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Título: | Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy |
Autor: | Estañ, María Cristina CSIC; Fernández-Núñez, Elisa CSIC; Zaki, Maha S.; Esteban Rodriguez, Isabel; Donkervoort, Sandra; Hawkins, Cynthia; Caparrós-Martín, José A. CSIC; Saade, Dimah; Hu, Ying; Bolduc, Véronique; Ru-Yui Chao, Katherine; Nevado, Julian; Lamuedra, Ana; Largo, Raquel; Herrero-Beaumont, Gabriel; Regadera, Javier; Hernández-Chico, Concepción; Tizzano, Eduardo F.; Martinez-Glez, Víctor; Carvajal, Jaime J. CSIC ORCID; Zong, Ruiting; Nelson, David L.; Otaify, Ghada A.; Temtamy, Samia; Aglan, Mona; Issa, Mahmoud; Bönnemann, Carsten G.; Lapunzina, Pablo; Yoon, Grace; Ruiz-Pérez, Victor L. CSIC ORCID | Fecha de publicación: | 2019 | Editor: | Springer Nature | Citación: | Nature Communications 10: 797 (2019) | Resumen: | FXR1 is an alternatively spliced gene that encodes RNA binding proteins (FXR1P) involved in muscle development. In contrast to other tissues, cardiac and skeletal muscle express two FXR1P isoforms that incorporate an additional exon-15. We report that recessive mutations in this particular exon of FXR1 cause congenital multi-minicore myopathy in humans and mice. Additionally, we show that while Myf5-dependent depletion of all FXR1P isoforms is neonatal lethal, mice carrying mutations in exon-15 display non-lethal myopathies which vary in severity depending on the specific effect of each mutation on the protein. | Versión del editor: | https://doi.org/10.1038/s41467-019-08548-9 | URI: | http://hdl.handle.net/10261/189051 | DOI: | 10.1038/s41467-019-08548-9 | E-ISSN: | 2041-1723 |
Aparece en las colecciones: | (IIBM) Artículos (CABD) Artículos |
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recessmyopa.pdf | 10,82 MB | Adobe PDF | Visualizar/Abrir |
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