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David W Raible

Publications and source records attributed to David W Raible.

20 records · Page 2Linked to original sources

Neurogenin1 defines zebrafish cranial sensory ganglia precursors.

Cells delaminate from epithelial placodes to form sensory ganglia in the vertebrate head. We describe the formation of cranial neurogenic placodes in the zebrafish, Danio rerio, using bHLH transcription factors as molecular markers. A single neurogenin gene, neurogenin1 (ngn1), is required for the development of all zebrafish cranial ganglia, which contrasts with other described vertebrates. Expression of ngn1 delineates zebrafish ganglionic placodes, including trigeminal, lateral line, and epibranchial placodes. In addition, ngn1 is expressed in a subset of cells within the otic vesicle that will delaminate to form the octaval (statoacoustic) ganglion. The trigeminal placode is the first to differentiate, and forms just lateral and adjacent to the neural crest. Expression of ngn1 is transient and prefigures expression of a related bHLH transcription factor, neuroD. Interfering with ngn1 function using a specific antisense morpholino oligonucleotide blocks differentiation of all cranial ganglia but not associated glial cells. Lateral line sensory neuromasts develop independently of ngn1 function, suggesting that two derivatives of lateral line placodes, ganglia and migrating primordia, are under separate genetic control.

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Specification of zebrafish neural crest.

Analysis of neural crest cells in wild-type zebrafish and in isolated mutants has complemented studies in other organisms and has led to a greater understanding of the processes of cell fate and regional specification. Analysis of pigment cell development suggests that neural crest cell fate specification results from a combination of intrinsic cues such as differential expression of transcription factors and external factors such as the Wnts. Whether this model can be generalized to accommodate other neural crest cell fates remains an active area of research. Regional specification of neural crest appears to be coordinated by similar combinations of internal factors such as the hox genes, and extrinsic cues such as retinoic acid and endothelins. There is still a wealth of zebrafish mutations whose molecular bases remain unknown, and it is likely that the revelation of the underlying genes will both broaden and alter our understanding of specification within the neural crest.

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