Roles for GFRα1 receptors in zebrafish enteric nervous system development
Author:
Shepherd Iain T.12, Pietsch Jacy2, Elworthy Stone3, Kelsh Robert N.3, Raible David W.1
Affiliation:
1. Department of Biological Structure, University of Washington, Box 357420,Seattle, WA 98195, USA 2. Department of Biology, Emory University, Rollins Research Center, 1510 Clifton Road, Atlanta GA 30322, USA 3. Centre for Regenerative Medicine and Developmental Biology Program, Department of Biology and Biochemistry, University of Bath, Bath BA2 7AY, UK
Abstract
Components of the zebrafish GDNF receptor complex are expressed very early in the development of enteric nervous system precursors, and are already present as these cells begin to enter the gut and migrate caudally along its length. Both gfra1a and gfra1b as well as ret are expressed at this time, while gfra2 expression, the receptor component that binds the GDNF-related ligand neurturin, is not detected until the precursors have migrated along the gut. Gfra genes are also expressed in regions of the zebrafish brain and peripheral ganglia, expression domains conserved with other species. Enteric neurons are eliminated after injection with antisense morpholino oligonucleotides against ret or against both Gfra1 orthologs, but are not affected by antisense oligonucleotides against gfra2. Blocking GDNF signaling prevents migration of enteric neuron precursors, which remain positioned at the anterior end of the gut. Phenotypes induced by injection of antisense morpholinos against both Gfra orthologs can be rescued by introduction of mRNA for gfra1a or for gfra2, suggesting that GFRα1 and GFRα2 are functionally equivalent.
Publisher
The Company of Biologists
Subject
Developmental Biology,Molecular Biology
Reference73 articles.
1. Airaksinen, M. S., Titievsky, A. and Saarma, M.(1999). GDNF family neurotrophic factor signaling: four masters,one servant? Mol. Cell. Neurosci.13,313-325. 2. Arenas, E., Trupp, M., Akerud, P. and Ibanez, C. F.(1995). GDNF prevents degeneration and promotes the phenotype of brain noradrenergic neurons in vivo. Neuron15,1465-1473. 3. Baloh, R. H., Tansey, M. G., Golden, J. P., Creedon, D. J.,Heuckeroth, R. O., Keck, C. L., Zimonjic, D. B., Popescu, N. C., Johnson, E. M., Jr and Milbrandt, J. (1997). TrnR2, a novel receptor that mediates neurturin and GDNF signaling through Ret. Neuron18,793-802. 4. Baloh, R. H., Gorodinsky, A., Golden, J. P., Tansey, M. G.,Keck, C. L., Popescu, N. C., Johnson, E. M., Jr and Milbrandt, J.(1998a). GFRalpha3 is an orphan member of the GDNF/neurturin/persephin receptor family. Proc. Natl. Acad. Sci. USA95,5801-5806. 5. Baloh, R. H., Tansey, M. G., Lampe, P. A., Fahrner, T. J.,Enomoto, H., Simburger, K. S., Leitner, M. L., Araki, T., Johnson, E. M., Jr and Milbrandt, J. (1998b). Artemin, a novel member of the GDNF ligand family, supports peripheral and central neurons and signals through the GFRalpha3-RET receptor complex. Neuron21,1291-1302.
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