Rhomboid 3 orchestrates Slit-independent repulsion of tracheal branches at the CNS midline
doi: 10.1242/dev.01242
pmid: 15229181
Rhomboid 3 orchestrates Slit-independent repulsion of tracheal branches at the CNS midline
EGF-receptor ligands act as chemoattractants for migrating epithelial cells during organogenesis and wound healing. We present evidence that Rhomboid 3/EGF signalling, which originates from the midline of the Drosophilaventral nerve cord, repels tracheal ganglionic branches and prevents them from crossing it. rho3 acts independently from the main midline repellent Slit, and originates from a different sub-population of midline cells: the VUM neurons. Expression of dominant-negative Egfr or Ras induces midline crosses,whereas activation of the Egfr or Ras in the leading cell of the ganglionic branch can induce premature turns away from the midline. This suggests that the level of Egfr intracellular signalling, rather than the asymmetric activation of the receptor on the cell surface, is an important determinant in ganglionic branch repulsion. We propose that Egfr activation provides a necessary switch for the interpretation of a yet unknown repellent function of the midline.
- Stockholm University Sweden
- Södertörn University Sweden
- Karolinska Institute Sweden
- Umeå University Sweden
Central Nervous System, Epidermal Growth Factor, Serine Endopeptidases, Membrane Proteins, Nerve Tissue Proteins, ErbB Receptors, Proto-Oncogene Proteins c-raf, Repressor Proteins, Trachea, Drosophila melanogaster, Morphogenesis, ras Proteins, Animals, Drosophila Proteins, Eye Proteins, In Situ Hybridization, Body Patterning, Signal Transduction
Central Nervous System, Epidermal Growth Factor, Serine Endopeptidases, Membrane Proteins, Nerve Tissue Proteins, ErbB Receptors, Proto-Oncogene Proteins c-raf, Repressor Proteins, Trachea, Drosophila melanogaster, Morphogenesis, ras Proteins, Animals, Drosophila Proteins, Eye Proteins, In Situ Hybridization, Body Patterning, Signal Transduction
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