Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy.
Selenium is an essential trace element and selenoprotein N (SelN) was the first selenium-containing protein shown to be directly involved in human inherited diseases. Mutations in the SEPN1 gene, encoding SelN, cause a group of muscular disorders characterized by predominant affection of axial muscl...
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oai:doaj.org-article:be4eb237517f44e19d3891ab804ea5cd2021-11-18T06:48:28ZIncreased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy.1932-620310.1371/journal.pone.0023094https://doaj.org/article/be4eb237517f44e19d3891ab804ea5cd2011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21858002/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Selenium is an essential trace element and selenoprotein N (SelN) was the first selenium-containing protein shown to be directly involved in human inherited diseases. Mutations in the SEPN1 gene, encoding SelN, cause a group of muscular disorders characterized by predominant affection of axial muscles. SelN has been shown to participate in calcium and redox homeostasis, but its pathophysiological role in skeletal muscle remains largely unknown. To address SelN function in vivo, we generated a Sepn1-null mouse model by gene targeting. The Sepn1(-/-) mice had normal growth and lifespan, and were macroscopically indistinguishable from wild-type littermates. Only minor defects were observed in muscle morphology and contractile properties in SelN-deficient mice in basal conditions. However, when subjected to challenging physical exercise and stress conditions (forced swimming test), Sepn1(-/-) mice developed an obvious phenotype, characterized by limited motility and body rigidity during the swimming session, as well as a progressive curvature of the spine and predominant alteration of paravertebral muscles. This induced phenotype recapitulates the distribution of muscle involvement in patients with SEPN1-Related Myopathy, hence positioning this new animal model as a valuable tool to dissect the role of SelN in muscle function and to characterize the pathophysiological process.Mathieu RederstorffPerrine CastetsSandrine ArbogastJeanne LainéStéphane VassilopoulosMaud BeuvinOdile DubourgAlban VignaudArnaud FerryAlain KrolValérie AllamandPascale GuicheneyAna FerreiroAlain LescurePublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 8, p e23094 (2011) |
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Medicine R Science Q Mathieu Rederstorff Perrine Castets Sandrine Arbogast Jeanne Lainé Stéphane Vassilopoulos Maud Beuvin Odile Dubourg Alban Vignaud Arnaud Ferry Alain Krol Valérie Allamand Pascale Guicheney Ana Ferreiro Alain Lescure Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy. |
| description |
Selenium is an essential trace element and selenoprotein N (SelN) was the first selenium-containing protein shown to be directly involved in human inherited diseases. Mutations in the SEPN1 gene, encoding SelN, cause a group of muscular disorders characterized by predominant affection of axial muscles. SelN has been shown to participate in calcium and redox homeostasis, but its pathophysiological role in skeletal muscle remains largely unknown. To address SelN function in vivo, we generated a Sepn1-null mouse model by gene targeting. The Sepn1(-/-) mice had normal growth and lifespan, and were macroscopically indistinguishable from wild-type littermates. Only minor defects were observed in muscle morphology and contractile properties in SelN-deficient mice in basal conditions. However, when subjected to challenging physical exercise and stress conditions (forced swimming test), Sepn1(-/-) mice developed an obvious phenotype, characterized by limited motility and body rigidity during the swimming session, as well as a progressive curvature of the spine and predominant alteration of paravertebral muscles. This induced phenotype recapitulates the distribution of muscle involvement in patients with SEPN1-Related Myopathy, hence positioning this new animal model as a valuable tool to dissect the role of SelN in muscle function and to characterize the pathophysiological process. |
| format |
article |
| author |
Mathieu Rederstorff Perrine Castets Sandrine Arbogast Jeanne Lainé Stéphane Vassilopoulos Maud Beuvin Odile Dubourg Alban Vignaud Arnaud Ferry Alain Krol Valérie Allamand Pascale Guicheney Ana Ferreiro Alain Lescure |
| author_facet |
Mathieu Rederstorff Perrine Castets Sandrine Arbogast Jeanne Lainé Stéphane Vassilopoulos Maud Beuvin Odile Dubourg Alban Vignaud Arnaud Ferry Alain Krol Valérie Allamand Pascale Guicheney Ana Ferreiro Alain Lescure |
| author_sort |
Mathieu Rederstorff |
| title |
Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy. |
| title_short |
Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy. |
| title_full |
Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy. |
| title_fullStr |
Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy. |
| title_full_unstemmed |
Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy. |
| title_sort |
increased muscle stress-sensitivity induced by selenoprotein n inactivation in mouse: a mammalian model for sepn1-related myopathy. |
| publisher |
Public Library of Science (PLoS) |
| publishDate |
2011 |
| url |
https://doaj.org/article/be4eb237517f44e19d3891ab804ea5cd |
| work_keys_str_mv |
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