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Generation of an induced pluripotent stem cell (iPSC) line carrying a KCNA2 homozygous (p.Arg294His, R294H) mutation related to hereditary spastic paraplegia.

作者信息

Lyu Hang, Haag Carolin, Schwarz Niklas, Löffler Heidi, Mau-Holzmann Ulrike A, Lerche Holger, Rosa Filip

机构信息

Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tuebingen, Germany.

Department of Medical Genetics and Applied Genomics, University of Tuebingen, Germany.

出版信息

Stem Cell Res. 2025 Aug;86:103737. doi: 10.1016/j.scr.2025.103737. Epub 2025 May 16.

Abstract

The KCNA2 gene encodes the voltage-gated potassium channel K1.2, which is essential for repolarization of action potential. The R294H variant in KCNA2 represents the only potassium channel gene variant linked to hereditary spastic paraplegia (HSP) to date. However, this variant has been observed exclusively in heterozygous individuals. Here, we generated a homozygous KCNA2 R294H (c.881G > A) induced pluripotent stem cell (iPSC) line from a healthy individual iPSC line. The variant was introduced into both alleles using the CRISPR/Cas9 system. The resulting iPSC line has a normal karyotype, expresses key pluripotency markers, and is able to differentiate into all three germ layers.

摘要

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