PUBLICATION

Role of mef2ca in developmental buffering of the zebrafish larval hyoid dermal skeleton

Authors
Delaurier, A., Huycke, T.R., Nichols, J.T., Swartz, M.E., Larsen, A., Walker, C., Dowd, J., Pan, L., Moens, C.B., and Kimmel, C.B.
ID
ZDB-PUB-140108-17
Date
2014
Source
Developmental Biology   385(2): 189-99 (Journal)
Registered Authors
DeLaurier, April, Dowd, John, Huycke, Tyler, Kimmel, Charles B., Moens, Cecilia, Nichols, James Tucker, Pan, Luyuan, Swartz, Mary, Walker, Charline
Keywords
Canalization, Developmental instability, Osteoblast, Pharyngeal arch, Skeleton, mef2c
MeSH Terms
  • Zebrafish Proteins/genetics*
  • Genes, Homeobox
  • Bone Development/genetics*
  • Zebrafish/embryology*
  • Zebrafish/genetics
  • Zebrafish/growth & development
  • Animals
  • Larva/growth & development*
(all 8)
PubMed
24269905 Full text @ Dev. Biol.
Abstract

Phenotypic robustness requires a process of developmental buffering that is largely not understood, but which can be disrupted by mutations. Here we show that in mef2cab1086 loss of function mutant embryos and early larvae, development of craniofacial hyoid bones, the opercle (Op) and branchiostegal ray (BR), becomes remarkably unstable; the large magnitude of the instability serves as a positive attribute to learn about features of this developmental buffering. The OpBR mutant phenotype variably includes bone expansion and fusion, Op duplication, and BR homeosis. Formation of a novel bone strut, or a bone bridge connecting the Op and BR together occurs frequently. We find no evidence that the phenotypic stability in the wild type is provided by redundancy between mef2ca and its co-ortholog mef2cb, or that it is related to the selector (homeotic) gene function of mef2ca. Changes in dorsal–ventral patterning of the hyoid arch also might not contribute to phenotypic instability in mutants. However, subsequent development of the bone lineage itself, including osteoblast differentiation and morphogenetic outgrowth, shows marked variation. Hence, steps along the developmental trajectory appear differentially sensitive to the loss of buffering, providing focus for the future study.

Genes / Markers
Figures
Figure Gallery (6 images)
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
b1086
    Point Mutation
    b1212TgTransgenic Insertion
      fh288
        Point Mutation
        j1073aGtTransgenic Insertion
        j1271aGtTransgenic Insertion
        tg419
          Point Mutation
          1 - 6 of 6
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          Human Disease / Model
          No data available
          Sequence Targeting Reagents
          No data available
          Fish
          Antibodies
          No data available
          Orthology
          No data available
          Engineered Foreign Genes
          Marker Marker Type Name
          EGFPEFGEGFP
          1 - 1 of 1
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          Mapping
          No data available