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蜕皮激素受体B1(EcR-B1)和超气门蛋白(Usp)核激素受体在果蝇卵子发生过程中调节VM32E卵壳基因的表达。

EcR-B1 and Usp nuclear hormone receptors regulate expression of the VM32E eggshell gene during Drosophila oogenesis.

作者信息

Bernardi Fabio, Romani Patrizia, Tzertzinis George, Gargiulo Giuseppe, Cavaliere Valeria

机构信息

Dipartimento di Biologia Evoluzionistica Sperimentale, Università di Bologna, Bologna, Italy.

出版信息

Dev Biol. 2009 Apr 15;328(2):541-51. doi: 10.1016/j.ydbio.2009.01.013. Epub 2009 Jan 20.

Abstract

Ecdysone signaling plays key roles in Drosophila oogenesis, as its activity is required at multiple steps during egg chamber maturation. Recently, its involvement has been reported on eggshell production by controlling chorion gene transcription and amplification. Here, we present evidence that ecdysone signaling also controls the expression of the eggshell gene VM32E, whose product is a component of vitelline membrane and endochorion layers. Specifically blocking the function of the different Ecdysone receptor (EcR) isoforms we demonstrate that EcR-B1 is responsible for ecdysone-mediated VM32E transcriptional regulation. Moreover, we show that the EcR partner Ultraspiracle (Usp) is also necessary for VM32E expression. By analyzing the activity of specific VM32E regulatory regions in usp(2) clones we identify the promoter region mediating ecdysone-dependent VM32E expression. By in vitro binding assay and site-directed mutagenesis we demonstrate that this region contains a Usp binding site necessary for VM32E regulation. Our results further support the crucial role of ecdysone signaling in controlling transcription of eggshell structural genes and suggest that the heterodimeric complex EcR-B1/Usp mediates the ecdysone-dependent VM32E transcriptional activation in the main body follicle cells.

摘要

蜕皮激素信号传导在果蝇卵子发生过程中发挥关键作用,因为在卵室成熟的多个步骤中都需要其活性。最近,有报道称它通过控制绒毛膜基因的转录和扩增参与卵壳的产生。在此,我们提供证据表明,蜕皮激素信号传导还控制卵壳基因VM32E的表达,其产物是卵黄膜和内卵壳层的一个组成部分。通过特异性阻断不同蜕皮激素受体(EcR)亚型的功能,我们证明EcR-B1负责蜕皮激素介导的VM32E转录调控。此外,我们表明EcR的伙伴超气门蛋白(Usp)对于VM32E的表达也是必需的。通过分析usp(2)克隆中特定VM32E调控区域的活性,我们确定了介导蜕皮激素依赖性VM32E表达的启动子区域。通过体外结合试验和定点诱变,我们证明该区域包含一个对VM32E调控必需的Usp结合位点。我们的结果进一步支持了蜕皮激素信号传导在控制卵壳结构基因转录中的关键作用,并表明异二聚体复合物EcR-B1/Usp在主体卵泡细胞中介导蜕皮激素依赖性VM32E的转录激活。

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