Graduate School of Bio-Application and Systems Engineering, Tokyo University of Agriculture and Technology, Naka 2-24-16, Koganei 184-8588, Tokyo, Japan.
Int J Mol Sci. 2024 Sep 21;25(18):10157. doi: 10.3390/ijms251810157.
Complete elucidation of members of the gustatory receptor (Gr) family in lepidopteran insects began in the silkworm . Grs of lepidopteran insects were initially classified into four subfamilies based on the results of phylogenetic studies and analyses of a few ligands. However, with further ligand analysis, it has become clear that plant secondary metabolites are important targets not only for Grs in the bitter subfamily but also for the Gr43a orthologue subfamily and Grs in the sugar subfamily. Gene knockout experiments showed that Gr6 (BmGr6) and BmGr9 are involved in the recognition of the feeding-promoting compounds chlorogenic acid and isoquercetin in mulberry leaves by the maxillary palps, suggesting that these Grs are responsible for palpation-dependent host recognition without biting. On the other hand, BmGr expression was also confirmed in nonsensory organs. Midgut enteroendocrine cells that produce specific neuropeptides were shown to express specific BmGrs, suggesting that BmGrs are involved in the induction of endocrine secretion in response to changes in the midgut contents. Furthermore, gene knockout experiments indicated that BmGr6 is indeed involved in the secretion of myosuppressin. On the other hand, BmGr9 was shown to induce signal transduction that is not derived from the intracellular signaling cascade mediated by G proteins but from the fructose-regulated cation channel of BmGr9 itself. Cryogenic electron microscopy revealed the mechanism by which the ion channel of the BmGr9 homotetramer opens upon binding of fructose to the ligand-binding pocket. Research on BmGrs has contributed greatly to our understanding of the functions and roles of Grs in insects.
昆虫味觉受体(Gr)家族成员的全面阐述始于家蚕。根据系统发育研究和少数配体分析的结果,最初将鳞翅目昆虫的 Grs 分为四个亚科。然而,随着进一步的配体分析,很明显植物次生代谢物不仅是苦味亚科的 Grs,也是 Gr43a 同源亚科和糖亚科的 Grs 的重要靶标。基因敲除实验表明,Gr6(BmGr6)和 BmGr9 参与了下颚对桑叶中促食化合物绿原酸和异槲皮苷的识别,这表明这些 Grs 负责无需咀嚼的触须依赖性宿主识别。另一方面,BmGr 的表达也在非感觉器官中得到证实。产生特定神经肽的中肠肠内分泌细胞被证明表达特定的 BmGrs,这表明 BmGrs 参与了对中肠内容物变化的内分泌分泌的诱导。此外,基因敲除实验表明,BmGr6 确实参与了肌抑制素的分泌。另一方面,BmGr9 诱导的信号转导并非来自 G 蛋白介导的细胞内信号级联,而是来自 BmGr9 自身的果糖调节阳离子通道。低温电子显微镜揭示了 BmGr9 同源四聚体的离子通道在与配体结合口袋结合果糖时打开的机制。对 BmGrs 的研究极大地促进了我们对昆虫中 Grs 的功能和作用的理解。