K Venkatesh1, G Hasan. 1. National Centre for Biological Sciences, TIFR Centre, IISc Campus, P.O. 1234, Bangalore 560012, India.
Abstract
BACKGROUND: The inositol 1,4,5-trisphosphate (IP3) receptor is an intracellular calcium channel that couples cell membrane receptors, via the second messenger IP3, to calcium signal transduction pathways within many types of cells. IP3 receptor function has been implicated in development, but the physiological processes affected by its function have yet to be elucidated. In order to identify these processes, we generated mutants in the IP3 receptor gene (itpr) of Drosophila and studied their phenotype during development. RESULTS: All itpr mutant alleles were lethal. Lethality occurred primarily during the larval stages and was preceded by delayed moulting. Insect moulting occurs in response to the periodic release of the steroid hormone ecdysone which, in Drosophila, is synthesized and secreted by the ring gland. The observation of delayed moulting in the mutants, coupled with the expression of the IP3 receptor in the larval ring gland led us to examine the effect of the itpr alleles on ecdysone levels. On feeding ecdysone to mutant larvae, a partial rescue of the itpr phenotype was observed. In order to assess ecdysone levels at all larval stages, we examined transcripts of an ecdysone-inducible gene, E74; these transcripts were downregulated in larvae expressing each of the itpr alleles. CONCLUSIONS: Our data show that disruption of the Drosophila IP3 receptor gene leads to lowered levels of ecdysone. Synthesis and release of ecdysone from the ring gland is thought to occur in response to a neurosecretory peptide hormone secreted by the brain. We propose that this peptide hormone requires an IP3 signalling pathway for ecdysone synthesis and release in Drosophila and other insects. This signal transduction mechanism which links neuropeptide hormones to steroid hormone secretion might be evolutionarily conserved.
BACKGROUND: The inositol 1,4,5-trisphosphate (IP3) receptor is an intracellular calcium channel that couples cell membrane receptors, via the second messenger IP3, to calcium signal transduction pathways within many types of cells. IP3 receptor function has been implicated in development, but the physiological processes affected by its function have yet to be elucidated. In order to identify these processes, we generated mutants in the IP3 receptor gene (itpr) of Drosophila and studied their phenotype during development. RESULTS: All itpr mutant alleles were lethal. Lethality occurred primarily during the larval stages and was preceded by delayed moulting. Insect moulting occurs in response to the periodic release of the steroid hormoneecdysone which, in Drosophila, is synthesized and secreted by the ring gland. The observation of delayed moulting in the mutants, coupled with the expression of the IP3 receptor in the larval ring gland led us to examine the effect of the itpr alleles on ecdysone levels. On feeding ecdysone to mutant larvae, a partial rescue of the itpr phenotype was observed. In order to assess ecdysone levels at all larval stages, we examined transcripts of an ecdysone-inducible gene, E74; these transcripts were downregulated in larvae expressing each of the itpr alleles. CONCLUSIONS: Our data show that disruption of the DrosophilaIP3 receptor gene leads to lowered levels of ecdysone. Synthesis and release of ecdysone from the ring gland is thought to occur in response to a neurosecretory peptide hormone secreted by the brain. We propose that this peptide hormone requires an IP3 signalling pathway for ecdysone synthesis and release in Drosophila and other insects. This signal transduction mechanism which links neuropeptide hormones to steroid hormone secretion might be evolutionarily conserved.
Authors: I Chorna-Ornan; T Joel-Almagor; H C Ben-Ami; S Frechter; B Gillo; Z Selinger; D L Gill; B Minke Journal: J Neurosci Date: 2001-04-15 Impact factor: 6.167