Suppr超能文献

蜕皮激素诱导的锌指转录因子Crol调节果蝇中的Wg转录和细胞周期进程。

The Ecdysone-inducible zinc-finger transcription factor Crol regulates Wg transcription and cell cycle progression in Drosophila.

作者信息

Mitchell Naomi, Cranna Nicola, Richardson Helena, Quinn Leonie

机构信息

Department of Anatomy and Cell Biology, University of Melbourne, Parkville 3010, Melbourne, Australia.

出版信息

Development. 2008 Aug;135(16):2707-16. doi: 10.1242/dev.021766. Epub 2008 Jul 9.

Abstract

The steroid hormone Ecdysone is crucial for developmental cell death, proliferation and morphogenesis in Drosophila. Herein, we delineate a molecular pathway linking Ecdysone signalling to cell cycle regulation in the Drosophila developing wing. We present evidence that the Ecdysone-inducible zinc-finger transcription factor Crol provides a crucial link between the Ecdysone steroid hormone pathway and the Wingless (Wg) signalling pathway in Drosophila. We identified Crol as a strong enhancer of a wing phenotype generated by overexpression of the Wg-inducible cell cycle inhibitor Hfp. We demonstrate that Crol is required for cell cycle progression: crol mutant clones have reduced cell cycles and are removed by apoptosis, while upregulation of Crol overrides the Wg-mediated developmental cell cycle arrest in the zone of non-proliferating cells in the wing disc. Furthermore, we show that Crol acts to repress wg transcription. We also show that overexpression of crol results in downregulation of Hfp, consistent with the identification of the crol mutant as a dominant enhancer of the Hfp overexpression phenotype. Taken together, our studies have revealed a novel mechanism for cell cycle regulation, whereby Crol links steroid hormone signals to Wg signalling and the regulation of crucial cell cycle targets.

摘要

类固醇激素蜕皮激素对于果蝇发育过程中的细胞死亡、增殖和形态发生至关重要。在此,我们描绘了一条将蜕皮激素信号与果蝇发育翅膀中的细胞周期调控联系起来的分子途径。我们提供证据表明,蜕皮激素诱导型锌指转录因子Crol在果蝇的蜕皮激素类固醇激素途径与无翅(Wg)信号途径之间提供了关键联系。我们将Crol鉴定为Wg诱导型细胞周期抑制剂Hfp过表达所产生的翅膀表型的强力增强子。我们证明Crol是细胞周期进展所必需的:crol突变克隆的细胞周期缩短,并通过凋亡被清除,而Crol的上调则克服了Wg介导的翅膀圆盘非增殖细胞区的发育性细胞周期停滞。此外,我们表明Crol起到抑制wg转录的作用。我们还表明,crol的过表达导致Hfp下调,这与将crol突变体鉴定为Hfp过表达表型的显性增强子一致。综上所述,我们的研究揭示了一种新的细胞周期调控机制,即Crol将类固醇激素信号与Wg信号以及关键细胞周期靶点的调控联系起来。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验