PUBLICATION
The zebrafish spiel-ohne-grenzen (spg) gene encodes the POU domain protein Pou2 related to mammalian Oct4 and is essential for formation of the midbrain and hindbrain, and for pre-gastrula morphogenesis
- Authors
- Burgess, S., Reim, G., Chen, W., Hopkins, N., and Brand, M.
- ID
- ZDB-PUB-020306-4
- Date
- 2002
- Source
- Development (Cambridge, England) 129(4): 905-916 (Journal)
- Registered Authors
- Brand, Michael, Burgess, Shawn, Chen, Wenbiao, Hopkins, Nancy, Reim, Gerlinde
- Keywords
- pou2; Oct3/4; pou5f1; isthmus; MHB; organizer; pax2.1; spiel-ohne-grenzen; hindbrain; zebrafish
- MeSH Terms
-
- Alleles
- Animals
- DNA-Binding Proteins/classification
- DNA-Binding Proteins/genetics*
- Early Growth Response Protein 2
- Female
- Gastrula
- Gene Expression
- Male
- Mammals
- Mesencephalon/embryology*
- Morphogenesis
- Mutagenesis
- Octamer Transcription Factor-3
- PAX2 Transcription Factor
- Rhombencephalon/embryology*
- Transcription Factors/classification
- Transcription Factors/genetics*
- Transcription Factors/metabolism*
- Transcription Factors/physiology*
- Zebrafish/classification
- Zebrafish/embryology
- Zebrafish/genetics
- Zebrafish Proteins*
- PubMed
- 11861474 Full text @ Development
Citation
Burgess, S., Reim, G., Chen, W., Hopkins, N., and Brand, M. (2002) The zebrafish spiel-ohne-grenzen (spg) gene encodes the POU domain protein Pou2 related to mammalian Oct4 and is essential for formation of the midbrain and hindbrain, and for pre-gastrula morphogenesis. Development (Cambridge, England). 129(4):905-916.
Abstract
In early embryonic development, the brain is divided into three main regions along the anteroposterior axis: the forebrain, midbrain and hindbrain. Through retroviral insertional mutagenesis and chemical mutagenesis experiments in zebrafish, we have isolated mutations that cause abnormal hindbrain organization and a failure of the midbrain-hindbrain boundary (MHB) to form, a region that acts as an organizer for the adjacent brain regions. The mutations fail to complement the spiel-ohne-grenzen (spg) mutation, which causes a similar phenotype, but for which the affected gene is unknown. We show through genetic mapping, cloning of the proviral insertion site and allele sequencing that spg mutations disrupt pou2, a gene encoding the Pou2 transcription factor. Based on chromosomal synteny, phylogenetic sequence comparison, and expression and functional data, we suggest that pou2 is the zebrafish ortholog of mouse Oct3/Oct4 and human POU5F1. For the mammalian genes, a function in brain development has so far not been described. In the absence of functional pou2, expression of markers for the midbrain, MHB and the hindbrain primordium (pax2.1, wnt1, krox20) are severely reduced, correlating with the neuroectoderm-specific expression phase of pou2. Injection of pou2 mRNA restores these defects in spg mutant embryos, but does not activate these markers ectopically, demonstrating a permissive role for pou2. Injections of pou2-morpholinos phenocopy the spg phenotype at low concentration, further proving that spg encodes pou2. Two observations suggest that pou2 has an additional earlier function: higher pou2-morpholino concentrations specifically cause a pre-gastrula arrest of cell division and morphogenesis, and expression of pou2 mRNA itself is reduced in spg-homozygous embryos at this stage. These experiments suggest two roles for pou2. Initially, Pou2 functions during early proliferation and morphogenesis of the blastomeres, similar to Oct3/4 in mammals during formation of the inner cell mass. During zebrafishbrain formation, Pou2 then functions a second time to activate gene expression in the midbrain and hindbrain primordium, which is reflected at later stages in the specific lack in spg embryos of the MHB and associated defects in the mid- and hindbrain.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping