| Literature DB >> 25351925 |
Rafael Valdés-Mas1, Ana Gutiérrez-Fernández1, Juan Gómez2, Eliecer Coto3, Aurora Astudillo4, Diana A Puente1, Julián R Reguero5, Victoria Álvarez2, César Morís6, Diego León5, María Martín5, Xose S Puente1, Carlos López-Otín1.
Abstract
Mutations in different genes encoding sarcomeric proteins are responsible for 50-60% of familial cases of hypertrophic cardiomyopathy (HCM); however, the genetic alterations causing the disease in one-third of patients are currently unknown. Here we describe a case with familial HCM of unknown cause. Whole-exome sequencing reveals a variant in the gene encoding the sarcomeric protein filamin C (p.A1539T) that segregates with the disease in this family. Sequencing of 92 HCM cases identifies seven additional variants segregating with the disease in eight families. Patients with FLNC mutations show marked sarcomeric abnormalities in cardiac muscle, and functional analysis reveals that expression of these FLNC variants resulted in the formation of large filamin C aggregates. Clinical studies indicate that FLNC-mutated patients have higher incidence of sudden cardiac death. On the basis of these findings, we conclude that mutations in the gene encoding the sarcomeric protein filamin C cause a new form of familial HMC.Entities:
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Year: 2014 PMID: 25351925 DOI: 10.1038/ncomms6326
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919