Negative regulation of Caenorhabditis elegans epidermal damage responses by death-associated protein kinase.

نویسندگان

  • Amy Tong
  • Grace Lynn
  • Vy Ngo
  • Daniel Wong
  • Sarah L Moseley
  • Jonathan J Ewbank
  • Alexandr Goncharov
  • Yi-Chun Wu
  • Nathalie Pujol
  • Andrew D Chisholm
چکیده

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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عنوان ژورنال:
  • Proceedings of the National Academy of Sciences of the United States of America

دوره 106 5  شماره 

صفحات  -

تاریخ انتشار 2009