Negative regulation of Caenorhabditis elegans epidermal damage responses by death-associated protein kinase
Author(s) -
Amy H.Y. Tong,
Grace Lynn,
Vy Ngo,
Daniel Wong,
Sarah Moseley,
Jonathan J. Ewbank,
Alexandr Goncharov,
YiChun Wu,
Nathalie Pujol,
Andrew Chisholm
Publication year - 2009
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0809339106
Subject(s) - caenorhabditis elegans , innate immune system , biology , microbiology and biotechnology , immune system , signal transduction , protein kinase a , kinase , suppressor , regulator , immunology , genetics , gene
Wounding of epidermal layers triggers multiple coordinated responses to damage. We show here that the Caenorhabditis elegans ortholog of the tumor suppressor death-associated protein kinase, dapk-1, acts as a previously undescribed negative regulator of barrier repair and innate immune responses to wounding. Loss of DAPK-1 function results in constitutive formation of scar-like structures in the cuticle, and up-regulation of innate immune responses to damage. Overexpression of DAPK-1 represses innate immune responses to needle wounding. Up-regulation of innate immune responses in dapk-1 requires the TIR-1/p38 signal transduction pathway; loss of function in this pathway synergizes with dapk-1 to drastically reduce adult lifespan. Our results reveal a previously undescribed function for the DAPK tumor suppressor family in regulation of epithelial damage responses.
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