斑马鱼
生物
卵裂球
种质资源
基因组编辑
囊胚
转录激活物样效应核酸酶
基因组
移植
清脆的
遗传学
胚层
胚胎干细胞
胚胎
细胞生物学
原肠化
基因
胚胎发生
内科学
医学
农学
作者
Xiaosi Wang,Junwen Zhu,Houpeng Wang,Wenqi Deng,Shengbo Jiao,Yaqing Wang,Mudan He,Fenghua Zhang,Tao Liu,Yongkang Hao,Ding Ye,Yuhan Sun
标识
DOI:10.1038/s41467-023-43587-3
摘要
Abstract The combination of genome editing and primordial germ cell (PGC) transplantation has enormous significance in the study of developmental biology and genetic breeding, despite its low efficiency due to limited number of donor PGCs. Here, we employ a combination of germplasm factors to convert blastoderm cells into induced PGCs (iPGCs) in zebrafish and obtain functional gametes either through iPGC transplantation or via the single blastomere overexpression of germplasm factors. Zebrafish-derived germplasm factors convert blastula cells of Gobiocypris rarus into iPGCs, and Gobiocypris rarus spermatozoa can be produced by iPGC-transplanted zebrafish. Moreover, the combination of genome knock-in and iPGC transplantation perfectly resolves the contradiction between high knock-in efficiency and early lethality during embryonic stages and greatly improves the efficiency of genome knock-in. Together, we present an efficient method for generating PGCs in a teleost, a technique that will have a strong impact in basic research and aquaculture.
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