Cai Mei-Juan, Liu Wen, Pei Xu-Yang, Li Xiang-Ru, He Hong-Juan, Wang Jin-Xing, Zhao Xiao-Fan
Key Laboratory of Plant Cell Engineering and Germplasm Innovation of Ministry of Education / Shandong Provincial Key Laboratory of Animal Cells and Developmental Biology, School of Life Sciences, Shandong University, Jinan, Shandong 250100, China.
Key Laboratory of Plant Cell Engineering and Germplasm Innovation of Ministry of Education / Shandong Provincial Key Laboratory of Animal Cells and Developmental Biology, School of Life Sciences, Shandong University, Jinan, Shandong 250100, China.
J Biol Chem. 2014 Sep 19;289(38):26630-26641. doi: 10.1074/jbc.M114.581876. Epub 2014 Aug 5.
The steroid hormone 20-hydroxyecdysone (20E) initiates insect molting and metamorphosis. By contrast, juvenile hormone (JH) prevents metamorphosis. However, the mechanism by which JH inhibits metamorphosis remains unclear. In this study, we propose that JH induces the phosphorylation of Broad isoform Z7 (BrZ7), a newly identified protein, to inhibit 20E-mediated metamorphosis in the lepidopteran insect Helicoverpa armigera. The knockdown of BrZ7 in larvae inhibited metamorphosis by repressing the expression of the 20E response gene. BrZ7 was weakly expressed and phosphorylated during larval growth but highly expressed and non-phosphorylated during metamorphosis. JH regulated the rapid phosphorylation of BrZ7 via a G-protein-coupled receptor-, phospholipase C-, and protein kinase C-triggered pathway. The phosphorylated BrZ7 bound to the 5'-regulatory region of calponin to regulate its expression in the JH pathway. Exogenous JH induced BrZ7 phosphorylation to prevent metamorphosis by suppressing 20E-related gene transcription. JH promoted non-phosphorylated calponin interacting with ultraspiracle protein to activate the JH pathway and antagonize the 20E pathway. This study reveals one of the possible mechanisms by which JH counteracts 20E-regulated metamorphosis by inducing the phosphorylation of BrZ7.
类固醇激素20-羟基蜕皮酮(20E)启动昆虫的蜕皮和变态。相比之下,保幼激素(JH)则阻止变态。然而,JH抑制变态的机制仍不清楚。在本研究中,我们提出JH诱导一种新鉴定的蛋白质Broad异构体Z7(BrZ7)磷酸化,以抑制鳞翅目昆虫棉铃虫中20E介导的变态。敲低幼虫体内的BrZ7可通过抑制20E反应基因的表达来抑制变态。BrZ7在幼虫生长期间表达较弱且处于磷酸化状态,但在变态期间高度表达且未磷酸化。JH通过G蛋白偶联受体、磷脂酶C和蛋白激酶C触发的途径调节BrZ7的快速磷酸化。磷酸化的BrZ7与钙调蛋白的5'-调控区域结合,以调节其在JH途径中的表达。外源性JH诱导BrZ7磷酸化,通过抑制20E相关基因转录来阻止变态。JH促进非磷酸化的钙调蛋白与超气门蛋白相互作用,以激活JH途径并拮抗20E途径。本研究揭示了JH通过诱导BrZ7磷酸化来对抗20E调控的变态的一种可能机制。