Multiple regulatory elements with spatially and temporally distinct activities control neurogenin1 expression in primary neurons of the zebrafish embryo
- Blader, P., Plessy, C., and Strähle, U.
- Mechanisms of Development 120(2): 211-218 (Journal)
- Registered Authors
- Blader, Patrick, Plessy, Charles, Strähle, Uwe
- Neurogenin1; Primary neurons; Zebrafish; Neurogenesis; Transgenesis; Enhancer
- MeSH Terms
- Amino Acid Sequence
- Basic Helix-Loop-Helix Transcription Factors
- Bone Morphogenetic Protein 2
- Bone Morphogenetic Proteins/genetics
- Bone Morphogenetic Proteins/metabolism
- Conserved Sequence
- Embryo, Nonmammalian
- Gene Expression Regulation, Developmental
- Molecular Sequence Data
- Nerve Tissue Proteins/genetics*
- Nerve Tissue Proteins/metabolism
- Nervous System/embryology
- Regulatory Sequences, Nucleic Acid*
- Signal Transduction
- Transcription Factors/genetics*
- Transcription Factors/metabolism
- Zebrafish Proteins/genetics*
- Zebrafish Proteins/metabolism
- 12559493 Full text @ Mech. Dev.
Blader, P., Plessy, C., and Strähle, U. (2003) Multiple regulatory elements with spatially and temporally distinct activities control neurogenin1 expression in primary neurons of the zebrafish embryo. Mechanisms of Development. 120(2):211-218.
The basic Helix-Loop-Helix gene neurogenin1 (ngn1) is expressed in a complex pattern in the neural plate of zebrafish embryos, demarcating the sites of primary neurogenesis. We have dissected the ngn1 locus to identify cis-regulatory regions that control this expression. We have isolated two upstream elements that drive expression in precursors of Rohon-Beard sensory neurons and hindbrain interneurons and in clusters of neuronal precursors in the anterior neural plate, respectively. A third regulatory region mediates later expression. Thus, regulatory sequences with temporally and spatially distinct activities control ngn1 expression in primary neurons of the zebrafish embryo. These regions are highly similar to 5' sequences in the mouse and human ngn1 gene, suggesting that amniote embryos, despite lacking primary neurons, utilize related mechanism to control ngn1 expression.
Genes / Markers
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Engineered Foreign Genes