CKA, a novel multidomain protein, regulates the JUN N-terminal kinase signal transduction pathway in Drosophila

被引:61
作者
Chen, HW
Marinissen, MJ
Oh, SW
Chen, X
Melnick, M
Perrimon, N
Gutkind, JS
Hou, SX
机构
[1] NCI, FCRDC, Immunol Lab, NIH, Frederick, MD 21702 USA
[2] New England Biolabs Inc, Lab Cell Signaling, Beverly, MA 01915 USA
[3] Natl Inst Dent & Craniofacial Res, Oral & Pharyngeal Canc Branch, NIH, Bethesda, MD 20892 USA
[4] Harvard Univ, Sch Med, Howard Hughes Med Inst, Dept Genet, Boston, MA 02115 USA
关键词
D O I
10.1128/MCB.22.6.1792-1803.2002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Drosophila melanogaster JUN N-terminal kinase (DJNK) and DPP (decapentaplegic) signal transduction pathways coordinately regulate epithelial cell sheet movement during the process of dorsal closure in the embryo. By a genetic screen of mutations affecting dorsal closure in Drosophila, we have now identified a multidomain protein, connector of kinase to AP-1 (cka), that functions in the DJNK pathway and controls the localized expression of dpp in the leading-edge cells. We have also investigated how CKA acts. This unique molecule forms a complex with HEP (DJNKK), BSK (DJNK), DJUN, and DFOS. Complex formation activates BSK kinase, which in turn phosphorylates and activates DJUN and DFOS. These data suggest that CKA represents a novel molecule regulating AP-1 activity by organizing a molecular complex of kinases and transcription factors, thus coordinating the spatial-temporal expression of AP-1-regulated genes.
引用
收藏
页码:1792 / 1803
页数:12
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