Identification and Functional Verification of CITED2 Gene Promoter Region in Patients with Patent Ductus Arteriosus

Int J Mol Sci. 2023 Nov 11;24(22):16204. doi: 10.3390/ijms242216204.

Abstract

Patent ductus arteriosus (PDA) is a common congenital heart disease. CITED2 plays an important role in the development of the heart, and genetic variants in its coding region are significantly associated with cardiac malformations. However, the role of variants in the promoter region of CITED2 in the development of PDA remains unclear. We extracted the peripheral blood of 646 subjects (including 353 PDA patients and 293 unrelated healthy controls) for sequencing. We identified 13 promoter variants of the CITED2 gene (including 2 novel heterozygous variants). Of the 13 variants, 10 were found only in PDA patients. In mouse cardiomyocytes (HL-1) and rat cardiac myocytes (RCM), the transcriptional activity of the CITED2 gene promoter was significantly changed by the variants (p < 0.05). The results of the experiments of electrophoretic mobility indicated that these variants may affect the transcription of the CITED2 gene by influencing the binding ability of transcription factors. These results, combined with the JASPAR database analysis, showed that the destruction/production of transcription factor binding sites due to the variants in the promoter region of the CITED2 gene may directly or indirectly affect the binding ability of transcription factors. Our results suggest for the first time that variants at the CITED2 promoter region may cause low expression of CITED2 protein related to the formation of PDA.

Keywords: CITED2; gene variant; genetic; patent ductus arteriosus; promoter.

MeSH terms

  • Animals
  • Ductus Arteriosus, Patent* / genetics
  • Ductus Arteriosus, Patent* / metabolism
  • Heart Defects, Congenital* / genetics
  • Humans
  • Mice
  • Myocytes, Cardiac / metabolism
  • Promoter Regions, Genetic
  • Rats
  • Repressor Proteins / genetics
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcription Factors / genetics

Substances

  • Transcription Factors
  • CITED2 protein, human
  • Repressor Proteins
  • Trans-Activators