Siaussat D, Bozzolan F, Porcheron P, Debernard S
UMR 1272 Physiologie de l'Insecte, Signalisation et Communication, Université Pierre et Marie Curie, 12 rue Cuvier, 75005 Paris, France.
Cell Mol Life Sci. 2007 Feb;64(3):365-76. doi: 10.1007/s00018-007-6452-0.
To dissect the steroid hormone signaling pathway involved in insect cell morphological differentiation, we extended the application of the double-stranded RNA-mediated interference (dsRNAi) method to the epidermal IAL-PID2 cell line from Plodia interpunctella Lepidoptera. We first demonstrated that dsRNA was capable of efficiently blocking the steroid hormone 20-hydroxyecdysone (20E) inducibility of proteins that belong to the nuclear receptor superfamily, including the ecdysone receptor (EcR), its partner Ultraspiracle (USP), the insect homolog of the vertebrate retinoid X receptor and the HR3 transcription factor. We then showed that inhibiting the 20E induction of EcR, USP or HR3 proteins prevented the increased synthesis of beta tubulin and consequently the morphological transformation of cells. Thanks to this functional approach, we have shown, for the first time, the participation of EcR, USP and HR3 in a 20E signaling pathway that directs morphological differentiation in insect cells by regulating beta tubulin expression.
为剖析参与昆虫细胞形态分化的类固醇激素信号通路,我们将双链RNA介导的干扰(dsRNAi)方法的应用扩展至鳞翅目昆虫印度谷螟的表皮IAL-PID2细胞系。我们首先证明,dsRNA能够有效阻断类固醇激素20-羟基蜕皮激素(20E)对属于核受体超家族的蛋白质的诱导作用,这些蛋白质包括蜕皮激素受体(EcR)、其伴侣超气门蛋白(USP)、脊椎动物类视黄醇X受体的昆虫同源物以及HR3转录因子。然后我们表明,抑制EcR、USP或HR3蛋白的20E诱导作用可阻止β微管蛋白合成增加,从而防止细胞发生形态转变。借助这种功能研究方法,我们首次证明了EcR、USP和HR3参与了一条20E信号通路,该通路通过调节β微管蛋白表达来指导昆虫细胞的形态分化。