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      α-Syntrophin Modulates Myogenin Expression in Differentiating Myoblasts

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          Abstract

          Background

          α-Syntrophin is a scaffolding protein linking signaling proteins to the sarcolemmal dystrophin complex in mature muscle. However, α-syntrophin is also expressed in differentiating myoblasts during the early stages of muscle differentiation. In this study, we examined the relationship between the expression of α-syntrophin and myogenin, a key muscle regulatory factor.

          Methods and Findings

          The absence of α-syntrophin leads to reduced and delayed myogenin expression. This conclusion is based on experiments using muscle cells isolated from α-syntrophin null mice, muscle regeneration studies in α-syntrophin null mice, experiments in Sol8 cells (a cell line that expresses only low levels of α-syntrophin) and siRNA studies in differentiating C2 cells. In primary cultured myocytes isolated from α-syntrophin null mice, the level of myogenin was less than 50% that from wild type myocytes ( p<0.005) 40 h after differentiation induction. In regenerating muscle, the expression of myogenin in the α-syntrophin null muscle was reduced to approximately 25% that of wild type muscle ( p<0.005). Conversely, myogenin expression is enhanced in primary cultures of myoblasts isolated from a transgenic mouse over-expressing α-syntrophin and in Sol8 cells transfected with a vector to over-express α-syntrophin. Moreover, we find that myogenin mRNA is reduced in the absence of α-syntrophin and increased by α-syntrophin over-expression. Immunofluorescence microscopy shows that α-syntrophin is localized to the nuclei of differentiating myoblasts. Finally, immunoprecipitation experiments demonstrate that α-syntrophin associates with Mixed-Lineage Leukemia 5, a regulator of myogenin expression.

          Conclusions

          We conclude that α-syntrophin plays an important role in regulating myogenesis by modulating myogenin expression.

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          Most cited references37

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          Genome regulation by polycomb and trithorax proteins.

          Polycomb group (PcG) and trithorax group (trxG) proteins are critical regulators of numerous developmental genes. To silence or activate gene expression, respectively, PcG and trxG proteins bind to specific regions of DNA and direct the posttranslational modification of histones. Recent work suggests that PcG proteins regulate the nuclear organization of their target genes and that PcG-mediated gene silencing involves noncoding RNAs and the RNAi machinery.
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            Myogenic satellite cells: physiology to molecular biology.

            Adult skeletal muscle has a remarkable ability to regenerate following myotrauma. Because adult myofibers are terminally differentiated, the regeneration of skeletal muscle is largely dependent on a small population of resident cells termed satellite cells. Although this population of cells was identified 40 years ago, little is known regarding the molecular phenotype or regulation of the satellite cell. The use of cell culture techniques and transgenic animal models has improved our understanding of this unique cell population; however, the capacity and potential of these cells remain ill-defined. This review will highlight the origin and unique markers of the satellite cell population, the regulation by growth factors, and the response to physiological and pathological stimuli. We conclude by highlighting the potential therapeutic uses of satellite cells and identifying future research goals for the study of satellite cell biology.
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              • Record: found
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              Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle.

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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2010
                17 December 2010
                : 5
                : 12
                : e15355
                Affiliations
                [1 ]Department of Biological Science, Ajou University, Suwon, Korea
                [2 ]Department of Physiology & Biophysics, University of Washington, Seattle, Washington, United States of America
                McMaster University, Canada
                Author notes

                Conceived and designed the experiments: MK SCF HK MEA. Performed the experiments: MK SH JL MEA HK. Analyzed the data: MK SH JL SCF MEA HK. Contributed reagents/materials/analysis tools: SCF MEA HK. Wrote the paper: MK SCF MEA HK.

                Article
                PONE-D-10-01357
                10.1371/journal.pone.0015355
                3003685
                21179410
                86ad6a7f-9b39-4597-839b-e9972c1a80d8
                Kim et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 26 August 2010
                : 11 November 2010
                Page count
                Pages: 10
                Categories
                Research Article
                Biology
                Anatomy and Physiology
                Musculoskeletal System
                Muscle
                Muscle Biochemistry
                Cell Physiology
                Developmental Biology
                Molecular Development
                Signaling
                Cell Differentiation
                Cell Fate Determination
                Model Organisms
                Animal Models
                Mouse
                Medicine
                Anatomy and Physiology
                Musculoskeletal System
                Muscle
                Muscle Biochemistry

                Uncategorized
                Uncategorized

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