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 PMID:26301497  

Genetic association analyses highlight biological pathways underlying mitral valve prolapse.

Christian Dina | Nabila Bouatia-Naji | Nathan Tucker | Francesca N Delling | Katelynn Toomer | Ronen Durst | Maelle Perrocheau | Leticia Fernandez-Friera | Jorge Solis | PROMESA investigators | Thierry Le Tourneau | Ming-Huei Chen | Vincent Probst | Yohan Bosse | Philippe Pibarot | Diana Zelenika | Mark Lathrop | Serge Hercberg | Ronan Roussel | Emelia J Benjamin | Fabrice Bonnet | Su Hao Lo | Elena Dolmatova | Floriane Simonet | Simon Lecointe | Florence Kyndt | Richard Redon | Hervé Le Marec | Philippe Froguel | Patrick T Ellinor | Ramachandran S Vasan | Patrick Bruneval | Roger R Markwald | Russell A Norris | David J Milan | Susan A Slaugenhaupt | Robert A Levine | Jean-Jacques Schott | Albert A Hagege | MVP-France | Xavier Jeunemaitre | Leducq Transatlantic MITRAL Network
Nature genetics | 2015

Nonsyndromic mitral valve prolapse (MVP) is a common degenerative cardiac valvulopathy of unknown etiology that predisposes to mitral regurgitation, heart failure and sudden death. Previous family and pathophysiological studies suggest a complex pattern of inheritance. We performed a meta-analysis of 2 genome-wide association studies in 1,412 MVP cases and 2,439 controls. We identified 6 loci, which we replicated in 1,422 cases and 6,779 controls, and provide functional evidence for candidate genes. We highlight LMCD1 (LIM and cysteine-rich domains 1), which encodes a transcription factor and for which morpholino knockdown of the ortholog in zebrafish resulted in atrioventricular valve regurgitation. A similar zebrafish phenotype was obtained with knockdown of the ortholog of TNS1, which encodes tensin 1, a focal adhesion protein involved in cytoskeleton organization. We also showed expression of tensin 1 during valve morphogenesis and describe enlarged posterior mitral leaflets in Tns1(-/-) mice. This study identifies the first risk loci for MVP and suggests new mechanisms involved in mitral valve regurgitation, the most common indication for mitral valve repair.

Pubmed ID: 26301497

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: Canadian Institutes of Health Research, Canada
    Id: MOP-137058
  • Agency: Canadian Institutes of Health Research, Canada
    Id: MOP-126072
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL109506
  • Agency: NHLBI NIH HHS, United States
    Id: R01-HL127692
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL127692
  • Agency: Canadian Institutes of Health Research, Canada
    Id: MOP-114997
  • Agency: NHLBI NIH HHS, United States
    Id: K24HL105780
  • Agency: NIGMS NIH HHS, United States
    Id: 8P20 GM103444-07
  • Agency: NHLBI NIH HHS, United States
    Id: HL065962
  • Agency: NHLBI NIH HHS, United States
    Id: K24 HL67434
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL128099
  • Agency: NHLBI NIH HHS, United States
    Id: T32 HL007208
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL72265
  • Agency: NHLBI NIH HHS, United States
    Id: HL109506
  • Agency: Canadian Institutes of Health Research, Canada
    Id: MOP-102481
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL109004
  • Agency: Canadian Institutes of Health Research, Canada
    Id: MOP-102737
  • Agency: NCRR NIH HHS, United States
    Id: C06 RR018823
  • Agency: NIGMS NIH HHS, United States
    Id: 1P30 GM103342
  • Agency: NHLBI NIH HHS, United States
    Id: K23 HL116652
  • Agency: NHLBI NIH HHS, United States
    Id: R01-HL33756
  • Agency: NHLBI NIH HHS, United States
    Id: HL092577
  • Agency: NHLBI NIH HHS, United States
    Id: HL104156

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This is a list of tools and resources that we have found mentioned in this publication.


PLINK (tool)

RRID:SCR_001757

Open source whole genome association analysis toolset, designed to perform range of basic, large scale analyses in computationally efficient manner. Used for analysis of genotype/phenotype data. Through integration with gPLINK and Haploview, there is some support for subsequent visualization, annotation and storage of results. PLINK 1.9 is improved and second generation of the software.

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METAL (tool)

RRID:SCR_002013

Software application designed to facilitate meta-analysis of large datasets (such as several whole genome scans) in a convenient, rapid and memory efficient manner. (entry from Genetic Analysis Software)

View all literature mentions

IMPUTE (tool)

RRID:SCR_009245

Software application for estimating (imputing) unobserved genotypes in SNP association studies. The program is designed to work seamlessly with the output of the genotype calling program CHIAMO and the population genetic simulator HAPGEN, and it produces output that can be analyzed using the program SNPTEST. (entry from Genetic Analysis Software)

View all literature mentions

MACH (tool)

RRID:SCR_009621

QTL analysis based on imputed dosages/posterior_probabilities.

View all literature mentions