Siaussat David, Bozzolan Françoise, Queguiner Isabelle, Porcheron Patrick, Debernard Stéphane
Laboratoire de Physiologie Cellulaire des Invertébrés, Université Pierre et Marie Curie, Paris, France.
Eur J Biochem. 2004 Jul;271(14):3017-27. doi: 10.1111/j.1432-1033.2004.04233.x.
The IAL-PID2 cells derived from imaginal wing discs of the last larval instar of Plodia interpunctella were responsive to 20-hydroxyecdysone (20E). These imaginal cells respond to 20E by proliferative arrest followed by a morphological differentiation. These 20E-induced late responses were inhibited in presence of juvenile hormone (JH II). From these imaginal wing cells, we have cloned a cDNA sequence encoding a P. interpunctella ecdysone receptor-B1 isoform (PIEcR-B1). The amino acid sequence of PIEcR-B1 showed a high degree of identity with EcR-B1 isoforms of Bombyx mori, Manduca sexta and Choristoneura fumiferana. The pattern of PIEcR-B1mRNA induction by 20E was characterized by a biphasic response with peaks at 2 h and 18 h. The presence of the protein synthesis inhibitor anisomycin induced a slight reduction in level of PIEcR-B1 mRNA and prevented the subsequent declines observed in 20E-treated cells. Therefore, PIEcR-B1 mRNA was directly induced by 20E and its downregulation depended on protein synthesis. An exposure of imaginal wing cells to 20E in the presence of JH II caused an increased expression of Plodia E75-B and HR3 transcription factors but inhibited the second increase of PIEcR-B1 mRNA. These findings showed that in vitro JH II was able to prevent the 20E-induced differentiation of imaginal wing cells. This effect could result from a JH II action on the 20E-induced genetic cascade through a modulation of EcR-B1, E75-B and HR3 expression.
来源于印度谷螟末龄幼虫翅芽的IAL-PID2细胞对20-羟基蜕皮酮(20E)有反应。这些成虫细胞对20E的反应先是增殖停滞,随后发生形态分化。在保幼激素(JH II)存在的情况下,这些20E诱导的晚期反应受到抑制。从这些成虫翅细胞中,我们克隆了一个编码印度谷螟蜕皮激素受体-B1亚型(PIEcR-B1)的cDNA序列。PIEcR-B1的氨基酸序列与家蚕、烟草天蛾和云杉色卷蛾的EcR-B1亚型高度同源。20E诱导PIEcR-B1mRNA的模式表现为双相反应,在2小时和18小时出现峰值。蛋白质合成抑制剂茴香霉素的存在导致PIEcR-B1mRNA水平略有降低,并阻止了在20E处理细胞中观察到的随后下降。因此,PIEcR-B1mRNA是由20E直接诱导的,其下调依赖于蛋白质合成。在JH II存在的情况下,将成虫翅细胞暴露于20E会导致印度谷螟E75-B和HR3转录因子的表达增加,但会抑制PIEcR-B1mRNA的第二次增加。这些发现表明,在体外JH II能够阻止20E诱导的成虫翅细胞分化。这种作用可能是由于JH II通过调节EcR-B1、E75-B和HR3的表达对20E诱导的基因级联反应产生作用。