PUBLICATION

Structural requirements for PACSIN/Syndapin operation during zebrafish embryonic notochord development

Authors
Edeling, M.A., Sanker, S., Shima, T., Umasankar, P.K., Höning, S., Kim, H.Y., Davidson, L.A., Watkins, S.C., Tsang, M., Owen, D.J., and Traub, L.M.
ID
ZDB-PUB-091215-55
Date
2009
Source
PLoS One   4(12): e8150 (Journal)
Registered Authors
Shima, Takaki, Tsang, Michael
Keywords
Embryos, Notochords, Zebrafish, Liposomes, Drosophila melanogaster, Dimers (Chemical physics), Cell membranes, Endocytosis
MeSH Terms
  • Notochord/abnormalities
  • Notochord/drug effects
  • Notochord/embryology*
  • Notochord/pathology
  • Carrier Proteins/chemistry*
  • Carrier Proteins/metabolism*
  • Liposomes/metabolism
  • Zebrafish/embryology*
  • Amino Acid Sequence
  • Molecular Sequence Data
  • Protein Binding/drug effects
  • Phenotype
  • Animals
  • Embryo, Nonmammalian/abnormalities
  • Embryo, Nonmammalian/pathology
  • Embryo, Nonmammalian/ultrastructure
  • Cell Movement/drug effects
  • Oligonucleotides, Antisense/pharmacology
  • Protein Structure, Tertiary
  • Zebrafish Proteins/chemistry*
  • Zebrafish Proteins/metabolism*
  • Structure-Activity Relationship
  • Humans
  • Embryonic Development*/drug effects
  • HeLa Cells
PubMed
19997509 Full text @ PLoS One
Abstract
PACSIN/Syndapin proteins are membrane-active scaffolds that participate in endocytosis. The structure of the Drosophila Syndapin N-terminal EFC domain reveals a crescent shaped antiparallel dimer with a high affinity for phosphoinositides and a unique membrane-inserting prong upon the concave surface. Combined structural, biochemical and reverse genetic approaches in zebrafish define an important role for Syndapin orthologue, Pacsin3, in the early formation of the notochord during embryonic development. In pacsin3-morphant embryos, midline convergence of notochord precursors is defective as axial mesodermal cells fail to polarize, migrate and differentiate properly. The pacsin3 morphant phenotype of a stunted body axis and contorted trunk is rescued by ectopic expression of Drosophila Syndapin, and depends critically on both the prong that protrudes from the surface of the bowed Syndapin EFC domain and the ability of the antiparallel dimer to bind tightly to phosphoinositides. Our data confirm linkage between directional migration, endocytosis and cell specification during embryonic morphogenesis and highlight a key role for Pacsin3 in this coupling in the notochord.
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Human Disease / Model
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