Genetic screening and multipotency in rhesus monkey haploid neural progenitor cells.
Haisong WangWenhao ZhangJian YuCongyu WuQian GaoXu LiYanni LiJinxin ZhangYaru TianTao TanWeizhi JiLuyuan LiYang YuLing ShuaiPublished in: Development (Cambridge, England) (2018)
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.
Keyphrases
- embryonic stem cells
- copy number
- genome wide
- crispr cas
- endothelial cells
- dna methylation
- high throughput
- genome editing
- induced pluripotent stem cells
- induced apoptosis
- multidrug resistant
- genome wide identification
- spinal cord
- cell proliferation
- emergency department
- human health
- cell cycle arrest
- risk assessment
- pluripotent stem cells
- intellectual disability
- signaling pathway
- climate change
- drug induced