between these polymorphisms (both individually and in combination) and the inter-individual variability observed in muscle fiber composition in women, but not in men.

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          Most cited references57

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          Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1.

          Mitochondrial number and function are altered in response to external stimuli in eukaryotes. While several transcription/replication factors directly regulate mitochondrial genes, the coordination of these factors into a program responsive to the environment is not understood. We show here that PGC-1, a cold-inducible coactivator of nuclear receptors, stimulates mitochondrial biogenesis and respiration in muscle cells through an induction of uncoupling protein 2 (UCP-2) and through regulation of the nuclear respiratory factors (NRFs). PGC-1 stimulates a powerful induction of NRF-1 and NRF-2 gene expression; in addition, PGC-1 binds to and coactivates the transcriptional function of NRF-1 on the promoter for mitochondrial transcription factor A (mtTFA), a direct regulator of mitochondrial DNA replication/transcription. These data elucidate a pathway that directly links external physiological stimuli to the regulation of mitochondrial biogenesis and function.
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            Transcriptional co-activator PGC-1 alpha drives the formation of slow-twitch muscle fibres.

            The biochemical basis for the regulation of fibre-type determination in skeletal muscle is not well understood. In addition to the expression of particular myofibrillar proteins, type I (slow-twitch) fibres are much higher in mitochondrial content and are more dependent on oxidative metabolism than type II (fast-twitch) fibres. We have previously identified a transcriptional co-activator, peroxisome-proliferator-activated receptor-gamma co-activator-1 (PGC-1 alpha), which is expressed in several tissues including brown fat and skeletal muscle, and that activates mitochondrial biogenesis and oxidative metabolism. We show here that PGC-1 alpha is expressed preferentially in muscle enriched in type I fibres. When PGC-1 alpha is expressed at physiological levels in transgenic mice driven by a muscle creatine kinase (MCK) promoter, a fibre type conversion is observed: muscles normally rich in type II fibres are redder and activate genes of mitochondrial oxidative metabolism. Notably, putative type II muscles from PGC-1 alpha transgenic mice also express proteins characteristic of type I fibres, such as troponin I (slow) and myoglobin, and show a much greater resistance to electrically stimulated fatigue. Using fibre-type-specific promoters, we show in cultured muscle cells that PGC-1 alpha activates transcription in cooperation with Mef2 proteins and serves as a target for calcineurin signalling, which has been implicated in slow fibre gene expression. These data indicate that PGC-1 alpha is a principal factor regulating muscle fibre type determination.
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              Skeletal muscle fiber-type switching, exercise intolerance, and myopathy in PGC-1alpha muscle-specific knock-out animals.

              The transcriptional coactivator peroxisome proliferator-activated receptor gamma coactivator 1alpha (PGC-1alpha) is a key integrator of neuromuscular activity in skeletal muscle. Ectopic expression of PGC-1alpha in muscle results in increased mitochondrial number and function as well as an increase in oxidative, fatigue-resistant muscle fibers. Whole body PGC-1alpha knock-out mice have a very complex phenotype but do not have a marked skeletal muscle phenotype. We thus analyzed skeletal muscle-specific PGC-1alpha knock-out mice to identify a specific role for PGC-1alpha in skeletal muscle function. These mice exhibit a shift from oxidative type I and IIa toward type IIx and IIb muscle fibers. Moreover, skeletal muscle-specific PGC-1alpha knock-out animals have reduced endurance capacity and exhibit fiber damage and elevated markers of inflammation following treadmill running. Our data demonstrate a critical role for PGC-1alpha in maintenance of normal fiber type composition and of muscle fiber integrity following exertion.
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                Author and article information

                Journal
                Genes (Basel)
                Genes (Basel)
                genes
                Genes
                MDPI
                2073-4425
                27 August 2020
                September 2020
                : 11
                : 9
                : 1012
                Affiliations
                [1 ]Graduate School of Health and Sports Science, Juntendo University, Chiba 270-1695, Japan; thomaspaul.yvert@ 123456universidadeuropea.es (T.Y.); eri-miyamoto@ 123456juntendo.ac.jp (E.M.-M.); mizuki854@ 123456gmail.com (M.T.); noriko.sekine@ 123456ouj.ac.jp (N.I.-S.); hnaitou@ 123456juntendo.ac.jp (H.N.)
                [2 ]Faculty of Sport Sciences, Universidad Europea de Madrid, 28670 Madrid, Spain; margarita.perez@ 123456universidadeuropea.es
                [3 ]Faculty of Nursing and Nutrition, University of Nagasaki, Nagasaki 851-2195, Japan; tobitaku@ 123456sun.ac.jp
                [4 ]Faculty of Education, University of Miyazaki, Miyazaki 889-2192, Japan; kshiose@ 123456cc.miyazaki-u.ac.jp
                [5 ]Faculty of Management & Information Science, Josai International University, Chiba 283-8555, Japan; rkakigi@ 123456jiu.ac.jp
                [6 ]Faculty of Pharmacy, Meijo University, Aichi 468-8503, Japan; takamasa425@ 123456gmail.com
                [7 ]Faculty of Liberal Arts, The Open University of Japan, Chiba 261-8586, Japan
                [8 ]Department of General Medicine, Mito Medical Center, Tsukuba University Hospital, Ibaraki 310-0015, Japan; hrkoba1@ 123456gmail.com
                [9 ]Faculty of Sports and Health Science, Fukuoka University, Fukuoka 814-0180, Japan
                Author notes
                [* ]Correspondence: noriyuki.fuku@ 123456nifty.com ; Tel.: +81-476-98-1001 (ext. 9203)
                [†]

                Deceased 23 April 2018.

                Author information
                https://orcid.org/0000-0002-9451-9799
                https://orcid.org/0000-0003-4789-2563
                https://orcid.org/0000-0003-1089-9593
                https://orcid.org/0000-0002-0467-3312
                https://orcid.org/0000-0002-0522-9512
                https://orcid.org/0000-0001-7792-5835
                Article
                genes-11-01012
                10.3390/genes11091012
                7563119
                32867330
                ae8ebaab-5eb6-4966-8665-2e20e418861c
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 29 July 2020
                : 25 August 2020
                Categories
                Article

                snp,myosin heavy chain,pgc-1α,nuclear respiratory factor,genotype score

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