FB2024_03 , released June 25, 2024
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Citation
Kadrmas, J.L., Smith, M.A., Clark, K.A., Pronovost, S.M., Muster, N., Yates, J.R., Beckerle, M.C. (2004). The integrin effector PINCH regulates JNK activity and epithelial migration in concert with Ras suppressor 1.  J. Cell Biol. 167(6): 1019--1024.
FlyBase ID
FBrf0184059
Publication Type
Research paper
Abstract
Cell adhesion and migration are dynamic processes requiring the coordinated action of multiple signaling pathways, but the mechanisms underlying signal integration have remained elusive. Drosophila embryonic dorsal closure (DC) requires both integrin function and c-Jun amino-terminal kinase (JNK) signaling for opposed epithelial sheets to migrate, meet, and suture. Here, we show that PINCH, a protein required for integrin-dependent cell adhesion and actin-membrane anchorage, is present at the leading edge of these migrating epithelia and is required for DC. By analysis of native protein complexes, we identify RSU-1, a regulator of Ras signaling in mammalian cells, as a novel PINCH binding partner that contributes to PINCH stability. Mutation of the gene encoding RSU-1 results in wing blistering in Drosophila, demonstrating its role in integrin-dependent cell adhesion. Genetic interaction analyses reveal that both PINCH and RSU-1 antagonize JNK signaling during DC. Our results suggest that PINCH and RSU-1 contribute to the integration of JNK and integrin functions during Drosophila development.
PubMed ID
PubMed Central ID
PMC2034365 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    J. Cell Biol.
    Title
    Journal of Cell Biology
    Publication Year
    1966-
    ISBN/ISSN
    0021-9525
    Data From Reference
    Aberrations (1)
    Alleles (9)
    Genes (9)
    Physical Interactions (12)
    Cell Lines (1)
    Insertions (2)
    Transgenic Constructs (2)