Departamento de Bioquímica y Biología Molecular, Facultad de Medicina, Instituto Universitario de Oncología-IUOPA, Universidad de Oviedo, 33006 Oviedo, Spain.
Genética Molecular, Red de Investigación Renal (REDINREN), 33006 Oviedo, Spain.
Nat Commun. 2014 Oct 29;5:5326. doi: 10.1038/ncomms6326.
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.
不同编码肌节蛋白的基因突变导致 50-60%的家族性肥厚型心肌病(HCM)病例;然而,目前仍有三分之一的患者的疾病遗传改变原因不明。在这里,我们描述了一例原因不明的家族性 HCM 病例。全外显子组测序显示,编码肌节蛋白细丝蛋白 C 的基因中有一个变体(p.A1539T),该变体在这个家族中与疾病共分离。对 92 例 HCM 病例的测序确定了另外七个变体,这些变体在八个家族中与疾病共分离。携带 FLNC 突变的患者心肌中存在明显的肌节异常,功能分析显示这些 FLNC 变体的表达导致大的细丝蛋白 C 聚集的形成。临床研究表明,FLNC 突变患者发生心源性猝死的几率更高。基于这些发现,我们得出结论,编码肌节蛋白细丝蛋白 C 的基因突变导致了一种新的家族性 HMC 形式。