Wang Bo, Collins James J, Newmark Phillip A
Howard Hughes Medical Institute, University of Illinois at Urbana-Champaign , Urbana , United States ; Institute for Genomic Biology , University of Illinois at Urbana-Champaign , Urbana , United States.
Elife. 2013 Jul 30;2:e00768. doi: 10.7554/eLife.00768.
Schistosomes infect hundreds of millions of people in the developing world. Transmission of these parasites relies on a stem cell-driven, clonal expansion of larvae inside a molluscan intermediate host. How this novel asexual reproductive strategy relates to current models of stem cell maintenance and germline specification is unclear. Here, we demonstrate that this proliferative larval cell population (germinal cells) shares some molecular signatures with stem cells from diverse organisms, in particular neoblasts of planarians (free-living relatives of schistosomes). We identify two distinct germinal cell lineages that differ in their proliferation kinetics and expression of a nanos ortholog. We show that a vasa/PL10 homolog is required for proliferation and maintenance of both populations, whereas argonaute2 and a fibroblast growth factor receptor-encoding gene are required only for nanos-negative cells. Our results suggest that an ancient stem cell-based developmental program may have enabled the evolution of the complex life cycle of parasitic flatworms. DOI:http://dx.doi.org/10.7554/eLife.00768.001.
血吸虫感染了发展中世界数亿人口。这些寄生虫的传播依赖于在软体动物中间宿主体内由干细胞驱动的幼虫克隆性扩增。这种新型无性生殖策略与当前干细胞维持和生殖系特化模型之间的关系尚不清楚。在此,我们证明这种增殖性幼虫细胞群体(生殖细胞)与来自不同生物体的干细胞具有一些分子特征,特别是涡虫(血吸虫的自由生活近亲)的新成细胞。我们鉴定出两个不同的生殖细胞谱系,它们在增殖动力学和一个nanos直系同源基因的表达上存在差异。我们表明,一个vasa/PL10同源物是这两个群体增殖和维持所必需的,而AGO2和一个成纤维细胞生长因子受体编码基因仅对nanos阴性细胞是必需的。我们的结果表明,一个基于古老干细胞的发育程序可能促成了寄生扁虫复杂生命周期的进化。DOI:http://dx.doi.org/10.7554/eLife.00768.001