Generation of a gene corrected human isogenic iPSC line (CPGHi001-A-1) from a hearing loss patient with the TMC1 p.M418K mutation using CRISPR/Cas9

Stem Cell Res. 2022 Apr:60:102736. doi: 10.1016/j.scr.2022.102736. Epub 2022 Feb 28.

Abstract

TMC1 p.M418K mutation is homologous to that in Beethoven mice, which may induce autosomal dominant non-syndromic progressive hearing loss. Previously, we generated an induced pluripotent stem cells (iPSCs) line (CPGHi001-A) from a hearing loss patient with the TMC1 c.1253 T > A (p.M418K) mutation. Here we genetically corrected the TMC1 c.1253 T > A mutation using CRISPR/Cas9 technology to generate an isogenic control, CPGHi001-A-1. The resulting iPSCs had a normal karyotype, showed pluripotency by immunofluorescence staining, and differentiated into the three germ layers in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CRISPR-Cas Systems / genetics
  • Cell Differentiation
  • Hearing Loss* / genetics
  • Humans
  • Induced Pluripotent Stem Cells*
  • Membrane Proteins / genetics
  • Mice
  • Mutation / genetics

Substances

  • Membrane Proteins
  • TMC1 protein, human
  • TMC1 protein, mouse