MCB Department, Brown University, 185 Meeting Street, BOX-GL173, Providence, RI 02912, USA.
Development. 2011 Jan;138(2):237-43. doi: 10.1242/dev.054940.
Many indirect developing animals create specialized multipotent cells in early development to construct the adult body and perhaps to hold the fate of the primordial germ cells. In sea urchin embryos, small micromeres formed at the fifth division appear to be such multipotent cells: they are relatively quiescent in embryos, but contribute significantly to the coelomic sacs of the larvae, from which the major tissues of the adult rudiment are derived. These cells appear to be regulated by a conserved gene set that includes the classic germline lineage genes vasa, nanos and piwi. In vivo lineage mapping of the cells awaits genetic manipulation of the lineage, but previous research has demonstrated that the germline is not specified at the fourth division because animals are fertile even when micromeres, the parent blastomeres of small micromeres, are deleted. Here, we have deleted small micromeres at the fifth division and have raised the resultant larvae to maturity. These embryos developed normally and did not overexpress Vasa, as did embryos from a micromere deletion, implying the compensatory gene regulatory network was not activated in small micromere-deleted embryos. Adults from control and micromere-deleted embryos developed gonads and visible gametes, whereas small micromere-deleted animals formed small gonads that lacked gametes. Quantitative PCR results indicate that small micromere-deleted animals produce background levels of germ cell products, but not specifically eggs or sperm. These results suggest that germline specification depends on the small micromeres, either directly as lineage products, or indirectly by signaling mechanisms emanating from the small micromeres or their descendants.
许多间接发育的动物在早期发育中产生专门的多能细胞,以构建成体,并可能维持原始生殖细胞的命运。在海胆胚胎中,第五次分裂形成的小极细胞似乎就是这种多能细胞:它们在胚胎中相对静止,但对幼虫的体腔囊有很大的贡献,体腔囊是成年原基的主要组织来源。这些细胞似乎受到一个保守的基因集的调控,其中包括经典的生殖系谱系基因 vasa、nanos 和 piwi。这些细胞的体内谱系追踪有待于对谱系进行遗传操作,但之前的研究表明,生殖系在第四次分裂时并未特化,因为即使极细胞(小极细胞的亲代分裂球)被删除,动物仍然具有生育能力。在这里,我们在第五次分裂时删除了小极细胞,并将得到的幼虫饲养成熟。这些胚胎发育正常,不像微细胞缺失胚胎那样过度表达 Vasa,这意味着小极细胞缺失胚胎中的补偿性基因调控网络没有被激活。来自对照和微细胞缺失胚胎的成体形成了性腺和可见的配子,而小极细胞缺失动物形成了缺乏配子的小性腺。定量 PCR 结果表明,小极细胞缺失动物产生背景水平的生殖细胞产物,但不是专门的卵子或精子。这些结果表明,生殖系特化取决于小极细胞,要么作为谱系产物直接特化,要么通过从小极细胞或其后代发出的信号机制间接特化。