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ZFIN ID: ZDB-PUB-040726-7
An Integrin-Dependent Role of Pouch Endoderm in Hyoid Cartilage Development
Crump, J.G., Swartz, M.E., and Kimmel, C.B.
Date: 2004
Source: PLoS Biology 2(9): E244 (Journal)
Registered Authors: Crump, Gage DeKoeyer, Kimmel, Charles B., Swartz, Mary
Keywords: Cartilage, Endoderm, Embryos, Zebrafish, Neural crest, Cartilage development, Apoptosis, Phenotypes
MeSH Terms:
  • Animals
  • Body Patterning
  • Cartilage/embryology
  • Cartilage/metabolism
  • Cartilage/pathology
  • Cell Lineage
  • Electroporation
  • Endoderm/metabolism*
  • Evolution, Molecular
  • Gene Expression Regulation, Developmental*
  • Green Fluorescent Proteins/metabolism
  • Hyoid Bone/embryology
  • Hyoid Bone/growth & development*
  • Integrin alpha5/genetics*
  • Integrins/metabolism*
  • Microscopy, Confocal
  • Models, Biological
  • Molecular Sequence Data
  • Mutation*
  • Neural Crest/metabolism
  • Neurons/metabolism
  • Phenotype
  • Time Factors
  • Zebrafish
  • Zebrafish Proteins/chemistry
PubMed: 15269787 Full text @ PLoS Biol.
Pharyngeal endoderm is essential for and can reprogram development of the head skeleton. Here we investigate the roles of specific endodermal structures in regulating craniofacial development. We have isolated an integrinalpha5 mutant in zebrafish that has region-specific losses of facial cartilages derived from hyoid neural crest cells. In addition, the cranial muscles that normally attach to the affected cartilage region and their associated nerve are secondarily reduced in integrinalpha5- animals. Earlier in development, integrinalpha5 mutants also have specific defects in the formation of the first pouch, an outpocketing of the pharyngeal endoderm. By fate mapping, we show that the cartilage regions that are lost in integrinalpha5 mutants develop from neural crest cells directly adjacent to the first pouch in wild-type animals. Furthermore, we demonstrate that Integrinalpha5 functions in the endoderm to control pouch formation and cartilage development. Time-lapse recordings suggest that the first pouch promotes region-specific cartilage development by regulating the local compaction and survival of skeletogenic neural crest cells. Thus, our results reveal a hierarchy of tissue interactions, at the top of which is the first endodermal pouch, which locally coordinates the development of multiple tissues in a specific region of the vertebrate face. Lastly, we discuss the implications of a mosaic assembly of the facial skeleton for the evolution of ray-finned fish.