» Articles » PMID: 33360445

Establishing a Human Embryonic Stem Cell Clone with a Heterozygous Mutation in the DGCR8 Gene

Overview
Journal Stem Cell Res
Publisher Elsevier
Specialty Cell Biology
Date 2020 Dec 28
PMID 33360445
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

DiGeorge Syndrome (DGS) Critical Region 8 (DGCR8) is a primary candidate gene in they DGS. The DGCR8 microprocessor complex subunit is an essential cofactor in the canonical miRNA biogenesis which is involved in diverse cellular functions such as cell fate decisions, apoptosis and different signaling pathways. However, the role of DGCR8 in these processes or development of DGS is not fully understood. Here we present a heterozygous DGCR8 mutant human embryonic stem cell line (HuES9) created by the CRISPR/Cas9 system. The generated HuES9 cells maintain normal karyotype, morphology, pluripotency and differentiation capacity into all three germ layers.

Citing Articles

Partial Disturbance of Microprocessor Function in Human Stem Cells Carrying a Heterozygous Mutation in the DGCR8 Gene.

Ree D, Fothi A, Varga N, Kolacsek O, Orban T, Apati A Genes (Basel). 2022; 13(11).

PMID: 36360162 PMC: 9689658. DOI: 10.3390/genes13111925.


A Novel Cell-Based Model for a Rare Disease: The Tks4-KO Human Embryonic Stem Cell Line as a Frank-Ter Haar Syndrome Model System.

Laszlo L, Maczelka H, Takacs T, Kurilla A, Tilajka A, Buday L Int J Mol Sci. 2022; 23(15).

PMID: 35955935 PMC: 9369304. DOI: 10.3390/ijms23158803.