Department of Integrative Physiology and Center for Neuroscience, University of Colorado, Boulder, CO 80309-0354, USA.
Gen Comp Endocrinol. 2012 May 1;176(3):321-6. doi: 10.1016/j.ygcen.2011.11.030. Epub 2011 Dec 8.
Several protostomian molecules that structurally resemble chordate gonadotropin-releasing hormone (GnRH) have been identified through cloning, biochemical purification or data mining. These molecules share considerable sequence and structural similarities with chordate GnRH, leading to the current belief that protostomian and chordate forms of GnRH share a common ancestor. However, the physiological significance of these protostomian GnRH-like molecules remains poorly understood. This knowledge gap hampers our understanding of how GnRH has evolved functionally over time. This review provides a summary of our recent functional characterization of a GnRH-like molecule (ap-GnRH) in a gastropod mollusk, Aplysia californica, and presents preliminary proof for a cognate ap-GnRH receptor (ap-GnRHR). Our data reveal that ap-GnRH is a general neural regulator capable of exerting diverse central and motor effects, but plays little or no role in reproductive activation. This notion is supported by the abundance of a putative ap-GnRHR transcript in the central nervous system and the foot. Comparing these results to the available functional data from a cephalopod mollusk, Octopus vulgaris, we surmise that protostomian GnRH-like molecules are likely to assume a wide range of physiological roles, and reproductive activation is not an evolutionarily conserved role of these molecules. Future functional studies using suitable protostomian models are required to identify functional changes in protostomian GnRH-like molecules that accompany major taxa-level transitions.
已经通过克隆、生化纯化或数据挖掘鉴定出几种结构上类似于脊索动物促性腺激素释放激素(GnRH)的原口动物分子。这些分子与脊索动物 GnRH 具有相当大的序列和结构相似性,这导致目前人们相信原口动物和脊索动物形式的 GnRH 具有共同的祖先。然而,这些原口动物 GnRH 样分子的生理意义仍知之甚少。这一知识空白阻碍了我们对 GnRH 如何随时间在功能上进化的理解。本综述总结了我们最近对腹足纲软体动物 Aplysia californica 中一种 GnRH 样分子(ap-GnRH)的功能特征的研究,并初步证明了其同源的 ap-GnRH 受体(ap-GnRHR)的存在。我们的数据表明,ap-GnRH 是一种通用的神经调节剂,能够发挥多种中枢和运动效应,但在生殖激活中几乎没有作用或不起作用。这一观点得到了中枢神经系统和足部中大量假定的 ap-GnRHR 转录本的支持。将这些结果与来自头足类软体动物 Octopus vulgaris 的可用功能数据进行比较,我们推测原口动物 GnRH 样分子可能具有广泛的生理作用,而生殖激活并不是这些分子的一个进化保守作用。需要使用合适的原口动物模型进行未来的功能研究,以鉴定伴随主要分类群过渡的原口动物 GnRH 样分子的功能变化。