c-fos elimination compensates for disabled-2 requirement in mouse extraembryonic endoderm development

Dong Hua Yang, Elizabeth R. Smith, Kathy Qi Cai, Xiang Xi Michael Xu

    Research output: Contribution to journalArticlepeer-review

    10 Scopus citations

    Abstract

    Disabled-2 (Dab2) is expressed in primitive endoderm cells as they are differentiating from the inner cell mass and dab2 deficiency in mice results in lethality at E5.5-E6.5 due to the disorganization of the endoderm layers. Here we show that Dab2 suppresses c-Fos expression in endoderm cells. A morphological normal primitive endoderm layer was observed in putative E5.5 dab2 (-/-):c-fos (-/-) embryos, indicating that the primitive endoderm defect due to the loss of Dab2 is rescued by deletion of the c-fos gene. The lethality of the double knockout embryos was delayed until E9.5-E10.5 and the defective embryos failed to undergo organogenesis. We conclude that Dab2 plays a role in epithelial organization by suppression of c-Fos expression and suggest that unsuppressed c-Fos can lead to disruption of primitive endoderm epithelial organization, yet an additional dab2 function is required for later organogenesis.

    Original languageEnglish
    Pages (from-to)514-523
    Number of pages10
    JournalDevelopmental Dynamics
    Volume238
    Issue number3
    DOIs
    StatePublished - Mar 2009

    Keywords

    • Adaptor Proteins, Signal Transducing
    • Adaptor Proteins, Vesicular Transport/deficiency
    • Animals
    • Apoptosis Regulatory Proteins
    • Cell Differentiation
    • Down-Regulation
    • Embryo, Mammalian/embryology
    • Embryonic Stem Cells/cytology
    • Endoderm/cytology
    • Gene Deletion
    • Gene Expression Regulation, Developmental
    • Genotype
    • Mice
    • Mice, Knockout
    • Proto-Oncogene Proteins c-fos/deficiency
    • Stem Cells

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