Related Experiment Video
Updated: May 26, 2026

The Drosophila Imaginal Disc Tumor Model: Visualization and Quantification of Gene Expression and Tumor Invasiveness Using Genetic Mosaics
Published on: October 6, 2016
The warts gene as a novel target of the Drosophila DRE/DREF transcription pathway
Abstract:
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.
Insights
The DRE/DREF pathway transcriptionally regulates the warts (wts) gene, a key component of the Hippo pathway. This study reveals a novel link between DRE/DREF and Hippo signaling in Drosophila development.
Area of Science:
- Cell Biology
- Genetics
- Developmental Biology
Background:
- The Hippo pathway regulates cell proliferation and apoptosis through core kinases like warts (wts).
- Transcriptional regulation of wts remains unclear.
- DREF transcription factor binds DRE sequences to control cell proliferation genes.
Purpose of the Study:
- Investigate the transcriptional regulation of the wts gene.
- Determine the role of the DRE/DREF pathway in Hippo signaling.
- Explore potential interactions between DRE/DREF and Hippo pathways in vivo.
Main Methods:
- Drosophila genetic interaction assays (wts gene dose reduction).
- Luciferase reporter assays to assess promoter activity.
- DREF-RNAi and knockdown experiments in S2 cells.
- Chromatin immunoprecipitation (ChIP) assays.
Main Results:
- Reduced wts gene dose enhanced DREF-induced rough eye phenotype, suggesting genetic interaction.
- DRE sequences in the wts promoter showed strong activity, reduced by DREF-RNAi.
- DREF knockdown decreased endogenous wts mRNA levels.
- DREF binds to the wts promoter in vivo.
Conclusions:
- The DRE/DREF pathway is essential for the transcriptional regulation of the wts gene.
- A novel link between the DRE/DREF and Hippo pathways is established.
- This interaction plays a role in Drosophila development.
More Related Videos
11:12Microinjection Wound Assay and In vivo Localization of Epidermal Wound Response Reporters in Drosophila Embryos.
Published on: November 1, 2013
07:23A Protocol for Genetic Induction and Visualization of Benign and Invasive Tumors in Cephalic Complexes of Drosophila melanogaster
Published on: September 11, 2013
Related Concept Videos
Canonical Wnt Signaling Pathway
Non-Canonical Wnt Signaling Pathways
Exon Recombination
Exon shuffling follows “splice frame rules.” Each exon has three reading...