Ren Qian-Qian, Long Gui-Yun, Yang Hong, Zhou Cao, Yang Xi-Bin, Yan Yi, Yan Xin
Provincial Key Laboratory for Agricultural Pest Management of Mountainous Region, Institute of Entomology, Guizhou University, Guiyang, China.
School of Chinese Ethnic Medicine, Key Laboratory of Guizhou Ethnic Medicine Resource Development and Utilization in Guizhou Minzu, Guizhou Minzu University, Guiyang, 550025, China.
J Econ Entomol. 2024 Aug 12;117(4):1675-1685. doi: 10.1093/jee/toae123.
Molting is a key solution to growth restriction in insects. The periodic synthesis and degradation of chitin, one of the major components of the insect epidermis, is necessary for insect growth. MicroRNA (miRNA) have been implicated in molting regulation, yet their involvement in the interplay interaction between the chitin synthesis pathway and 20-hydroxyecdysone signaling remains poorly understood. In this study, soluble trehalase (Tre1) and phosphoacetylglucosamine mutase (PAGM) were identified as targets of conserved miR-8-3p and miR-2a-3, respectively. The expression profiles of miR-8-3p-SfTre1 and miR-2a-3-SfPAGM exhibited an opposite pattern during the different developmental stages, indicating a negative regulatory relationship between them. This relationship was confirmed by an in vitro dual-luciferase reporter system. Overexpression of miR-8-3p and miR-2a-3 by injection of mimics inhibited the expression of their respective target genes and increased mortality, leading to death in the pre-molting, and molting death phenomena. They also caused a decrease in chitin content and expression levels of key genes in the chitin synthesis pathway (SfTre1, SfTre2, SfHK, SfG6PI, SfGFAT, SfGNA, SfPAGM, SfUAP, SfCHS1, SfCHS1a, and SfCHS1b). Conversely, the injection of miRNA inhibitors resulted in the upregulation of the expression levels of these genes. Following 20E treatment, the expression levels of miR-8-3p and miR-2a-3 decreased significantly, while their corresponding target genes increased significantly. These results indicate that miR-8-3p and miR-2a-3 play a regulatory role in the molting of Sogatella furcifera by targeting SfTre1 and SfPAGM, respectively. These findings provide new potential targets for the development of subsequent new control strategies.
蜕皮是昆虫应对生长限制的关键方式。几丁质是昆虫表皮的主要成分之一,其周期性的合成与降解对昆虫生长至关重要。微小RNA(miRNA)已被证明参与蜕皮调控,但其在几丁质合成途径与20-羟基蜕皮酮信号之间的相互作用中的作用仍知之甚少。在本研究中,可溶性海藻糖酶(Tre1)和磷酸乙酰葡糖胺变位酶(PAGM)分别被鉴定为保守miR-8-3p和miR-2a-3的靶标。miR-8-3p-SfTre1和miR-2a-3-SfPAGM的表达谱在不同发育阶段呈现相反模式,表明它们之间存在负调控关系。体外双荧光素酶报告系统证实了这种关系。通过注射模拟物过表达miR-8-3p和miR-2a-3可抑制其各自靶基因的表达并增加死亡率,导致在蜕皮前死亡以及蜕皮死亡现象。它们还导致几丁质含量以及几丁质合成途径中关键基因(SfTre1、SfTre2、SfHK、SfG6PI、SfGFAT、SfGNA、SfPAGM、SfUAP、SfCHS1、SfCHS1a和SfCHS1b)的表达水平降低。相反,注射miRNA抑制剂导致这些基因的表达水平上调。经20E处理后,miR-8-3p和miR-2a-3的表达水平显著降低,而其相应靶基因显著增加。这些结果表明,miR-8-3p和miR-2a-3分别通过靶向SfTre1和SfPAGM在褐飞虱蜕皮过程中发挥调控作用。这些发现为后续新型防治策略的开发提供了新的潜在靶点。