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Novel mutations in MYBPC1 are associated with myogenic tremor and mild myopathy
Author(s) -
Stavusis Janis,
Lace Baiba,
Schäfer Jochen,
Geist Janelle,
Inashkina Inna,
Kidere Dita,
Pajusalu Sander,
Wright Nathan T.,
Saak Annika,
Weinhold Manja,
Haubenberger Dietrich,
Jackson Sandra,
KontrogianniKonstantopoulos Aikaterini,
Bönnemann Carsten G.
Publication year - 2019
Publication title -
annals of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.764
H-Index - 296
eISSN - 1531-8249
pISSN - 0364-5134
DOI - 10.1002/ana.25494
Subject(s) - missense mutation , myopathy , genetics , phenotype , biology , myosin , mutation , genetic heterogeneity , exome sequencing , genetic counseling , gene , microbiology and biotechnology
Objective To define a distinct, dominantly inherited, mild skeletal myopathy associated with prominent and consistent tremor in two unrelated, three‐generation families. Methods Clinical evaluations as well as exome and panel sequencing analyses were performed in affected and nonaffected members of two families to identify genetic variants segregating with the phenotype. Histological assessment of a muscle biopsy specimen was performed in 1 patient, and quantitative tremor analysis was carried out in 2 patients. Molecular modeling studies and biochemical assays were performed for both mutations. Results Two novel missense mutations in MYBPC1 (p.E248K in family 1 and p.Y247H in family 2) were identified and shown to segregate perfectly with the myopathy/tremor phenotype in the respective families. MYBPC1 encodes slow myosin binding protein‐C (sMyBP‐C), a modular sarcomeric protein playing structural and regulatory roles through its dynamic interaction with actin and myosin filaments. The Y247H and E248K mutations are located in the NH 2 ‐terminal M‐motif of sMyBP‐C. Both mutations result in markedly increased binding of the NH 2 terminus to myosin, possibly interfering with normal cross‐bridge cycling as the first muscle‐based step in tremor genesis. The clinical tremor features observed in all mutation carriers, together with the tremor physiology studies performed in family 2, suggest amplification by an additional central loop modulating the clinical tremor phenomenology. Interpretation Here, we link two novel missense mutations in MYBPC1 with a dominant, mild skeletal myopathy invariably associated with a distinctive tremor. The molecular, genetic, and clinical studies are consistent with a unique sarcomeric origin of the tremor, which we classify as “myogenic tremor.” ANN NEUROL 2019