A human FLII gene variant alters sarcomeric actin thin filament length and predisposes to cardiomyopathy

Proc Natl Acad Sci U S A. 2023 May 9;120(19):e2213696120. doi: 10.1073/pnas.2213696120. Epub 2023 May 1.

Abstract

To better understand the genetic basis of heart disease, we identified a variant in the Flightless-I homolog (FLII) gene that generates a R1243H missense change and predisposes to cardiac remodeling across multiple previous human genome-wide association studies (GWAS). Since this gene is of unknown function in the mammalian heart we generated gain- and loss-of-function genetically altered mice, as well as knock-in mice with the syntenic R1245H amino acid substitution, which showed that Flii protein binds the sarcomeric actin thin filament and influences its length. Deletion of Flii from the heart, or mice with the R1245H amino acid substitution, show cardiomyopathy due to shortening of the actin thin filaments. Mechanistically, Flii is a known actin binding protein that we show associates with tropomodulin-1 (TMOD1) to regulate sarcomere thin filament length. Indeed, overexpression of leiomodin-2 in the heart, which lengthens the actin-containing thin filaments, partially rescued disease due to heart-specific deletion of Flii. Collectively, the identified FLII human variant likely increases cardiomyopathy risk through an alteration in sarcomere structure and associated contractile dynamics, like other sarcomere gene-based familial cardiomyopathies.

Keywords: actin thin filament; cardiomyopathy; heart; sarcomere.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Actin Cytoskeleton / metabolism
  • Actins* / metabolism
  • Animals
  • Cardiomyopathies* / metabolism
  • Cytoskeletal Proteins / metabolism
  • Genome-Wide Association Study
  • Humans
  • Mammals / genetics
  • Mice
  • Microfilament Proteins / metabolism
  • Muscle Proteins / metabolism
  • Sarcomeres / metabolism
  • Trans-Activators / metabolism
  • Tropomodulin / metabolism

Substances

  • Actins
  • FLII protein, human
  • Microfilament Proteins
  • Trans-Activators
  • TMOD1 protein, human
  • Tropomodulin
  • leiomodin protein, mouse
  • Cytoskeletal Proteins
  • Muscle Proteins
  • FlII protein, mouse