Literature DB >> 33360445

Establishing a human embryonic stem cell clone with a heterozygous mutation in the DGCR8 gene.

Dóra Reé1, Adrienn Borsy1, Ábel Fóthi1, Tamás I Orbán1, György Várady1, Zsuzsa Erdei1, Balázs Sarkadi1, János Réthelyi2, Nóra Varga1, Ágota Apáti3.   

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 (HuES9DGCR8+/-) created by the CRISPR/Cas9 system. The generated HuES9DGCR8+/- cells maintain normal karyotype, morphology, pluripotency and differentiation capacity into all three germ layers.
Copyright © 2020 The Author(s). Published by Elsevier B.V. All rights reserved.

Entities:  

Year:  2020        PMID: 33360445     DOI: 10.1016/j.scr.2020.102134

Source DB:  PubMed          Journal:  Stem Cell Res        ISSN: 1873-5061            Impact factor:   2.020


  1 in total

1.  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.

Authors:  Loretta László; Hédi Maczelka; Tamás Takács; Anita Kurilla; Álmos Tilajka; László Buday; Virag Vas; Ágota Apáti
Journal:  Int J Mol Sci       Date:  2022-08-08       Impact factor: 6.208

  1 in total

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