Generation of an iPSC line from a patient with GTP cyclohydrolase 1 (GCH1) deficiency: HDMC0061i-GCH1

Stem Cell Res. 2017 Apr:20:38-41. doi: 10.1016/j.scr.2017.02.010. Epub 2017 Feb 24.

Abstract

Fibroblasts from a female patient carrying a heterozygous variation in GTP cyclohydrolase 1 (GCH1; OMIM: 600225; HGNC: 4193; c.235_240del/p.(L79_S80del)), the rate-limiting enzyme of tetrahydrobiopterin (BH4) synthesis, were reprogrammed to iPSCs using the Cytotune®-iPS 2.0 Sendai Reprogramming Kit (Invitrogen) delivering the four reprogramming factors Oct3/4, Sox2, c-Myc and Klf4. Pluripotency of HDMC0061i-GCH1 was verified using immunohistochemistry and RT-PCR analysis. Cells differentiated spontaneously into the 3 germ layers in vitro and presented a normal karyotype. HDMC0061i-GCH1 represents the first model system to elucidate the pathomechanism underlying this rare metabolic disease and a useful tool for drug testing.

MeSH terms

  • Base Sequence
  • Cell Differentiation
  • Cell Line
  • Cellular Reprogramming*
  • DNA Mutational Analysis
  • Embryoid Bodies / metabolism
  • Embryoid Bodies / pathology
  • Female
  • Fibroblasts / cytology
  • Fibroblasts / metabolism
  • GTP Cyclohydrolase / genetics*
  • Gene Deletion
  • Humans
  • Induced Pluripotent Stem Cells / cytology*
  • Induced Pluripotent Stem Cells / metabolism
  • Karyotype
  • Kruppel-Like Factor 4
  • Microscopy, Fluorescence
  • Phenylketonurias / genetics
  • Phenylketonurias / metabolism
  • Phenylketonurias / pathology*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • KLF4 protein, human
  • Kruppel-Like Factor 4
  • Transcription Factors
  • GTP Cyclohydrolase

Supplementary concepts

  • Hyperphenylalaninemia, BH4-Deficient, B