Siaussat David, Bozzolan Françoise, Porcheron Patrick, Debernard Stéphane
UMR 1272A Physiologie de l'Insecte, Signalisation et Communication, Université Pierre et Marie Curie, 7 quai Saint Bernard, 75005 Paris, France.
Insect Biochem Mol Biol. 2008 May;38(5):529-39. doi: 10.1016/j.ibmb.2008.01.001. Epub 2008 Jan 19.
The mechanisms involved in the control of cellular proliferation by the steroid hormone 20-hydroxyecdysone (20E) in insects are not known. We dissected the 20E signalling pathway responsible for G2/M arrest of imaginal cells from the IAL-PID2 cells of the Indian meal moth Plodia interpunctella. We first used a 5'-3' RACE-based strategy to clone a 4479bp cDNA encoding a putative P. interpunctella HR3 transcription factor named PiHR3. The deduced amino acid sequence of PiHR3 was highly similar to those of HR3 proteins from other lepidopterans, e.g. Manduca sexta and Bombyx mori. Using double-stranded RNA-mediated interference (dsRNAi), we then succeeded in blocking the ability of 20E to induce the expression of PiEcR-B1, PiUSP-2 and PiHR3 genes that encode the P. interpunctella ecdysone receptor B1-isoform, Ultraspiracle-2 isoform, the insect homologue of the vertebrate retinoid X receptor, and the HR3 transcription factor. We showed that inhibiting the 20E induction of PiEcR-B1, PiUSP-2 and PiHR3 mRNAs prevented the decreased expression of B cyclin and consequently the G2/M arrest of IAL-PID2 cells. Using this functional approach, we revealed the participation of EcR, USP and HR3 in a 20E signalling pathway that controls the proliferation of imaginal cells by regulating the expression of B cyclin.
昆虫中类固醇激素20-羟基蜕皮酮(20E)控制细胞增殖的机制尚不清楚。我们剖析了印度谷螟Plodia interpunctella的IAL-PID2细胞中负责imaginal细胞G2/M期阻滞的20E信号通路。我们首先采用基于5'-3' RACE的策略克隆了一个4479bp的cDNA,其编码一种推定的印度谷螟HR3转录因子,命名为PiHR3。PiHR3推导的氨基酸序列与其他鳞翅目昆虫(如烟草天蛾和家蚕)的HR3蛋白高度相似。然后,利用双链RNA介导的干扰(dsRNAi),我们成功地阻断了20E诱导PiEcR-B1、PiUSP-2和PiHR3基因表达的能力,这些基因分别编码印度谷螟蜕皮激素受体B1亚型、超气门蛋白-2亚型(脊椎动物类视黄醇X受体的昆虫同源物)和HR3转录因子。我们发现,抑制20E对PiEcR-B1、PiUSP-2和PiHR3 mRNA的诱导作用可防止B型细胞周期蛋白表达下降,从而防止IAL-PID2细胞的G2/M期阻滞。通过这种功能研究方法,我们揭示了EcR、USP和HR3参与了一条20E信号通路,该通路通过调节B型细胞周期蛋白的表达来控制imaginal细胞的增殖。