PUBLICATION

The smad5 mutation somitabun blocks Bmp2b signaling during early dorsoventral patterning of the zebrafish embryo

Authors
Hild, M., Dick, A., Rauch, G.J., Meier, A., Bouwmeester, T., Haffter, P., and Hammerschmidt, M.
ID
ZDB-PUB-990507-8
Date
1999
Source
Development (Cambridge, England)   126(10): 2149-2159 (Journal)
Registered Authors
Dick, Alexander, Haffter, Pascal, Hammerschmidt, Matthias, Hild, Marc, Rauch, Gerd-Jörg
Keywords
smad5; Bmp2/4 signaling; doresoventral patterning; zebrafish
MeSH Terms
  • Base Sequence
  • Phenotype
  • Bone Morphogenetic Protein 4
  • Bone Morphogenetic Proteins/genetics
  • Bone Morphogenetic Proteins/metabolism*
  • Bone Morphogenetic Proteins/pharmacology
  • DNA, Complementary
  • DNA-Binding Proteins/genetics
  • DNA-Binding Proteins/metabolism*
  • Signal Transduction*
  • Body Patterning
  • Zebrafish Proteins
  • Zebrafish
  • Trans-Activators/genetics
  • Trans-Activators/metabolism*
  • Amino Acid Sequence
  • Molecular Sequence Data
  • Smad5 Protein
  • Bone Morphogenetic Protein 2
  • Humans
  • Transforming Growth Factor beta*
  • Genetic Linkage
  • Smad Proteins
  • Animals
  • Phosphoproteins/genetics
  • Phosphoproteins/metabolism*
(all 26)
PubMed
10207140 Full text @ Development
Abstract
Signaling by members of the TGFbeta superfamily is thought to be transduced by Smad proteins. Here, we describe a zebrafish mutant in smad5, designated somitabun (sbn). The dominant maternal and zygotic effect of the sbntc24 mutation is caused by a change in a single amino acid in the L3 loop of Smad5 protein which transforms Smad5 into an antimorphic version, inhibiting wild-type Smad5 and related Smad proteins. sbn mutant embryos are strongly dorsalized, similarly to mutants in Bmp2b, its putative upstream signal. Double mutant analyses and RNA injection experiments show that sbn and bmp2b interact and that sbn acts downstream of Bmp2b signaling to mediate Bmp2b autoregulation during early dorsoventral (D-V) pattern formation. Comparison of early marker gene expression patterns, chimera analyses and rescue experiments involving temporally controlled misexpression of bmp or smad in mutant embryos reveal three phases of D-V patterning: an early sbn- and bmp2b-independent phase when a coarse initial D-V pattern is set up, an intermediate sbn- and bmp2b-dependent phase during which the putative morphogenetic Bmp2/4 gradient is established, and a later sbn-independent phase during gastrulation when the Bmp2/4 gradient is interpreted and cell fates are specified.
Genes / Markers
Figures
Figure Gallery (5 images)
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
dtc24
    Point Mutation
    ta72a
      Point Mutation
      1 - 2 of 2
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      Human Disease / Model
      No data available
      Sequence Targeting Reagents
      No data available
      Fish
      Antibodies
      No data available
      Orthology
      Gene Orthology
      smad5
      1 - 1 of 1
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      Engineered Foreign Genes
      No data available
      Mapping
      No data available