NKX2-1 mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in "Brain-Lung-Thyroid Syndrome"

Hum Mutat. 2010 Feb;31(2):E1146-62. doi: 10.1002/humu.21183.

Abstract

NKX2-1 (NK2 homeobox 1) is a critical regulator of transcription for the surfactant protein (SP)-B and -C genes (SFTPB and SFTPC, respectively). We identified and functionally characterized two new de novo NKX2-1 mutations c.493C>T (p.R165W) and c.786_787del2 (p.L263fs) in infants with closely similar severe interstitial lung disease (ILD), hypotonia, and congenital hypothyroidism. Functional analyses using A549 and HeLa cells revealed that NKX2-1-p.L263fs induced neither SFTPB nor SFTPC promoter activation and had a dominant negative effect on wild-type (WT) NKX2-1. In contrast,NKX2-1-p.R165W activated SFTPC, to a significantly greater extent than did WTNKX2-1, while SFTPB activation was only significantly reduced in HeLa cells. In accordance with our in vitro data, we found decreased amounts of SP-B and SP-C by western blot in bronchoalveolar lavage fluid (patient with p.L263fs) and features of altered surfactant protein metabolism on lung histology (patient with NKX2-1-p.R165W). In conclusion, ILD in patients with NKX2-1 mutations was associated with altered surfactant protein metabolism, and both gain and loss of function of the mutated NKX2-1 genes on surfactant protein promoters were associated with ILD in "Brain-Lung-Thyroid syndrome".

Publication types

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

MeSH terms

  • Abnormalities, Multiple / diagnostic imaging
  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / pathology
  • Amino Acid Sequence
  • Base Sequence
  • Bronchoalveolar Lavage Fluid
  • Cell Line, Tumor
  • Child
  • Child, Preschool
  • DNA
  • Fatal Outcome
  • Female
  • Gene Expression Regulation*
  • Humans
  • Infant
  • Infant, Newborn
  • Lung Diseases, Interstitial / complications
  • Lung Diseases, Interstitial / diagnostic imaging
  • Lung Diseases, Interstitial / genetics*
  • Lung Diseases, Interstitial / pathology
  • Molecular Sequence Data
  • Mutant Proteins / chemistry
  • Mutant Proteins / metabolism
  • Mutation / genetics*
  • Nuclear Proteins / chemistry
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Organ Specificity / genetics
  • Pregnancy
  • Promoter Regions, Genetic / genetics*
  • Protein Binding
  • Pulmonary Surfactant-Associated Proteins / genetics*
  • Radiography
  • Syndrome
  • Thyroid Gland / pathology
  • Thyroid Nuclear Factor 1
  • Transcription Factors / chemistry
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism

Substances

  • Mutant Proteins
  • Nuclear Proteins
  • Pulmonary Surfactant-Associated Proteins
  • Thyroid Nuclear Factor 1
  • Transcription Factors
  • DNA