Generation of an induced pluripotent stem cell line (IUFi001) from a Cockayne syndrome patient carrying a mutation in the ERCC6 gene

Stem Cell Res. 2021 Aug:55:102456. doi: 10.1016/j.scr.2021.102456. Epub 2021 Jul 7.

Abstract

Human fibroblasts from a Cockayne Syndrome (CS) patient carrying the compound heterozygous c.1131 A > T and c.2571C > T within ERCC Excision Repair 6 (ERCC6) were reprogramed to generate integration-free induced pluripotent stem cells (iPSCs). Characterization of IUFi001-iPSCs demonstrated that this iPSC line is free of exogenous reprogrammed genes and maintains the genomic integrity. The pluripotency of IUFi001-iPSCs was confirmed by the expression of the pluripotency-associated markers and by embryoid body-based differentiation into cell types representative of the three germ layers. The generated iPSC line provides a powerful tool to dissect the molecular mechanisms underlying CS caused by mutations within ERCC6.

MeSH terms

  • Cell Differentiation
  • Cockayne Syndrome* / genetics
  • DNA Helicases
  • DNA Repair Enzymes
  • Embryoid Bodies
  • Humans
  • Induced Pluripotent Stem Cells*
  • Mutation
  • Poly-ADP-Ribose Binding Proteins

Substances

  • Poly-ADP-Ribose Binding Proteins
  • DNA Helicases
  • ERCC6 protein, human
  • DNA Repair Enzymes