Literature DB >> 25351925

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy.

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.

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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


  65 in total

1.  Loss of MT1-MMP causes cell senescence and nuclear defects which can be reversed by retinoic acid.

Authors:  Ana Gutiérrez-Fernández; Clara Soria-Valles; Fernando G Osorio; Jesús Gutiérrez-Abril; Cecilia Garabaya; Alina Aguirre; Antonio Fueyo; María Soledad Fernández-García; Xose S Puente; Carlos López-Otín
Journal:  EMBO J       Date:  2015-05-19       Impact factor: 11.598

2.  RNA sequencing-based transcriptome profiling of cardiac tissue implicates novel putative disease mechanisms in FLNC-associated arrhythmogenic cardiomyopathy.

Authors:  Charlotte L Hall; Priyatansh Gurha; Maria Sabater-Molina; Angeliki Asimaki; Marta Futema; Ruth C Lovering; Mari Paz Suárez; Beatriz Aguilera; Pilar Molina; Esther Zorio; Cristian Coarfa; Matthew J Robertson; Sirisha M Cheedipudi; Keat-Eng Ng; Paul Delaney; Juan Pedro Hernández; Francisco Pastor; Juan R Gimeno; William J McKenna; Ali J Marian; Petros Syrris
Journal:  Int J Cardiol       Date:  2019-12-06       Impact factor: 4.164

3.  Genetic basis and molecular biology of cardiac arrhythmias in cardiomyopathies.

Authors:  Ali J Marian; Babken Asatryan; Xander H T Wehrens
Journal:  Cardiovasc Res       Date:  2020-07-15       Impact factor: 10.787

4.  A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients.

Authors:  Allison L Cirino; Neal K Lakdawala; Barbara McDonough; Lauren Conner; Dale Adler; Mark Weinfeld; Patrick O'Gara; Heidi L Rehm; Kalotina Machini; Matthew Lebo; Carrie Blout; Robert C Green; Calum A MacRae; Christine E Seidman; Carolyn Y Ho
Journal:  Circ Cardiovasc Genet       Date:  2017-10

5.  Kettin, the large actin-binding protein with multiple immunoglobulin domains, is essential for sarcomeric actin assembly and larval development in Caenorhabditis elegans.

Authors:  Kanako Ono; Zhaozhao Qin; Robert C Johnsen; David L Baillie; Shoichiro Ono
Journal:  FEBS J       Date:  2019-08-24       Impact factor: 5.542

Review 6.  Translating emerging molecular genetic insights into clinical practice in inherited cardiomyopathies.

Authors:  Babken Asatryan; Argelia Medeiros-Domingo
Journal:  J Mol Med (Berl)       Date:  2018-08-20       Impact factor: 4.599

7.  Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy.

Authors:  Nathan R Tucker; Micheal A McLellan; Dongjian Hu; Jiangchuan Ye; Victoria A Parsons; Robert W Mills; Sebastian Clauss; Elena Dolmatova; Marisa A Shea; David J Milan; Nandita S Scott; Mark Lindsay; Steven A Lubitz; Ibrahim J Domian; James R Stone; Honghuang Lin; Patrick T Ellinor
Journal:  Circ Cardiovasc Genet       Date:  2017-12

8.  Primary distal renal tubular acidosis: novel findings in patients studied by next-generation sequencing.

Authors:  Juan Gómez; Helena Gil-Peña; Fernando Santos; Eliecer Coto; Ana Arango; Olaya Hernandez; Julián Rodríguez; Inmaculada Nadal; Virginia Cantos; Sara Chocrón; Inés Vergara; Álvaro Madrid; Carlos Vazquez; Luz E González; Fiona Blanco
Journal:  Pediatr Res       Date:  2015-11-16       Impact factor: 3.756

9.  Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C.

Authors:  Eyal Reinstein; Ana Gutierrez-Fernandez; Shay Tzur; Concetta Bormans; Shai Marcu; Einav Tayeb-Fligelman; Chana Vinkler; Annick Raas-Rothschild; Dana Irge; Meytal Landau; Mordechai Shohat; Xose S Puente; Doron M Behar; Carlos Lopez-Otın
Journal:  Eur J Hum Genet       Date:  2016-09-07       Impact factor: 4.246

10.  Hspb7 is a cardioprotective chaperone facilitating sarcomeric proteostasis.

Authors:  Emily J Mercer; Yi-Fan Lin; Leona Cohen-Gould; Todd Evans
Journal:  Dev Biol       Date:  2018-01-10       Impact factor: 3.582

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