PUBLICATION

Inca: a novel p21-activated kinase-associated protein required for cranial neural crest development

Authors
Luo, T., Xu, Y., Hoffman, T.L., Zhang, T., Schilling, T., and Sargent, T.D.
ID
ZDB-PUB-070303-29
Date
2007
Source
Development (Cambridge, England)   134(7): 1279-1289 (Journal)
Registered Authors
Luo, Ting, Sargent, Tom, Schilling, Tom
Keywords
Cartilage, PAK, Cortical actin, Cytoskeleton, Wound healing, Craniofacial, Tfap2a, Ectomesenchyme, Neural crest, Xenopus, Zebrafish
MeSH Terms
  • Blotting, Western
  • Molecular Sequence Data
  • Anura/embryology
  • Xenopus/embryology*
  • Xenopus/metabolism
  • Immunoprecipitation
  • In Situ Nick-End Labeling
  • Animals
  • In Situ Hybridization
  • Gene Expression Regulation, Developmental*
  • Mice
  • Skull/embryology*
  • Neural Crest/embryology*
  • Actins/metabolism
  • Cell Adhesion/physiology
  • Yeasts
  • Xenopus Proteins/genetics*
  • Xenopus Proteins/metabolism
  • Zebrafish/embryology
  • Transcription Factor AP-2/metabolism
  • Cell Movement/physiology
  • Microarray Analysis
  • Amino Acid Sequence
  • p21-Activated Kinases/metabolism
  • Nerve Tissue Proteins/genetics*
  • Nerve Tissue Proteins/metabolism
  • Oligonucleotides
(all 27)
PubMed
17314132 Full text @ Development
Abstract
Inca (induced in neural crest by AP2) is a novel protein discovered in a microarray screen for genes that are upregulated in Xenopus embryos by the transcriptional activator protein Tfap2a. It has no significant similarity to any known protein, but is conserved among vertebrates. In Xenopus, zebrafish and mouse embryos, Inca is expressed predominantly in the premigratory and migrating neural crest (NC). Knockdown experiments in frog and fish using antisense morpholinos reveal essential functions for Inca in a subset of NC cells that form craniofacial cartilage. Cells lacking Inca migrate successfully but fail to condense into skeletal primordia. Overexpression of Inca disrupts cortical actin and prevents formation of actin 'purse strings', which are required for wound healing in Xenopus embryos. We show that Inca physically interacts with p21-activated kinase 5 (PAK5), a known regulator of the actin cytoskeleton that is co-expressed with Inca in embryonic ectoderm, including in the NC. These results suggest that Inca and PAK5 cooperate in restructuring cytoskeletal organization and in the regulation of cell adhesion in the early embryo and in NC cells during craniofacial development.
Genes / Markers
Figures
Figure Gallery (7 images)
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
ba2TgTransgenic Insertion
    tfap2a_unspecified
      Unspecified
      1 - 2 of 2
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      Human Disease / Model
      No data available
      Sequence Targeting Reagents
      Target Reagent Reagent Type
      inka1aMO1-inka1aMRPHLNO
      1 - 1 of 1
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      Fish
      Antibodies
      No data available
      Orthology
      No data available
      Engineered Foreign Genes
      Marker Marker Type Name
      EGFPEFGEGFP
      1 - 1 of 1
      Show
      Mapping
      No data available