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Regulation of synaptic connectivity: levels of fasciclin II influence synaptic growth in the Drosophila CNS

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Baines, Richard A., Seugnet, Laurent, Thompson, Annemarie, Salvaterra, Paul M. and Bate, Michael. (2002) Regulation of synaptic connectivity: levels of fasciclin II influence synaptic growth in the Drosophila CNS. Journal of Neuroscience, Vol.22 (No.15). pp. 6587-6595. ISSN 0270-6474

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Official URL: http://www.jneurosci.org/cgi/content/full/22/15/65...

Abstract

Much of our understanding of synaptogenesis comes from studies that deal with the development of the neuromuscular junction (NMJ). Although well studied, it is not clear how far the NMJ represents an adequate model for the formation of synapses within the CNS. Here we investigate the role of Fasciclin II (Fas II) in the development of synapses between identified motor neurons and cholinergic interneurons in the CNS of Drosophila. Fas II is a neural cell adhesion molecule homolog that is involved in both target selection and synaptic plasticity at the NMJ in Drosophila. In this study, we show that levels of Fas II are critical determinants of synapse formation and growth in the CNS. The initial establishment of synaptic contacts between these identified neurons is seemingly independent of Fas II. The subsequent proliferation of these synaptic connections that occurs postembryonically is, in contrast, significantly retarded by the absence of Fas II. Although the initial formation of synaptic connectivity between these neurons is seemingly independent of Fas II, we show that their formation is, nevertheless, significantly affected by manipulations that alter the relative balance of Fas II in the presynaptic and postsynaptic neurons. Increasing expression of Fas II in either the presynaptic or postsynaptic neurons, during embryogenesis, is sufficient to disrupt the normal level of synaptic connectivity that occurs between these neurons. This effect of Fas II is isoform specific and, moreover, phenocopies the disruption to synaptic connectivity observed previously after tetanus toxin light chain-dependent blockade of evoked synaptic vesicle release in these neurons.

