giant fibre system
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2006 ◽  
Vol 17 (1) ◽  
pp. 31-41 ◽  
Author(s):  
Marcus J. Allen ◽  
Tanja A. Godenschwege ◽  
Mark A. Tanouye ◽  
Pauline Phelan

Development ◽  
2000 ◽  
Vol 127 (23) ◽  
pp. 5203-5212
Author(s):  
K. Jacobs ◽  
M.G. Todman ◽  
M.J. Allen ◽  
J.A. Davies ◽  
J.P. Bacon

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.


Neuroscience ◽  
1999 ◽  
Vol 88 (1) ◽  
pp. 327-336 ◽  
Author(s):  
R Martin ◽  
R Door ◽  
A Ziegler ◽  
W Warchol ◽  
J Hahn ◽  
...  

1986 ◽  
Vol 125 (1) ◽  
pp. 245-269 ◽  
Author(s):  
W. J. Heitler ◽  
K. Fraser

The anatomy and physiology of the segmental giant (SG) neurone of the fourth abdominal ganglion of the hermit crab is described. The SG has an apparently blindending axon in the first root and a small cell body in the anterior ipsilateral ventral quadrant of the ganglion. There is a large ipsilateral neuropile arborization with prominent dendrites lined up along the course of the ipsilateral giant fibre (GF). The SG receives 1:1 input from the ipsilateral GF via an electrical synapse which is usually rectifying. SG activation produces a large EPSP in all ipsilateral and some contralateral fast flexor excitor (FF) motor neurones. The major input to FFs resulting from GF activation appears to be mediated via the SG. It also produces a small EPSP in ipsilateral and contralateral motor giant neurones. The properties of the hermit crab SG are compared to those of the crayfish SG, and the implications of the SG for the possible evolutionary paths of the giant fibre system are discussed.


1983 ◽  
Vol 12 (6) ◽  
pp. 971-991 ◽  
Author(s):  
N. J. Strausfeld ◽  
U. K. Bassemir

1979 ◽  
Vol 32 (2) ◽  
pp. 319-324 ◽  
Author(s):  
Marina Brunetti ◽  
A. Giuditta ◽  
G. Porcellati

1972 ◽  
Vol 43 (2) ◽  
pp. 573-579 ◽  
Author(s):  
Dieter Froesch ◽  
Rainer Martin

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