Li Qian, Fujii Wataru, Naito Kunihiko, Yoshizaki Goro
Department of Marine Biosciences, Tokyo University of Marine Science and Technology, Tokyo, Japan.
Department of Animal Resource Sciences, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.
Mol Reprod Dev. 2017 Oct;84(10):1100-1111. doi: 10.1002/mrd.22870. Epub 2017 Aug 11.
Germ cell transplantation is a promising technology for the propagation of endangered or valuable fishes. In this technique, sterile male and female recipient fish are injected with donor germ cells so they can produce viable gametes derived from the donor cells. The dead end (dnd) gene is involved in the migration of primordial germ cells; therefore, dnd-knockout zebrafish are expected to be germ-cell-free, making them suitable recipients for germ cell transplantation. dnd mutants were produced by microinjecting 2 nl of 10 ng/μl cRNAs encoding zinc finger nucleases against dnd into the blastodisc of zebrafish embryos before the cell- cleavage stage. One of the resulting founder males was mated with a wild-type female, and produced heterozygous mutants in the F1 generation. Mating of these F1 mutants produced an F2 generation with approximately 25% of the clutch being homozygous mutant (dnd-knockout) male, and lacking germ cells (as confirmed by expression analyses of vasa). The resulting dnd-knockout zebrafish males were tested for suitability as germ cell transplantation recipients by intraperitoneal transplantation of testicular cells prepared from vasa-gfp zebrafish. GFP-positive germ cells incorporated into the germ-cell-free gonads of the dnd-knockout recipients matured into functional sperm. Progeny tests revealed that the sperm from these dnd-knockout recipients were derived entirely from donor cells. Thus, we demonstrated that homozygous dnd mutants became germ-cell-free males that are able to nurse donor-derived germ cells.
生殖细胞移植是一种用于濒危或有价值鱼类繁殖的有前景的技术。在这项技术中,向不育的雄性和雌性受体鱼注射供体生殖细胞,以便它们能够产生源自供体细胞的可存活配子。死亡末端(dnd)基因参与原始生殖细胞的迁移;因此,预计dnd基因敲除的斑马鱼没有生殖细胞,使其成为生殖细胞移植的合适受体。通过在细胞分裂阶段之前将2微升10纳克/微升编码针对dnd的锌指核酸酶的cRNA显微注射到斑马鱼胚胎的胚盘中来产生dnd突变体。其中一只产生的奠基雄性与野生型雌性交配,并在F1代产生杂合突变体。这些F1突变体交配产生F2代,其中约25%的一窝是纯合突变体(dnd基因敲除)雄性,并且缺乏生殖细胞(通过vasa的表达分析证实)。通过对从vasa - gfp斑马鱼制备的睾丸细胞进行腹腔移植,测试产生的dnd基因敲除斑马鱼雄性作为生殖细胞移植受体的适用性。GFP阳性生殖细胞整合到dnd基因敲除受体的无生殖细胞性腺中,成熟为功能性精子。后代测试表明,这些dnd基因敲除受体的精子完全源自供体细胞。因此,我们证明了纯合dnd突变体成为能够哺育供体来源生殖细胞的无生殖细胞雄性。