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首页> 外文期刊>The Journal of Experimental Biology >Search for hepatopancreatic ecdysteroid-responsive genes during the crayfish molt cycle: from a single gene to multigenicity
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Search for hepatopancreatic ecdysteroid-responsive genes during the crayfish molt cycle: from a single gene to multigenicity

机译:在小龙虾蜕皮周期中寻找肝胰腺蜕皮激素反应性基因:从单个基因到多基因

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The expression of the vitellogenin gene of the red-claw crayfish Cherax quadricarinatus (CqVg) was previously demonstrated in male crayfish during an endocrinologically induced molt cycle. The hypothesis that this expression is under the direct control of ecdysteroids was tested in this study both in vivo and in vitro. Unlike vitellogenin of insects, CqVg was not found to be ecdysteroid-responsive. Thus, a multigenic approach was employed for the identification of other hepatopancreatic ecdysteroid-responsive genes by a cDNA microarray. For the purposes of this study, a multi-parametric molt-staging technique, based on X-ray detection of gastrolith growth, was developed. To identify ecdysteroid-responsive genes during premolt, the molt cycle was induced by two manipulations, 20-hydroxyecdysone administration and X-organ-sinus gland complex removal; both resulted in significant elevation of ecdysteroids. Two clusters of affected genes (129 and 122 genes, respectively) were revealed by the microarray. It is suggested that only genes belonging to similarly responsive (up- or downregulated) gene clusters in both manipulations (102 genes) could be considered putative ecdysteroid-responsive genes. Some of these ecdysteroid-responsive genes showed homology to genes controlling chitin metabolism, proteases and other cellular activities, while 56.8% were unknown. The majority of the genes were downregulated, presumably by an energetic shift of the hepatopancreas prior to ecdysis. The effect of 20-hydroxyecdysone on representative genes from this group was confirmed in vitro using a hepatopancreas tissue culture. This approach for ecdysteroid-responsive gene identification could also be implemented in other tissues for the elucidation of ecdysteroid-specific signaling pathways during the crustacean molt cycle.
机译:红爪小龙虾Cherax quadricarinatus(CqVg)的卵黄蛋白生成素基因的表达先前已在内分泌诱导的蜕皮周期中在雄性小龙虾中得到证实。在体内和体外的这项研究中都检验了这种表达受蜕皮类固醇直接控制的假说。与昆虫卵黄蛋白生成素不同,未发现CqVg对蜕皮激素反应敏感。因此,采用多基因方法通过cDNA微阵列鉴定其他肝胰腺蜕皮激素反应性基因。为了本研究的目的,开发了一种基于X射线检测胃石生长的多参数蜕皮分期技术。为了鉴定蜕皮过程中蜕皮甾类的响应基因,通过两种操作诱导蜕皮周期:20-羟基蜕皮激素的施用和X-器官-窦腺复合体的去除。两者都导致蜕皮甾类的显着升高。微阵列揭示了两个受影响的基因簇(分别为129和122个基因)。建议在两种操作中只有属于类似响应(上调或下调)基因簇的基因(102个基因)才可以被认为是蜕皮甾类响应基因。这些蜕皮类固醇反应性基因中的某些与控制甲壳质代谢,蛋白酶和其他细胞活性的基因显示出同源性,而未知的占56.8%。大多数基因被下调,大概是在蜕皮之前肝胰腺的能量转移。使用肝胰腺组织培养在体外证实了20-羟基蜕皮激素对该组代表性基因的作用。蜕皮激素反应性基因鉴定的这种方法也可以在其他组织中实施,以阐明甲壳动物蜕皮周期中的蜕皮激素特异性信号传导途径。

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