Novel level of signalling control in the JAK/STAT pathway revealed by in situ visualisation of protein-protein interaction duringDrosophiladevelopment
Open Access
- 15 July 2003
- journal article
- Published by The Company of Biologists in Development
- Vol. 130 (14) , 3077-3084
- https://doi.org/10.1242/dev.00535
Abstract
It is commonly accepted that activation of most signalling pathways is induced by ligand receptor dimerisation. This belief has been challenged for some vertebrate cytokine receptors of the JAK/STAT pathway. Here we study whether DOME, the Drosophila receptor of the JAK/STAT pathway, can dimerise and if the dimerisation is ligand-dependent. To analyse DOME homo-dimerisation, we have applied a β-gal complementation technique that allows the detection of protein interactions in situ. This technique has been used previously in cell culture but this is the first time that it has been applied to whole embryos. We show that this technique, which we renameβ lue-βlau technique, can be used to detect DOME homo-dimerisation in Drosophila developing embryos. Despite DOME being ubiquitously expressed, dimerisation is developmentally regulated. We investigate the state of DOME dimerisation in the presence or absence of ligand and show that DOME dimerisation is not ligand-induced, indicating that ligand independent cytokine receptor dimerisation is a conserved feature across phyla. We have further analysed the functional significance of ligand-independent receptor dimerisation by comparing the effects of ectopic ligand expression in cells in which the receptor is, or is not, dimerised. We show that ligand expression can only activate STAT downstream targets or affect embryo development in cells in which the receptor is dimerised. These results suggest a model in which ligand-independent dimerisation of the JAK/STAT receptor confers cells with competence to activate the pathway prior to ligand reception. Thus, competence to induce the JAK/STAT signalling pathway in Drosophila can be regulated by controlling receptor dimerisation prior to ligand binding. These results reveal a novel level of JAK/STAT signalling regulation that could also apply to vertebrates.Keywords
This publication has 39 references indexed in Scilit:
- The Fertile Field of Drosophila JAK/STAT SignallingCurrent Biology, 2002
- Ligand-independent Dimer Formation of Epidermal Growth Factor Receptor (EGFR) Is a Step Separable from Ligand-induced EGFR SignalingMolecular Biology of the Cell, 2002
- Monitoring of Ligand-independent Dimerization and Ligand-induced Conformational Changes of Melatonin Receptors in Living Cells by Bioluminescence Resonance Energy TransferJournal of Biological Chemistry, 2002
- Visualization of Interactions among bZIP and Rel Family Proteins in Living Cells Using Bimolecular Fluorescence ComplementationMolecular Cell, 2002
- Paracrine signaling through the JAK/STAT pathway activates invasive behavior of ovarian epithelial cells in Drosophila.Published by Elsevier ,2001
- Identification of the first invertebrate interleukin JAK/STAT receptor, the Drosophila gene domelessCurrent Biology, 2001
- Activation of preformed EGF receptor dimers by ligand-induced rotation of the transmembrane domain11Edited by B. HollandJournal of Molecular Biology, 2001
- Identification of a Stat Gene That Functions in Drosophila DevelopmentCell, 1996
- marelle Acts Downstream of the Drosophila HOP/JAK Kinase and Encodes a Protein Similar to the Mammalian STATsCell, 1996
- Interleukin-6 triggers the association of its receptor with a possible signal transducer, gp130Cell, 1989