| Literature DB >> 29784672 |
Haisong Wang1, Wenhao Zhang1, Jian Yu2, Congyu Wu3, Qian Gao1,4, Xu Li1, Yanni Li1, Jinxin Zhang1, Yaru Tian1, Tao Tan5, Weizhi Ji5, Luyuan Li1, Yang Yu4, Ling Shuai6.
Abstract
Haploid embryonic stem cells (haESCs) have been extensively applied in forward and reverse genetic screening. However, a mammalian haploid somatic cell line is difficult to achieve because of spontaneous diploidization in differentiation. As a non-human primate species, monkeys are widely used in basic and pre-clinical research in which haploid cells are restricted to ESCs. Here, we report that rhesus monkey haESCs in an optimized culture medium show naïve-state pluripotency and stable haploidy. This model facilitated the derivation of haploid neural progenitor cells (haNPCs), which maintained haploidy and differentiation potential into neurons and glia for a long period in vitro High-throughput trapping mutations can be efficiently introduced into haNPCs via piggyBac transposons. This system proves useful when identifying gene targets of neural toxicants via a proof-of-concept experiment. Using CRISPR/Cas9 editing, we confirmed that B4GALT6, from the candidate gene list, is a resistance gene of A803467 (a tetrodotoxin-like toxicant). This model is the first non-human primate haploid somatic cell line with proliferative ability, multipotency and an intact genome, thus providing a cellular resource for recessive genetic and potential drug screening.Entities:
Keywords: Genetic screening; Haploid NPCs; Monkey; Naïve pluripotency
Mesh:
Substances:
Year: 2018 PMID: 29784672 DOI: 10.1242/dev.160531
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868