Xie Xi, Zhou Yanqi, Liu Mingxin, Tao Tian, Jiang Qinghua, Zhu Dongfa
School of Marine Science, Ningbo University, 315211 Ningbo, China.
School of Marine Science, Ningbo University, 315211 Ningbo, China.
Comp Biochem Physiol B Biochem Mol Biol. 2016 Oct;200:69-77. doi: 10.1016/j.cbpb.2016.06.004. Epub 2016 Jun 15.
The nuclear receptor E75 is an early-responsive gene in 20-hydroxyecdysone (20E) signaling pathway, and is found to play essential roles in many aspects of arthropods development. In this study, a cDNA encoding the E75 nuclear receptor of the swimming crab, Portunus trituberculatus was cloned using RT-PCR and RACE. The PtE75 cDNA was 3211bp in length, and encodes a protein of 795 amino acids. The DBD region of the predicted amino acid sequence for PtE75 was highly conserved with other arthropoda E75s, while its LBD region was more similar to decapod E75s. Tissue distribution analysis showed that PtE75 transcript was widespread among tissues and relatively abundant in Y-organ, epidermis, eyestalk, and muscles. PtE75 exhibited tissue-specific expression patterns in these four tissues, which may depend on the distinct action of 20E on different tissues. The expression of PtE75 in Y-organ and epidermis were induced by eyestalk ablation (ESA), indicating its responsiveness to the increasing hemolymph 20E titer. To identify potential targets for ecdysteroid control the in Y-organ, epidermis, and eyestalk, the expression change of an ecdysteroid synthesis gene PtSad in Y-organ, a chitin degradation gene PtChi1 in epidermis, and the molt-inhibiting hormone gene PtMIH in eyestalk were investigated after silencing of PtE75 mRNA. The double stranded RNA (dsRNA) of PtE75 caused a loss in PtChi and PtMIH expression, while an increase in PtSad expression. The results suggested that the ecdysteroids may act through E75, and play a stimulatory role on chitin degradation in epidermis and MIH synthesis in eyestalk, and an negative feedback effect on ecdysteroid synthesis in Y-organ.
核受体E75是20-羟基蜕皮激素(20E)信号通路中的一个早期反应基因,并且发现在节肢动物发育的许多方面发挥着重要作用。在本研究中,利用RT-PCR和RACE技术克隆了三疣梭子蟹核受体E75的cDNA。三疣梭子蟹E75 cDNA长度为3211bp,编码一个795个氨基酸的蛋白质。预测的三疣梭子蟹E75氨基酸序列的DBD区域与其他节肢动物的E75高度保守,而其LBD区域与十足目E75更相似。组织分布分析表明,三疣梭子蟹E75转录本在各组织中广泛存在,在Y器官、表皮、眼柄和肌肉中相对丰富。三疣梭子蟹E75在这四种组织中表现出组织特异性表达模式,这可能取决于20E对不同组织的不同作用。眼柄切除(ESA)诱导了三疣梭子蟹E75在Y器官和表皮中的表达,表明其对血淋巴中20E滴度升高的反应。为了确定Y器官、表皮和眼柄中蜕皮类固醇控制的潜在靶点,在沉默三疣梭子蟹E75 mRNA后,研究了Y器官中蜕皮类固醇合成基因三疣梭子蟹Sad、表皮中几丁质降解基因三疣梭子蟹Chi1和眼柄中蜕皮抑制激素基因三疣梭子蟹MIH的表达变化。三疣梭子蟹E75的双链RNA(dsRNA)导致三疣梭子蟹Chi和三疣梭子蟹MIH表达缺失,而三疣梭子蟹Sad表达增加。结果表明,蜕皮类固醇可能通过E75发挥作用,对表皮中的几丁质降解和眼柄中的MIH合成起刺激作用,对Y器官中的蜕皮类固醇合成起负反馈作用。