The β-catenin HMP-2 functions downstream of Src in parallel with the Wnt pathway in early embryogenesis of C. elegans

Eisuke Sumiyoshi, Sachiko Takahashi, Hatsue Obata, Asako Sugimoto, Yuji Kohara

    Research output: Contribution to journalArticlepeer-review

    15 Citations (Scopus)

    Abstract

    The Wnt and Src pathways are widely used signal transduction pathways in development. β-catenin is utilized in both pathways, as a signal transducer and a component of the cadherin cell adhesion complex, respectively. A C. elegans β-catenin HMP-2 is involved in cell adhesion, but its signaling role has been unknown. Here, we report that in early embryogenesis HMP-2 acts as a signaling molecule in the Src signal. During early embryogenesis in C. elegans, the Wnt and Src pathways are redundantly involved in endoderm induction at the four-cell stage and spindle orientation in an ABar blastomere. RNAi experiments demonstrated that HMP-2 functions in the Src pathway, but in parallel with the Wnt pathway in these processes. HMP-2 localized at the cell boundaries and nuclei, and its localization at cell boundaries was negatively regulated by SRC-1. In addition, HMP-2 was Tyr-phosphorylated in a SRC-1-dependent manner in vivo. Taken together, we propose that HMP-2 functions downstream of the Src signaling pathway and contribute to endoderm induction and ABar spindle orientation, in parallel with the Wnt signaling pathway.

    Original languageEnglish
    Pages (from-to)302-312
    Number of pages11
    JournalDevelopmental Biology
    Volume355
    Issue number2
    DOIs
    Publication statusPublished - 2011 Jul 15

    Keywords

    • C. elegans
    • Endoderm induction
    • Src signal
    • Wnt signal
    • β-catenin

    ASJC Scopus subject areas

    • Molecular Biology
    • Developmental Biology
    • Cell Biology

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