Division of Biomolecular Research, Suntory Institute for Bioorganic Research, Osaka, Japan.
Mol Biol Evol. 2010 May;27(5):1097-106. doi: 10.1093/molbev/msp319. Epub 2009 Dec 21.
Gonadotropin-releasing hormones (GnRHs) play pivotal roles in control of reproduction via a hypothalamic-pituitary-periphery endocrine system and nervous systems of not only vertebrates but also invertebrates. GnRHs trigger several signal transduction cascades via GnRH receptors (GnRHRs), members of the G protein-coupled receptor (GPCR) family. Recently, six GnRHs (tunicate GnRH [tGnRH]-3 to tGnRH-8) and four GnRHRs (Ciona intestinalis [Ci]-GnRHR1 to GnRHR-4), including a species-specific paralog, Ci-GnRHR4 (R4) regarded as an orphan receptor or nonfunctional receptor, were identified in the protochordate, C. intestinalis, which lacks the hypothalamic-pituitary system. Here, we show novel functional modulation of GnRH signaling pathways via GPCR heterodimerization. Immunohistochemical analysis showed colocalization of R1 and R4 in test cells of the ascidian ovary. The native R1-R4 heterodimerization was detected in the Ciona ovary by coimmunoprecipitation analysis. The heterodimerization in HEK293 cells cotransfected with R1 and R4 was also observed by coimmunoprecipitation and fluorescent energy transfer analyses. Binding assay revealed that R4 had no affinity for tGnRHs, and the heterodimerization did not alter the binding affinity of R1 to the ligands. The R1-R4 elicited 10-fold more potent Ca2+ mobilization than R1 exclusively by tGnRH-6, although R1-mediated cyclic AMP production was not affected by any of tGnRHs via the R1-R4 heterodimer. Moreover, the R1-R4 heterodimer potentiated translocation of both Ca2+-dependent protein kinase C-alpha (PKCalpha) by tGnRH-6 and Ca2+-independent PKCzeta by tGnRH-5 and tGnRH-6, eventually leading to the upregulation of extracellular signal-regulated kinase (ERK) phosphorylation compared with R1 alone. These results provide evidence that the species-specific GnRHR orphan paralog, R4, serves as an endogenous modulator for the fine-tuning of activation of PKC subtype-selective signal transduction via heterodimerization with R1 and that the species-specific GPCR heterodimerization, in concert with multiplication of tGnRHs and Ci-GnRHRs, participates in functional evolution of neuropeptidergic GnRH signaling pathways highly conserved throughout the animal kingdom.
促性腺激素释放激素(GnRHs)通过下丘脑-垂体-外周内分泌系统和神经通路在脊椎动物和无脊椎动物的生殖控制中发挥关键作用。GnRHs 通过 GnRH 受体(GnRHRs)触发多种信号转导级联反应,GnRHRs 是 G 蛋白偶联受体(GPCR)家族的成员。最近,在无脊椎动物文昌鱼中鉴定出六种 GnRH(被囊动物 GnRH [tGnRH]-3 至 tGnRH-8)和四种 GnRHR(Ciona intestinalis [Ci]-GnRHR1 至 GnRHR-4),包括一种被认为是孤儿受体或非功能受体的物种特异性旁系同源物 Ci-GnRHR4(R4)。文昌鱼缺乏下丘脑-垂体系统。在这里,我们通过 GPCR 异二聚化显示 GnRH 信号通路的新的功能调节。免疫组织化学分析显示 R1 和 R4 在海鞘卵巢的测试细胞中存在共定位。通过共免疫沉淀分析检测到 Ci 卵巢中的天然 R1-R4 异二聚体。通过共免疫沉淀和荧光能量转移分析观察到在共转染 R1 和 R4 的 HEK293 细胞中也存在异二聚体。结合测定显示 R4 与 tGnRHs 没有亲和力,并且异二聚化不会改变 R1 与配体的结合亲和力。与 R1 单独相比,R1-R4 通过 tGnRH-6 引发 10 倍更强的 Ca2+动员,尽管 R1-R4 异二聚体通过任何一种 tGnRH 都不会影响 R1 介导的环 AMP 产生。此外,R1-R4 异二聚体增强了 tGnRH-6 诱导的 Ca2+-依赖性蛋白激酶 C-α(PKCalpha)和 tGnRH-5 和 tGnRH-6 诱导的 Ca2+-非依赖性 PKCzeta 的易位,最终导致与 R1 单独相比 ERK 磷酸化的上调。这些结果提供了证据表明,物种特异性 GnRHR 孤儿旁系同源物 R4 作为内源性调节剂,通过与 R1 形成异二聚体来精细调节 PKC 亚型选择性信号转导的激活,并且物种特异性 GPCR 异二聚体与 tGnRHs 和 Ci-GnRHRs 的增殖一起参与了神经肽 GnRH 信号通路的功能进化在整个动物王国中高度保守。