PUBLICATION

A vertebrate-specific and essential role for osterix in osteogenesis revealed by gene knockout in the teleost medaka

Authors
Yu, T., Graf, M., Renn, J., Schartl, M., Larionova, D., Huysseune, A., Witten, P.E., Winkler, C.
ID
ZDB-PUB-170928-21
Date
2017
Source
Development (Cambridge, England)   144: 265-271 (Journal)
Registered Authors
Graf, Martin, Huysseune, Ann, Renn, Joerg, Schartl, Manfred, Winkler, Christoph, Witten, P. Eckhard
Keywords
Bone modelling, Medaka, Osteoblasts, Osteogenesis, Skeleton
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Calcification, Physiologic/genetics
  • Gene Expression Regulation, Developmental
  • Gene Knockout Techniques
  • Notochord/embryology
  • Oryzias/embryology*
  • Oryzias/genetics*
  • Osteogenesis/genetics*
  • Phylogeny
  • Species Specificity
  • Transcription Factors/genetics
  • Transcription Factors/physiology*
  • Vertebrates/embryology
  • Vertebrates/genetics
  • Zebrafish Proteins/physiology
PubMed
27993982 Full text @ Development
Abstract
osterix (osx; sp7) encodes a zinc-finger transcription factor that controls osteoblast differentiation in mammals. Although identified in all vertebrate lineages, its role in non-mammalian bone formation remains elusive. Here, we show that an osx mutation in medaka results in severe bone defects and larval lethality. Pre-osteoblasts fail to differentiate leading to severe intramembranous and perichondral ossification defects. The notochord sheath mineralizes normally, supporting the idea of an osteoblast-independent mechanism for teleost vertebral centra formation. This study establishes a key role for Osx for bone formation in a non-mammalian species, and reveals conserved and non-conserved features in vertebrate bone formation.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping