Core planar cell polarity genes VANGL1 and VANGL2 in predisposition to congenital vertebral malformations

Proc Natl Acad Sci U S A. 2024 Apr 30;121(18):e2310283121. doi: 10.1073/pnas.2310283121. Epub 2024 Apr 26.

Abstract

Congenital scoliosis (CS), affecting approximately 0.5 to 1 in 1,000 live births, is commonly caused by congenital vertebral malformations (CVMs) arising from aberrant somitogenesis or somite differentiation. While Wnt/ß-catenin signaling has been implicated in somite development, the function of Wnt/planar cell polarity (Wnt/PCP) signaling in this process remains unclear. Here, we investigated the role of Vangl1 and Vangl2 in vertebral development and found that their deletion causes vertebral anomalies resembling human CVMs. Analysis of exome sequencing data from multiethnic CS patients revealed a number of rare and deleterious variants in VANGL1 and VANGL2, many of which exhibited loss-of-function and dominant-negative effects. Zebrafish models confirmed the pathogenicity of these variants. Furthermore, we found that Vangl1 knock-in (p.R258H) mice exhibited vertebral malformations in a Vangl gene dose- and environment-dependent manner. Our findings highlight critical roles for PCP signaling in vertebral development and predisposition to CVMs in CS patients, providing insights into the molecular mechanisms underlying this disorder.

Keywords: VANGL1/2; congenital scoliosis; congenital vertebral malformation; planar cell polarity (PCP); somite.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Carrier Proteins*
  • Cell Polarity* / genetics
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Membrane Proteins* / genetics
  • Membrane Proteins* / metabolism
  • Mice
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Scoliosis / congenital
  • Scoliosis / genetics
  • Scoliosis / metabolism
  • Spine* / abnormalities
  • Spine* / metabolism
  • Wnt Signaling Pathway / genetics
  • Zebrafish Proteins / genetics
  • Zebrafish Proteins / metabolism
  • Zebrafish* / embryology
  • Zebrafish* / genetics

Substances

  • VANGL1 protein, human
  • Membrane Proteins
  • VANGL2 protein, human
  • Zebrafish Proteins
  • vangl2 protein, zebrafish
  • Vangl1 protein, mouse
  • Ltap protein, mouse
  • Nerve Tissue Proteins
  • Intracellular Signaling Peptides and Proteins
  • Carrier Proteins