Papers

Peer-reviewed
Mar, 1999

p38 mitogen-activated protein kinase can be involved in transforming growth factor beta superfamily signal transduction in Drosophila wing morphogenesis

MOLECULAR AND CELLULAR BIOLOGY
  • T Adachi-Yamada
  • ,
  • M Nakamura
  • ,
  • K Irie
  • ,
  • Y Tomoyasu
  • ,
  • Y Sano
  • ,
  • E Mori
  • ,
  • S Goto
  • ,
  • N Ueno
  • ,
  • Y Nishida
  • ,
  • K Matsumoto

Volume
19
Number
3
First page
2322
Last page
2329
Language
English
Publishing type
Research paper (scientific journal)
Publisher
AMER SOC MICROBIOLOGY

p38 mitogen-activated protein kinase (p38) has been extensively studied as a stress-responsive kinase, but its role in development remains unknown. The fruit fly, Drosophila melanogaster, has two p38 genes, D-p38a and D-p38b. To elucidate the developmental function of the Drosophila p38's, we used various genetic and pharmacological manipulations to interfere with their functions: expression of a dominant-negative form of D-p38b, expression of antisense D-p38b RNA, reduction of the D-p38 gene dosage, and treatment with the p38 inhibitor SB203580. Expression of a dominant-negative D-p38b in the wing imaginal disc caused a decapentaplegic (dpp)-like phenotype and enhanced the phenotype of a dpp mutant. Dpp is a secretory ligand belonging to the transforming growth factor beta superfamily which triggers various morphogenetic processes through interaction with the receptor Thick veins (Tkv). Inhibition of D-p38b function also caused the suppression of the wing phenotype induced by constitutively active Tkv (Tkv(CA)). Mosaic analysis revealed that D-p38b regulates the Tkv-dependent transcription of the optomotor-blind (omb) gene in non-Dpp-producing cells, indicating that the site of D-p38b action is downstream of Tkv. Furthermore, forced expression of Tkv(CA) induced an increase in the phosphorylated active form(s) of D-p38(s). These results demonstrate that p38, in addition to its role as a transducer of emergency stress signaling, may function to modulate Dpp signaling.

Link information
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000078697900069&DestApp=WOS_CPL
ID information
  • ISSN : 0270-7306
  • Web of Science ID : WOS:000078697900069

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