Genetic abnormalities in FOXP1 are associated with congenital heart defects

Hum Mutat. 2013 Sep;34(9):1226-30. doi: 10.1002/humu.22366. Epub 2013 Jul 11.

Abstract

The etiology for the majority of congenital heart defects (CHD) is unknown. We identified a patient with unbalanced atrioventricular septal defect (AVSD) and hypoplastic left ventricle who harbored an ~0.3 Mb monoallelic deletion on chromosome 3p14.1. The deletion encompassed the first four exons of FOXP1, a gene critical for normal heart development that represses cardiomyocyte proliferation and expression of Nkx2.5. To determine whether FOXP1 mutations are found in patients with CHD, we sequenced FOXP1 in 82 patients with AVSD or hypoplastic left heart syndrome. We discovered two patients who harbored a heterozygous c.1702C>T variant in FOXP1 that predicted a potentially deleterious substitution of a highly conserved proline (p.Pro568Ser). This variant was not found in 287 controls but is present in dbSNP at a 0.2% frequency. The orthologous murine Foxp1 p.Pro596Ser mutant protein displayed deficits in luciferase reporter assays and resulted in increased proliferation and Nkx2.5 expression in cardiomyoblasts. Our data suggest that haploinsufficiency of FOXP1 is associated with human CHD.

Keywords: FOXP1; atrioventricular septal defect; cardiomyocyte; hypoplastic left heart syndrome.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Chromosomes, Human, Pair 3
  • Forkhead Transcription Factors / genetics*
  • Forkhead Transcription Factors / metabolism*
  • Gene Frequency
  • Genetic Association Studies
  • Genetic Variation
  • Haploinsufficiency
  • Heart Defects, Congenital / genetics*
  • Heart Defects, Congenital / metabolism
  • Heart Septal Defects / genetics*
  • Homeobox Protein Nkx-2.5
  • Homeodomain Proteins / metabolism
  • Humans
  • Hypoplastic Left Heart Syndrome / genetics*
  • Infant, Newborn
  • Mice
  • Molecular Sequence Data
  • Myoblasts, Cardiac / metabolism*
  • Polymorphism, Single Nucleotide
  • Repressor Proteins / genetics*
  • Repressor Proteins / metabolism*
  • Sequence Deletion
  • Transcription Factors / metabolism

Substances

  • FOXP1 protein, human
  • Forkhead Transcription Factors
  • Foxp1 protein, mouse
  • Homeobox Protein Nkx-2.5
  • Homeodomain Proteins
  • NKX2-5 protein, human
  • Repressor Proteins
  • Transcription Factors

Supplementary concepts

  • Atrioventricular Septal Defect