Coupling of Jun amino-terminal kinase and decapentaplegic in Drosophila morphogenesis

被引:181
作者
Glise, B [1 ]
Noselli, S [1 ]
机构
[1] CTR DEV BIOL,UMR 5547 CNRS,F-31062 TOULOUSE,FRANCE
关键词
morphogenesis; hemipterous; TGF-beta; MAPK pathway; cell signaling;
D O I
10.1101/gad.11.13.1738
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dorsal closure in Drosophila embryos involves the migration of two lateral epithelia toward the dorsal midline to establish the dorsal ectoderm. Previous work showed that this morphogenetic movement depends on the activities of a Jun amino (N)-terminal kinase kinase (JNKK) encoded by the hemipterous (hep) gene, and of a JNK encoded by basket. Hep is required for cell determination in the lending edge of migrating epithelia, by controlling specific expression of the puckered (puc) gene in these cells. During dorsal closure, decapentaplegic (dpp), a member of the transforming growth factor-beta (TGF-beta) superfamily, is expressed in the row of cells making up the leading edge of the epithelia. Here, we show that the small GTPases Dcdc42, Drac1, and the Hep JNKK control dpp expression in this migratory process. Appropriate npp and puc expression in the leading edge also depends on the inhibitory function of the puc gene. Further, our data suggest that the leading edge is the source of a JNK autocrine signal, and exclude a role of Dpp as such a ligand. Dorsal closure couples JNK and dpp signaling pathways, a situation that may be conserved in vertebrate development.
引用
收藏
页码:1738 / 1747
页数:10
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