Am J Cancer Res. 2012;2(1):36-44. Epub 2011 Nov 22.
The Hippo tumor suppressor pathway in Drosophila represses expression of DIAP1 and Cyclin E via inactivation of the transcription co-activator Yorkie, resulting in cell cycle arrest and induction of apoptosis. The warts (wts) gene is well known as a core kinase in this pathway, but its transcriptional regulation has yet to be clarified. In Drosophila, DREF binds to a target sequence named DRE (5'-TATCGATA) and regulates transcription of cell proliferation-related genes containing the DRE sequence in their promoter regions. Here we found half reduction of the wts gene dose to enhance the DREF-induced rough eye phenotype, suggesting a DREF genetic interaction with the Hippo pathway in vivo. Three DREs indentified in the wts gene promoter region exhibited strong promoter activity with a luciferase transient expression assay in Drosophila S2 cells, this decreasing under DREF-RNAi conditions. In addition, knockdown of DREF in S2 cells reduced the level of endogenous wts mRNA. Chromatin immunoprecipitation assays with anti-DREF antibody revealed that DREF binds specifically to the wts gene promoter region containing DREs in vivo. These results indicate that the DRE/DREF pathway is required for transcriptional regulation of the wts gene, indicating a novel link between the DRE/DREF and the Hippo pathways.
果蝇中的 Hippo 肿瘤抑制途径通过失活转录共激活因子 Yorkie 来抑制 DIAP1 和 Cyclin E 的表达,从而导致细胞周期停滞和凋亡诱导。warts(wts)基因是该途径中的核心激酶,但它的转录调控尚未阐明。在果蝇中,DREF 结合到一个名为 DRE(5'-TATCGATA)的靶序列,并调节含有 DRE 序列的细胞增殖相关基因的转录,这些基因在其启动子区域。在这里,我们发现 wts 基因剂量减少一半可增强 DREF 诱导的粗糙眼表型,表明 DREF 在体内与 Hippo 途径存在遗传相互作用。在果蝇 S2 细胞中,用荧光素酶瞬时表达试验在 wts 基因启动子区域鉴定出的三个 DREs 显示出很强的启动子活性,在 DREF-RNAi 条件下,其活性降低。此外,S2 细胞中 DREF 的敲低降低了内源性 wts mRNA 的水平。用抗 DREF 抗体进行的染色质免疫沉淀试验表明,DREF 在体内特异性结合含有 DRE 的 wts 基因启动子区域。这些结果表明,DRE/DREF 途径是 wts 基因转录调控所必需的,这表明 DRE/DREF 和 Hippo 途径之间存在新的联系。