Literature DB >> 11060245

Synaptogenesis in the giant-fibre system of Drosophila: interaction of the giant fibre and its major motorneuronal target.

K Jacobs1, M G Todman, M J Allen, J A Davies, J P Bacon.   

Abstract

The tergotrochanteral (jump) motorneuron is a major synaptic target of the Giant Fibre in Drosophila. These two neurons are major components of the fly's Giant-Fibre escape system. Our previous work has described the development of the Giant Fibre in early metamorphosis and the involvement of the shaking-B locus in the formation of its electrical synapses. In the present study, we have investigated the development of the tergotrochanteral motorneuron and its electrical synapses by transforming Drosophila with a Gal4 fusion construct containing sequences largely upstream of, but including, the shaking-B(lethal) promoter. This construct drives reporter gene expression in the tergotrochanteral motorneuron and some other neurons. Expression of green fluorescent protein in the motorneuron allows visualization of its cell body and its subsequent intracellular staining with Lucifer Yellow. These preparations provide high-resolution data on motorneuron morphogenesis during the first half of pupal development. Dye-coupling reveals onset of gap-junction formation between the tergotrochanteral motorneuron and other neurons of the Giant-Fibre System. The medial dendrite of the tergotrochanteral motorneuron becomes dye-coupled to the peripheral synapsing interneurons between 28 and 32 hours after puparium formation. Dye-coupling between tergotrochanteral motorneuron and Giant Fibre is first seen at 42 hours after puparium formation. All dye coupling is abolished in a shaking-B(neural) mutant. To investigate any interactions between the Giant Fibre and the tergotroachanteral motorneuron, we arrested the growth of the motorneuron's medial neurite by targeted expression of a constitutively active form of Dcdc42. This results in the Giant Fibre remaining stranded at the midline, unable to make its characteristic bend. We conclude that Giant Fibre morphogenesis normally relies on fasciculation with its major motorneuronal target.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11060245     DOI: 10.1242/dev.127.23.5203

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  19 in total

1.  Dendritic remodeling and growth of motoneurons during metamorphosis of Drosophila melanogaster.

Authors:  Christos Consoulas; Linda L Restifo; Richard B Levine
Journal:  J Neurosci       Date:  2002-06-15       Impact factor: 6.167

2.  Heteromerization of innexin gap junction proteins regulates epithelial tissue organization in Drosophila.

Authors:  Corinna Lehmann; Hildegard Lechner; Birgit Löer; Martin Knieps; Sonja Herrmann; Michael Famulok; Reinhard Bauer; Michael Hoch
Journal:  Mol Biol Cell       Date:  2006-01-25       Impact factor: 4.138

3.  Identifying and monitoring neurons that undergo metamorphosis-regulated cell death (metamorphoptosis) by a neuron-specific caspase sensor (Casor) in Drosophila melanogaster.

Authors:  Gyunghee Lee; Jaeman Kim; Yujin Kim; Siuk Yoo; Jae H Park
Journal:  Apoptosis       Date:  2018-01       Impact factor: 4.677

4.  Application for the Drosophila ventral nerve cord standard in neuronal circuit reconstruction and in-depth analysis of mutant morphology.

Authors:  Jana Boerner; Tanja Angela Godenschwege
Journal:  J Neurogenet       Date:  2010-09       Impact factor: 1.250

5.  Structure-function analyses of tyrosine phosphatase PTP69D in giant fiber synapse formation of Drosophila.

Authors:  LaTasha H Lee; Tanja A Godenschwege
Journal:  Mol Cell Neurosci       Date:  2014-11-26       Impact factor: 4.314

6.  Axon Termination, Pruning, and Synaptogenesis in the Giant Fiber System of Drosophila melanogaster Is Promoted by Highwire.

Authors:  Melissa Borgen; Kimberly Rowland; Jana Boerner; Brandon Lloyd; Aruna Khan; Rodney Murphey
Journal:  Genetics       Date:  2017-01-18       Impact factor: 4.562

7.  Gap junction proteins expressed during development are required for adult neural function in the Drosophila optic lamina.

Authors:  Kathryn D Curtin; Zhan Zhang; Robert J Wyman
Journal:  J Neurosci       Date:  2002-08-15       Impact factor: 6.167

8.  CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila.

Authors:  Biljana Ermanoska; William W Motley; Ricardo Leitão-Gonçalves; Bob Asselbergh; LaTasha H Lee; Peter De Rijk; Kristel Sleegers; Tinne Ooms; Tanja A Godenschwege; Vincent Timmerman; Kenneth H Fischbeck; Albena Jordanova
Journal:  Neurobiol Dis       Date:  2014-05-05       Impact factor: 5.996

9.  A modifier screen in the Drosophila eye reveals that aPKC interacts with Glued during central synapse formation.

Authors:  Lisha Ma; Louise A Johns; Marcus J Allen
Journal:  BMC Genet       Date:  2009-11-30       Impact factor: 2.797

10.  Loss of flight and associated neuronal rhythmicity in inositol 1,4,5-trisphosphate receptor mutants of Drosophila.

Authors:  Santanu Banerjee; Jisue Lee; K Venkatesh; Chun-Fang Wu; Gaiti Hasan
Journal:  J Neurosci       Date:  2004-09-08       Impact factor: 6.167

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.