PUBLICATION

Equivalent genetic roles for bmp7/snailhouse and bmp2b/swirl in dorsoventral pattern formation

Authors
Schmid, B., Fürthauer, M., Connors, S.A., Trout, J., Thisse, B., Thisse, C., and Mullins, M.C.
ID
ZDB-PUB-000309-43
Date
2000
Source
Development (Cambridge, England)   127(5): 957-967 (Journal)
Registered Authors
Connors, Stephanie A., Fürthauer, Maximilian, Mullins, Mary C., Schmid, Bettina, Thisse, Bernard, Thisse, Christine, Trout, Jamie
Keywords
dorsoventral; pattern formation; Bmp7; Bmp2b; TGFß; zebrafish
MeSH Terms
  • Body Patterning/genetics*
  • Bone Morphogenetic Protein 2
  • Bone Morphogenetic Protein 7
  • Cloning, Molecular
  • Zebrafish/embryology*
  • Zebrafish/genetics
  • Phenotype
  • Mutation
  • Amino Acid Sequence
  • Gene Deletion
  • Animals
  • Chromosome Mapping
  • Molecular Sequence Data
  • Zebrafish Proteins*
  • Embryo, Nonmammalian/physiology*
  • Transforming Growth Factor beta*
  • Mutagenesis
  • Sequence Homology, Amino Acid
  • Bone Morphogenetic Proteins/chemistry
  • Bone Morphogenetic Proteins/genetics
  • Bone Morphogenetic Proteins/physiology*
  • Recombinant Proteins/chemistry
  • Transcription, Genetic
  • Sequence Alignment
(all 24)
PubMed
10662635 Full text @ Development
Abstract
A bone morphogenetic protein (BMP) signaling pathway acts in the establishment of the dorsoventral axis of the vertebrate embryo. Here we demonstrate the genetic requirement for two different Bmp ligand subclass genes for dorsoventral pattern formation of the zebrafish embryo. From the relative efficiencies observed in Bmp ligand rescue experiments, conserved chromosomal synteny, and isolation of the zebrafish bmp7 gene, we determined that the strongly dorsalized snailhouse mutant phenotype is caused by a mutation in the bmp7 gene. We show that the original snailhouse allele is a hypomorphic mutation and we identify a snailhouse/bmp7 null mutant. We demonstrate that the snailhouse/bmp7 null mutant phenotype is identical to the presumptive null mutant phenotype of the strongest dorsalized zebrafish mutant swirl/bmp2b, revealing equivalent genetic roles for these two Bmp ligands. Double mutant snailhouse/bmp7; swirl/bmp2b embryos do not exhibit additional or stronger dorsalized phenotypes, indicating that these Bmp ligands do not function redundantly in early embryonic development. Furthermore, overexpression experiments reveal that Bmp2b and Bmp7 synergize in the ventralization of wild-type embryos through a cell-autonomous mechanism, suggesting that Bmp2b/Bmp7 heterodimers may act in vivo to specify ventral cell fates in the zebrafish embryo.
Genes / Markers
Figures
Figure Gallery (7 images)
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
dtc24
    Point Mutation
    p11
      Deficiency
      p15
        Deficiency
        sb1aub
          Point Mutation
          ta72a
            Point Mutation
            tc300a
              Point Mutation
              ty68a
                Point Mutation
                1 - 7 of 7
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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
                No data available
                Mapping
                No data available