Genetic Modifier Screens on Hairless Gain-of-Function Phenotypes Reveal Genes Involved in Cell Differentiation, Cell Growth and Apoptosis in Drosophila melanogaster
Genetic Modifier Screens on Hairless Gain-of-Function Phenotypes Reveal Genes Involved in Cell Differentiation, Cell Growth and Apoptosis in Drosophila melanogaster
Abstract Overexpression of Hairless (H) causes a remarkable degree of tissue loss and apoptosis during imaginal development. H functions as antagonist in the Notch-signaling pathway in Drosophila, and the link to growth and apoptosis is poorly understood. To further our insight into H-mediated apoptosis, we performed two large-scale screens for modifiers of a small rough eye phenotype caused by H overexpression. Both loss- and gain-of-function screens revealed known and new genetic interactors representing diverse cellular functions. Many of them did not cause eye phenotypes on their own, emphasizing a specific genetic interaction with H. As expected, we also identified components of different signaling pathways supposed to be involved in the regulation of cell growth and cell death. Accordingly, some of them also acted as modifiers of proapoptotic genes, suggesting a more general involvement in the regulation of apoptosis. Overall, these screens highlight the importance of H and the Notch pathway in mediating cell death in response to developmental and environmental cues and emphasize their role in maintaining developmental cellular homeostasis.
- University of Hohenheim Germany
Male, JNK Mitogen-Activated Protein Kinases, Apoptosis, Cell Differentiation, Cell Enlargement, Inhibitor of Apoptosis Proteins, ErbB Receptors, Drosophila melanogaster, Animals, Drosophila Proteins, Female, Eye Abnormalities, Receptors, Invertebrate Peptide, Protein Kinases, Signal Transduction, Transcription Factors
Male, JNK Mitogen-Activated Protein Kinases, Apoptosis, Cell Differentiation, Cell Enlargement, Inhibitor of Apoptosis Proteins, ErbB Receptors, Drosophila melanogaster, Animals, Drosophila Proteins, Female, Eye Abnormalities, Receptors, Invertebrate Peptide, Protein Kinases, Signal Transduction, Transcription Factors
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