Zebrafish narrowminded disrupts the transcription factor prdm1 and is required for neural crest and sensory neuron specification
Specification of both neural crest cells and Rohon–Beard (RB) sensory neurons involves a complex series of interactions between the neural and non-neural ectoderm. The molecular mechanisms directing this process are not well understood. The zebrafish narrowminded ( nrd) mutation is unique, since it...
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Published in | Developmental biology Vol. 278; no. 2; pp. 347 - 357 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
15.02.2005
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Subjects | |
Online Access | Get full text |
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Summary: | Specification of both neural crest cells and Rohon–Beard (RB) sensory neurons involves a complex series of interactions between the neural and non-neural ectoderm. The molecular mechanisms directing this process are not well understood. The zebrafish
narrowminded (
nrd) mutation is unique, since it is one of two mutations in which defects are observed in both cell populations: it leads to a complete absence of RB neurons and a reduction in neural crest cells and their derivatives. Here, we show that
nrd is a mutation in
prdm1, a SET/zinc-finger domain transcription factor. A Morpholino-mediated depletion of
prdm1 phenocopies the
nrd mutation, and conversely overexpression of
prdm1 mRNA rescues the
nrd RB sensory neuron and neural crest phenotype.
prdm1 is expressed at the border of the neural plate within the domain where neural crest cells and RB sensory neurons form. Analysis of
prdm1 function by overexpression indicates that
prdm1 functions to promote the cell fate specification of both neural crest cells and RB sensory neurons, most likely as a downstream effector of the BMP signaling pathway. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0012-1606 1095-564X |
DOI: | 10.1016/j.ydbio.2004.11.014 |