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Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathy

2019; Elsevier BV; Volume: 21; Issue: 11 Linguagem: Inglês

10.1038/s41436-019-0532-z

1530-0366

René G. Feichtinger, Bettina E. Mucha, Holger Hengel, Zakaria Orfi, Christine Makowski, Junio Dort, Guy D’Anjou, Thi Tuyet Mai Nguyen, Rebecca Buchert, Hendrik Juenger, Peter Freisinger, Sarah Baumeister, Benedikt Schoser, Uwe Ahting, Reinhard Keimer, Cam‐Tu Émilie Nguyen, Paul Fabre, Julie Gauthier, Marguerite Miguet, Fátima Lopes, Afnan AlHakeem, Amal Alhashem, Brahim Tabarki, Krishna Kumar Kandaswamy, Peter Bauer, Peter Steinbacher, Holger Prokisch, Marc Sturm, Tim M. Strom, Benjamin Ellezam, Johannes A. Mayr, Lüdger Schöls, Jacques L. Michaud, Philippe M. Campeau, Tobias B. Haack, Nicolas A. Dumont,

Tissue Engineering and Regenerative Medicine

PurposeSkeletal muscle growth and regeneration rely on muscle stem cells, called satellite cells. Specific transcription factors, particularly PAX7, are key regulators of the function of these cells. Knockout of this factor in mice leads to poor postnatal survival; however, the consequences of a lack of PAX7 in humans have not been established.MethodsHere, we study five individuals with myopathy of variable severity from four unrelated consanguineous couples. Exome sequencing identified pathogenic variants in the PAX7 gene. Clinical examination, laboratory tests, and muscle biopsies were performed to characterize the disease.ResultsThe disease was characterized by hypotonia, ptosis, muscular atrophy, scoliosis, and mildly dysmorphic facial features. The disease spectrum ranged from mild to severe and appears to be progressive. Muscle biopsies showed the presence of atrophic fibers and fibroadipose tissue replacement, with the absence of myofiber necrosis. A lack of PAX7 expression was associated with satellite cell pool exhaustion; however, the presence of residual myoblasts together with regenerating myofibers suggest that a population of PAX7-independent myogenic cells partially contributes to muscle regeneration.ConclusionThese findings show that biallelic variants in the master transcription factor PAX7 cause a new type of myopathy that specifically affects satellite cell survival.