Nakagawa Yoshiaki, Henrich Vincent C
Division of Applied Sciences, Graduate School of Agriculture, Kyoto University, Kitashirakawa, Sakyo-Ku, Kyoto 606-8502, Japan.
FEBS J. 2009 Nov;276(21):6128-57. doi: 10.1111/j.1742-4658.2009.07347.x. Epub 2009 Sep 30.
The molting process in arthropods is regulated by steroid hormones acting via nuclear receptor proteins. The most common molting hormone is the ecdysteroid, 20-hydroxyecdysone. The receptors of 20-hydroxyecdysone have also been identified in many arthropod species, and the amino acid sequences determined. The functional molting hormone receptors consist of two members of the nuclear receptor superfamily, namely the ecdysone receptor and the ultraspiracle, although the ecdysone receptor may be functional, in some instances, without the ultraspiracle. Generally, the ecdysone receptor/ultraspiracle heterodimer binds to a number of ecdysone response elements, sequence motifs that reside in the promoter of various ecdysteroid-responsive genes. In the ensuing transcriptional induction, the ecdysone receptor/ultraspiracle complex binds to 20-hydroxyecdysone or to a cognate ligand that, in turn, leads to the release of a corepressor and the recruitment of coactivators. 3D structures of the ligand-binding domains of the ecdysone receptor and the ultraspiracle have been solved for a few insect species. Ecdysone agonists bind to ecdysone receptors specifically, and ligand-ecdysone receptor binding is enhanced in the presence of the ultraspiracle in insects. The basic mode of ecdysteroid receptor action is highly conserved, but substantial functional differences exist among the receptors of individual species. Even though the transcriptional effects are apparently similar for ecdysteroids and nonsteroidal compounds such as diacylhydrazines, the binding shapes are different between them. The compounds having the strongest binding affinity to receptors ordinarily have strong molting hormone activity. The ability of the ecdysone receptor/ultraspiracle complex to manifest the effects of small lipophilic agonists has led to their use as gene switches for medical and agricultural applications.
节肢动物的蜕皮过程由通过核受体蛋白起作用的类固醇激素调节。最常见的蜕皮激素是蜕皮甾酮,即20-羟基蜕皮酮。在许多节肢动物物种中也已鉴定出20-羟基蜕皮酮的受体,并确定了其氨基酸序列。功能性蜕皮激素受体由核受体超家族的两个成员组成,即蜕皮激素受体和超气门蛋白,不过在某些情况下,蜕皮激素受体在没有超气门蛋白的情况下也可能发挥功能。一般来说,蜕皮激素受体/超气门蛋白异二聚体与多个蜕皮激素反应元件结合,这些序列基序存在于各种蜕皮甾酮反应基因的启动子中。在随后的转录诱导过程中,蜕皮激素受体/超气门蛋白复合物与20-羟基蜕皮酮或同源配体结合,进而导致共抑制因子的释放和共激活因子的募集。已经解析了几种昆虫物种的蜕皮激素受体和超气门蛋白的配体结合结构域的三维结构。蜕皮激素激动剂特异性地与蜕皮激素受体结合,在昆虫中,超气门蛋白的存在会增强配体与蜕皮激素受体的结合。蜕皮甾酮受体作用的基本模式高度保守,但各个物种的受体之间存在显著的功能差异。尽管蜕皮甾酮和非甾体化合物(如双酰肼)的转录效应明显相似,但它们之间的结合形式不同。通常,与受体具有最强结合亲和力的化合物具有很强的蜕皮激素活性。蜕皮激素受体/超气门蛋白复合物表现出小亲脂性激动剂效应的能力,使其被用作医学和农业应用中的基因开关。