Generation of a WA14 hESC sub-line carrying a hemizygous ABCD1 (C.1696_1710 del) mutation introduced by CRISPR/Cas9 technology

Summary

ATP-binding cassette transporter subfamily D member 1 (ABCD1) gene is a member of ABC transporter super family, which conduct peroxisomal import of very long chain fatty acid and crucial underlying factor that induces X-linked adrenoleukodystrophy (X-ALD) when the gene is defected. Here, we report the generation of a human embryonic stem cell sub-line harboring a hemizygous ABCD1 mutation (C.1696_1710 del) using CRISPR/Cas9 system. Established line expresses pluripotency marker genes, can be differentiated to three germ layers, and maintains a normal karyotype. Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.

Authors Hong W, Yun W, Choi W, Son D, Song G, You S
Journal Stem cell research
Publication Date 2021 Feb 11;52:102244
PubMed 33611043
DOI 10.1016/j.scr.2021.102244

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