Saberi Amir, Jamal Ayana, Beets Isabel, Schoofs Liliane, Newmark Phillip A
Howard Hughes Medical Institute and Department of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States of America.
Department of Biology, Functional Genomics and Proteomics Unit, KU Leuven, Leuven, Belgium.
PLoS Biol. 2016 May 10;14(5):e1002457. doi: 10.1371/journal.pbio.1002457. eCollection 2016 May.
Planarians display remarkable plasticity in maintenance of their germline, with the ability to develop or dismantle reproductive tissues in response to systemic and environmental cues. Here, we investigated the role of G protein-coupled receptors (GPCRs) in this dynamic germline regulation. By genome-enabled receptor mining, we identified 566 putative planarian GPCRs and classified them into conserved and phylum-specific subfamilies. We performed a functional screen to identify NPYR-1 as the cognate receptor for NPY-8, a neuropeptide required for sexual maturation and germ cell differentiation. Similar to NPY-8, knockdown of this receptor results in loss of differentiated germ cells and sexual maturity. NPYR-1 is expressed in neuroendocrine cells of the central nervous system and can be activated specifically by NPY-8 in cell-based assays. Additionally, we screened the complement of GPCRs with expression enriched in sexually reproducing planarians, and identified an orphan chemoreceptor family member, ophis, that controls differentiation of germline stem cells (GSCs). ophis is expressed in somatic cells of male and female gonads, as well as in accessory reproductive tissues. We have previously shown that somatic gonadal cells are required for male GSC specification and maintenance in planarians. However, ophis is not essential for GSC specification or maintenance and, therefore, defines a secondary role for planarian gonadal niche cells in promoting GSC differentiation. Our studies uncover the complement of planarian GPCRs and reveal previously unappreciated roles for these receptors in systemic and local (i.e., niche) regulation of germ cell development.
涡虫在生殖系维持方面表现出显著的可塑性,能够根据全身和环境线索发育或拆解生殖组织。在此,我们研究了G蛋白偶联受体(GPCRs)在这种动态生殖系调控中的作用。通过基于基因组的受体挖掘,我们鉴定出566个假定的涡虫GPCRs,并将它们分为保守和门特异性亚家族。我们进行了功能筛选,以确定NPYR-1是NPY-8的同源受体,NPY-8是性成熟和生殖细胞分化所需的一种神经肽。与NPY-8相似,该受体的敲低导致分化生殖细胞和性成熟的丧失。NPYR-1在中枢神经系统的神经内分泌细胞中表达,并且在基于细胞的试验中可以被NPY-8特异性激活。此外,我们筛选了在有性生殖涡虫中表达富集的GPCRs互补物,并鉴定出一个孤儿化学感受器家族成员ophis,它控制生殖系干细胞(GSCs)的分化。ophis在雄性和雌性性腺的体细胞以及附属生殖组织中表达。我们之前已经表明,体细胞性腺细胞是涡虫中雄性生殖系干细胞特化和维持所必需的。然而,ophis对于生殖系干细胞的特化或维持并非必不可少,因此,它定义了涡虫性腺微环境细胞在促进生殖系干细胞分化中的次要作用。我们的研究揭示了涡虫GPCRs的互补物,并揭示了这些受体在生殖细胞发育系统和局部(即微环境)调控中以前未被认识到的作用。