Abstract
The bHLH transcription factor Neurog1 (Ngn1, Neurod3, neurogenin 1) is involved in neuronal differentiation and cell-type specification in distinct regions of the developing nervous system. Here, transgenic mouse models were developed that use a Bacterial Artificial Chromosome (BAC) containing 208. kb flanking the Neurog1 gene to efficiently drive expression of GFP and Cre in all Neurog1 domains. Two characteristics of Neurog1 gene regulation were uncovered. First, a 4. kb region previously shown to be sufficient for driving expression of a reporter gene to a subset of the Neurog1 pattern in the developing midbrain, hindbrain, and spinal cord is required uniformly for high levels of expression in all Neurog1 domains, even those not originally identified as being regulated by this region. Second, a 0.8. kb enhancer was identified that is sufficient to drive Neurog1-like expression specifically in the ventral neural tube. Furthermore, Neurog1 progenitor cells in the ventral neural tube are largely fated to interneuron lineages rather than to motoneurons. These studies provide new tools for directing tissue specific expression in the developing neural tube, define Neurog1 lineages in the spinal cord, and further define the complex genomic structure required for obtaining the correct levels and spatial restriction of the neuronal differentiation gene Neurog1.
Original language | English (US) |
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Pages (from-to) | 283-292 |
Number of pages | 10 |
Journal | Developmental Biology |
Volume | 340 |
Issue number | 2 |
DOIs | |
State | Published - Apr 2010 |
Keywords
- BAC transgenic mice
- BHLH transcription factor
- Cre recombinase
- Gene regulation
- Neural tube enhancer
- Neurogenesis
- Neurogenin
- Ngn1
- Spinal cord development
- Ventral spinal cord interneurons
ASJC Scopus subject areas
- Molecular Biology
- Developmental Biology
- Cell Biology