Duplicate zebrafish runx2 orthologues are expressed in developing skeletal elements
- Flores, M.V., Tsang, V.W., Hu, W., Kalev-Zylinska, M., Postlethwait, J., Crosier, P., Crosier, K., and Fisher, S.
- Gene expression patterns : GEP 4(5): 573-581 (Journal)
- Registered Authors
- Crosier, Kathy, Crosier, Phil, Fisher, Shannon, Flores, Maria, Hu, Wenjue, Postlethwait, John H.
- Zebrafish, Runx2, Skeleton, Cartilage, Bone, Chondrocyte, Osteoblast
- MeSH Terms
- Amino Acid Sequence
- Base Sequence
- Bone and Bones/embryology
- Bone and Bones/metabolism*
- Cluster Analysis
- Core Binding Factor Alpha 1 Subunit
- Gene Expression Regulation, Developmental*
- In Situ Hybridization
- Molecular Sequence Data
- Neoplasm Proteins/metabolism*
- Polymorphism, Single-Stranded Conformational
- Radiation Hybrid Mapping
- Reverse Transcriptase Polymerase Chain Reaction
- Sequence Alignment
- Sequence Analysis, DNA
- Sequence Homology
- Transcription Factors/metabolism*
- 15261836 Full text @ Gene Expr. Patterns
Flores, M.V., Tsang, V.W., Hu, W., Kalev-Zylinska, M., Postlethwait, J., Crosier, P., Crosier, K., and Fisher, S. (2004) Duplicate zebrafish runx2 orthologues are expressed in developing skeletal elements. Gene expression patterns : GEP. 4(5):573-581.
The differentiation of cells in the vertebrate skeleton is controlled by a precise genetic program. One crucial regulatory gene in the pathway encodes the transcription factor Runx2, which in mouse is required for differentiation of all osteoblasts and the proper development of a subset of hypertrophic chondrocytes. To explore the differentiation of skeletogenic cells in the model organism zebrafish (Danio rerio), we have identified two orthologues of the mammalian gene, runx2a and runx2b. Both genes share sequence homology and gene structure with the mammalian genes, and map to regions of the zebrafish genome displaying conserved synteny with the region where the human gene is localized. While both genes are expressed in developing skeletal elements, they show evidence of partial divergence in expression pattern, possibly explaining why both orthologues have been retained through teleost evolution.
Genes / Markers
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Engineered Foreign Genes