Item Type: Journal Article
Subjects: R Medicine > RC Internal medicine > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry
Q Science > QL Zoology
Divisions: Faculty of Science > Life Sciences (2010- ) > Biological Sciences ( -2010)
Library of Congress Subject Headings (LCSH): Drosophila -- Physiology, Synapses -- Research, Tetanus toxin, Neuroplasticity, Motor neurons
Journal or Publication Title: Journal of Neuroscience
Publisher: Society for Neuroscience
ISSN: 0270-6474
Date: 1 August 2002
Volume: Vol.22
Number: No.15
Page Range: pp. 6587-6595
Status: Peer Reviewed
Access rights to Published version: Open Access
Funder: Royal Society (Great Britain), Wellcome Trust (London, England)
References: Bailey CH, Chen M, Keller F, Kandel ER (1992) Serotonin-mediated endocytosis of apCAM: an early step of learning-related synaptic growth in Aplysia. Science 256:645–649. Baines RA, Bate M (1998) Electrophysiological development of central neurons in the Drosophila embryo. J Neurosci 18:4673–4683. Baines RA, Robinson SG, Fujioka M, Jaynes JB, Bate M (1999) Postsynaptic vesicle release is essential for synaptogenesis in Drosophila. Curr Biol 9:1267–1270. Baines RA, Uhler JP, Thompson A, Sweeney ST, Bate M (2001) Altered electrical properties in Drosophila neurons developing without synaptic transmission. J Neurosci 21:1523–1531. Cheng Y, Endo K, Wu K, Rodan AR, Heberlein U, Davis RL (2001) Drosophila fasciclinII is required for the formation of odor memories and for normal sensitivity to alcohol. Cell 105:757–768. Chiba A (1999) Early development of the Drosophila neuromuscular junction: a model for studying neuronal networks in development. Int Rev Neurobiol 43:1–24. Davis GW, Goodman CS (1998) Synapse-specific control of synaptic efficacy at the terminals of a single neuron. Nature 392:82–86. Davis GW, Schuster CM, Goodman CS (1997) Genetic analysis of the mechanisms controlling target selection: target-derived Fasciclin II regulates the pattern of synapse formation. Neuron 19:561–573. Dityatev A, Dityateva G, Schachner M (2000) Synaptic strength as a function of post- versus presynaptic expression of the neural cell adhesion molecule NCAM. Neuron 26:207–217. Fujioka M, Emi-Sarker Y, Yusibova GL, Goto T, Jaynes JB (1999) Analysis of an even-skipped rescue transgene reveals both composite and discrete neuronal and early blastoderm enhancers, and multi-stripe positioning by gap gene repressor gradients. Development 126:2527–2538. Ghysen A, O’Kane C (1989) Neural enhancer-like elements as specific cell markers in Drosophila. Development 105:35–52. Goodman CS, Shatz CJ (1993) Developmental mechanisms that generate precise patterns of neuronal connectivity. Cell 72:77–98. Goodman CS, Davis GW, Zito K (1997) The many faces of Fasciclin II: genetic analysis reveals multiple roles for a cell adhesion molecule during the generation of neuronal specificity. Cold Spring Harb Symp Quant Biol 62:479–491. Grenningloh G, Bieber A, Rehm J, Snow PM, Traquina Z, Hortsch M, Patel NH, Goodman CS (1990) Molecular genetics of neuronal recognition in Drosophila: evolution and function of immunoglobulin superfamily cell adhesion molecules. Cold Spring Harbor Symp Quant Biol 55:327–340. Grenningloh G, Rehm EJ, Goodman CS (1991) Genetic analysis of growth cone guidance in Drosophila: Fasciclin II functions as a neuronal recognition molecule. Cell 67:45–57. Haverkamp LJ (1986) Anatomical and physiological development of the Xenopus embryonic motor system in the absence of neural activity. J Neurosci 6:1338–1348. Haverkamp LJ, Oppenheim RW (1986) Behavioral development in the absence of neural activity: effects of chronic immobilization on amphibian embryos. J Neurosci 6:1332–1337. Hiesinger PR, Reiter C, Schau H, Fischbach K-F (1999) Neuropil pattern formation and regulation of cell adhesion molecules in Drosophila optic lobe development depend on synaptobrevin. J Neurosci 19:7548–7556. Katz LC, Shatz CJ (1996) Synaptic activity and the construction of cortical circuits. Science 274:1133–1138. Lin DM, Fetter RD, Kopczynski C, Grenningloh G, Goodman CS (1994) Genetic analysis of Fasciclin II in Drosophila: defasciculation, refasciculation, and altered fasciculation. Neuron 13:1055–1069. Mayford M, Barzilai A, Keller F, Schacher S, Kandel ER (1992) Modulation of an NCAM-related adhesion molecule with long-term synaptic plasticity in Aplysia. Science 256:638–643. Rechsteiner M (1988) Regulation of enzyme levels by proteolysis: the role of PEST regions. Adv Enzyme Regul 27:135–151. Salvaterra PM, Kitamoto T (2001) Drosophila cholinergic neurons and processes visualized with Gal4/UAS-GFP. Gene Expr Patterns 1:73–82. Schuster CM, Davis GW, Fetter RD, Goodman CS (1996a) Genetic dissection and functional components of synaptic plasticity. I. Fasciclin II controls synaptic stabilisation and growth. Neuron 17:641–654. Schuster CM, Davis GW, Fetter RD, Goodman CS (1996b) Genetic dissection and functional components of synaptic plasticity. II. Fasciclin II controls presynaptic structural plasticity. Neuron 17:655–667. Sweeney ST, Broadie K, Keane J, Niemann H, O’Kane J (1995) Targeted expression of tetanus toxin light chain in Drosophila specifically eliminates synaptic transmission and causes behavioral defects. Neuron 14:341–351. Turrigiano GG (2000) AMPA receptors unbound: membrane cycling and synaptic plasticity. Neuron 26:5–8. Uhler JP (2001) The development of dendritic arbors in Drosophila motoneurons, PhD thesis. University of Cambridge. Van Vactor D, Sink H, Famborough D, Tsoo R, Goodman CS (1993) Genes that control neuromuscular specificity in Drosophila. Cell 73:1137–1153. Zhu H,Wu F, Schacher S (1995) Changes in expression and distribution of Aplysia cell adhesion molecules can influence synapse formation and elimination in vitro. J Neurosci 15:4173–4183.
URI: http://wrap.warwick.ac.uk/id/eprint/2557

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