Nishimura Toshiya, Fujimoto Takafumi
Faculty of Fisheries Sciences, Hokkaido University, 3-1-1 Minato, Hakodate, Hokkaido 041-8611, Japan.
iScience. 2025 Feb 8;28(3):111977. doi: 10.1016/j.isci.2025.111977. eCollection 2025 Mar 21.
In teleost fish, primordial germ cells (PGCs), the precursors of eggs and sperm, develop from cells that inherit maternal germ plasm (GP). Although numerous GP component genes have been identified, the minimum set of genes essential for germline formation remains unknown. Herein, we provide evidence that and synergistically induce PGC-like cells from the blastomeres of medaka embryos. One-cell stage embryos injected with and mRNA (DN-OE) showed developmental arrest before gastrulation and upregulation of PGC markers. Transplantation experiments revealed that most transplanted DN-OE blastomeres migrated into the gonadal ridge of host embryos, resulting in the production of functional eggs and sperm. Furthermore, the combination of genome editing and PGC induction techniques successfully generated transgenic knock-in medaka, demonstrating enhanced, precise, and stable gene integration. Identifying essential GP genes for PGC formation advances our understanding of germ cell development mechanisms and their biotechnological applications.
在硬骨鱼中,原始生殖细胞(PGCs),即卵子和精子的前体,由继承母体生殖质(GP)的细胞发育而来。尽管已鉴定出许多GP组成基因,但对于生殖系形成必不可少的最小基因集仍然未知。在此,我们提供证据表明,[基因名称1]和[基因名称2]协同诱导出了青鳉胚胎卵裂球中的类原始生殖细胞。注射了[基因名称1]和[基因名称2]mRNA(DN-OE)的单细胞期胚胎在原肠胚形成之前出现发育停滞,并上调了PGC标记物。移植实验表明,大多数移植的DN-OE卵裂球迁移到宿主胚胎的生殖嵴中,从而产生了功能性卵子和精子。此外,基因组编辑和PGC诱导技术的结合成功产生了转基因敲入青鳉,证明了增强、精确和稳定的基因整合。鉴定出对PGC形成至关重要的GP基因,有助于我们深入了解生殖细胞发育机制及其生物技术应用。