Targeted expression of tetanus toxin reveals sets of neurons involved in larval locomotion in Drosophila

被引:45
作者
Suster, ML
Martin, JR
Sung, C
Robinow, S
机构
[1] Univ Cambridge, Dept Zool, Cambridge CB2 3EJ, England
[2] Univ Paris 11, CNRS, NAMC, UMR 8620, F-91405 Orsay, France
[3] Univ Hawaii, Dept Zool, Honolulu, HI 96825 USA
来源
JOURNAL OF NEUROBIOLOGY | 2003年 / 55卷 / 02期
关键词
Drosophila; larval locomotion; GAL4/UAS system; TeTxLC expression;
D O I
10.1002/neu.10202
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The Drosophila larva is widely used for studies of neuronal development and function, yet little is known about the neuronal basis of locomotion in this model organism. Drosophila larvae crawl over a plain substrate by performing repetitive waves of forward peristalsis alternated by brief episodes of head swinging and turning. To identify sets of central and peripheral neurons required for the spatial or temporal pattern of larval locomotion, we blocked neurotransmitter release from defined populations of neurons by targeted expression of tetanus toxin light chain (TeTxLC) with the GAL4/UAS system. One hundred fifty GAL4 lines were crossed to a UAS-TeTxLC strain and a motion-analysis system was used to identify larvae with abnormal movement patterns. Five lines were selected that show discrete locomotor defects (i.e., increased turning and pausing) and these defects are correlated with diverse sets of central neurons. One line, 4C-GAL4, caused an unusual circling behavior that is correlated with approximately 200 neurons, including dopaminergic and peptidergic interneurons. Expression of TeTxLC in all dopaminergic and serotonergic but not in peptidergic neurons, caused turning deficits that are similar to those of 4C-GAL4/TeTxLC larvae. The results presented here provide a basis for future genetic studies of motor control in the Drosophila larva. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:233 / 246
页数:14
相关论文
共 56 条
[21]   Single-cell analysis of Drosophila larval neuromuscular synapses [J].
Hoang, B ;
Chiba, A .
DEVELOPMENTAL BIOLOGY, 2001, 229 (01) :55-70
[22]   PHM is required for normal developmental transitions and for biosynthesis of secretory peptides in Drosophila [J].
Jiang, N ;
Kolhekar, AS ;
Jacobs, PS ;
Mains, RE ;
Eipper, BA ;
Taghert, PH .
DEVELOPMENTAL BIOLOGY, 2000, 226 (01) :118-136
[23]   Crawling motor patterns induced by pilocarpine in isolated larval nerve cords of Manduca sexta [J].
Johnston, RM ;
Levine, RB .
JOURNAL OF NEUROPHYSIOLOGY, 1996, 76 (05) :3178-3195
[24]   GENETIC DISSECTION OF MECHANOSENSORY TRANSDUCTION - MECHANORECEPTION-DEFECTIVE MUTATIONS OF DROSOPHILA [J].
KERNAN, M ;
COWAN, D ;
ZUKER, C .
NEURON, 1994, 12 (06) :1195-1206
[25]   Mushroom bodies are not required for courtship behavior by normal and sexually mosaic Drosophila [J].
Kido, A ;
Ito, K .
JOURNAL OF NEUROBIOLOGY, 2002, 52 (04) :302-311
[26]   Muscle founder cells regulate defasciculation and targeting of motor axons in the Drosophila embryo [J].
Landgraf, M ;
Baylies, M ;
Bate, M .
CURRENT BIOLOGY, 1999, 9 (11) :589-592
[27]  
Landgraf M, 1997, J NEUROSCI, V17, P9642
[28]   Mosaic analysis with a repressible cell marker for studies of gene function in neuronal morphogenesis [J].
Lee, T ;
Luo, LQ .
NEURON, 1999, 22 (03) :451-461
[29]   Ectopic G-protein expression in dopamine and serotonin neurons blocks cocaine sensitization in Drosophila melanogaster [J].
Li, H ;
Chaney, S ;
Forte, M ;
Hirsh, J .
CURRENT BIOLOGY, 2000, 10 (04) :211-214
[30]  
Manseau L, 1997, DEV DYNAM, V209, P310, DOI 10.1002/(SICI)1097-0177(199707)209:3<310::AID-AJA6>3.0.CO