Proper nervous system function depends on precise contacts between nerve cells and their targets. The objective of this study is to learn how the development of specific synaptic connections is regulated. We propose cellular, molecular and genetic analyses of the interactions between particular motoneurons and muscle cells in an embryonic vertebrate, the zebrafish. By studying and perturbing the early development of these cells, we will learn how targets function in specifying the formation of synaptic connections. We propose three specific aims: a) We will identify the particular subset of muscle cells with which the motoneurons first interact and characterize their early development, using a variety of molecular markers. From this we will learn how they differentiate and when they express particular genes that may be important for their developmental functions. b) We will ablate and transplant these cells early in development to see if they function in the patterning of body muscle segments. c) We will characterize and study genes expressed by these muscle cells during early development to learn how they may function in the specification of neuromuscular synapses. Although much work has been done to describe how synapses form, very little is known about what regulates the formation of specific synaptic connections; that is, how does a neuron know which cells it should and should not innervate? In humans, neurons sometimes make mistakes. For example, there are a number of congenital defects (such as infantile Muscular Dystrophies) that are due to incorrect connections between nerve cells and their targets. By learning how these connections normally develop we will gain insights into what goes awry to cause developmental abnormalities.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS021132-08
Application #
3401956
Study Section
Neurology B Subcommittee 2 (NEUB)
Project Start
1984-07-01
Project End
1994-03-31
Budget Start
1992-04-01
Budget End
1993-03-31
Support Year
8
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of Oregon
Department
Type
Schools of Arts and Sciences
DUNS #
948117312
City
Eugene
State
OR
Country
United States
Zip Code
97403
Fashena, D; Westerfield, M (1999) Secondary motoneuron axons localize DM-GRASP on their fasciculated segments. J Comp Neurol 406:415-24
Sepich, D S; Wegner, J; O'Shea, S et al. (1998) An altered intron inhibits synthesis of the acetylcholine receptor alpha-subunit in the paralyzed zebrafish mutant nic1. Genetics 148:361-72
Du, S J; Devoto, S H; Westerfield, M et al. (1997) Positive and negative regulation of muscle cell identity by members of the hedgehog and TGF-beta gene families. J Cell Biol 139:145-56
Melancon, E; Liu, D W; Westerfield, M et al. (1997) Pathfinding by identified zebrafish motoneurons in the absence of muscle pioneers. J Neurosci 17:7796-804
Devoto, S H; Melancon, E; Eisen, J S et al. (1996) Identification of separate slow and fast muscle precursor cells in vivo, prior to somite formation. Development 122:3371-80
Reinhard, E; Nedivi, E; Wegner, J et al. (1994) Neural selective activation and temporal regulation of a mammalian GAP-43 promoter in zebrafish. Development 120:1767-75
Sepich, D S; Ho, R K; Westerfield, M (1994) Autonomous expression of the nic1 acetylcholine receptor mutation in zebrafish muscle cells. Dev Biol 161:84-90
Halpern, M E; Ho, R K; Walker, C et al. (1993) Induction of muscle pioneers and floor plate is distinguished by the zebrafish no tail mutation. Cell 75:99-111
Ekker, M; Wegner, J; Akimenko, M A et al. (1992) Coordinate embryonic expression of three zebrafish engrailed genes. Development 116:1001-10
Liu, D W; Westerfield, M (1992) Clustering of muscle acetylcholine receptors requires motoneurons in live embryos, but not in cell culture. J Neurosci 12:1859-66

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