Protein haploinsufficiency drivers identify MYBPC3 variants that cause hypertrophic cardiomyopathy

Suay-Corredera C. ; Pricolo M.R. ; Herrero-Galán E. ; Velázquez-Carreras D. ; Sánchez-Ortiz D. ; García-Giustiniani D. ; Delgado J. ; Galano-Frutos J.J. ; García Cebollada H. (Universidad de Zaragoza) ; Vilches S. ; Domínguez F. ; Molina M.S. ; Barriales-Villa R. ; Frisso G. ; Sancho Sanz J. (Universidad de Zaragoza) ; Serrano L. ; García-Pavía P. ; Monserrat L. ; Alegre-Cebollada J.

Resumen: Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disease. Variants in MYBPC3, the gene encoding cardiac myosin-binding protein C (cMyBP-C), are the leading cause of HCM. However, the pathogenicity status of hundreds of MYBPC3 variants found in patients remains unknown, as a consequence of our incomplete understanding of the pathomechanisms triggered by HCM-causing variants. Here, we examined 44 nontruncating MYBPC3 variants that we classified as HCM-linked or nonpathogenic according to cosegregation and population genetics criteria. We found that around half of the HCM-linked variants showed alterations in RNA splicing or protein stability, both of which can lead to cMyBP-C haploinsufficiency. These protein haploinsufficiency drivers associated with HCM pathogenicity with 100% and 94% specificity, respectively. Furthermore, we uncovered that 11% of nontruncating MYBPC3 variants currently classified as of uncertain significance in ClinVar induced one of these molecular phenotypes. Our strategy, which can be applied to other conditions induced by protein loss of function, supports the idea that cMyBP-C haploinsufficiency is a fundamental pathomechanism in HCM. © 2021 THE AUTHORS.

Idioma: Inglés

DOI: 10.1016/j.jbc.2021.100854

Año: 2021

Publicado en: Journal of Biological Chemistry 297, 1 (2021), 100854 [14 pp]
ISSN: 0021-9258

Factor impacto JCR: 5.485 (2021)

Categ. JCR: BIOCHEMISTRY & MOLECULAR BIOLOGY rank: 94 / 297 = 0.316 (2021) - Q2 - T1

Factor impacto CITESCORE: 8.8 - Biochemistry, Genetics and Molecular Biology (Q1)

Factor impacto SCIMAGO: 1.871 - Cell Biology (Q1) - Biochemistry (Q1)

Tipo y forma: Artículo (Versión definitiva)

Área (Departamento): Área Bioquímica y Biolog.Mole. (Dpto. Bioq.Biolog.Mol. Celular)