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Regulation of β-catenin function by the IκB kinases
被引:121
作者:
Lamberti, C
Lin, KM
Yamamoto, Y
Verma, U
Verma, IM
Byers, S
Gaynor, RB
机构:
[1] Univ Texas, SW Med Ctr, Dept Med, Div Hematol Oncol,Harold Simmons Canc Ctr, Dallas, TX 75390 USA
[2] Salk Inst Biol Studies, La Jolla, CA 92037 USA
[3] Georgetown Univ, Sch Med, Lombardi Canc Ctr, Dept Cell Biol, Washington, DC 20007 USA
[4] Georgetown Univ, Sch Med, Lombardi Canc Ctr, Dept Oncol, Washington, DC 20007 USA
关键词:
D O I:
10.1074/jbc.M104227200
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:
Both the beta -catenin and the nuclear factor kappaB (NF-kappaB) proteins are important regulators of gene expression and cellular proliferation. Two kinases, IKK alpha and IKK beta, are critical activators of the NF-kappaB pathway. Here we present evidence that these kinases are also important in the regulation of beta -catenin function. IKK alpha- and IKK beta -eficient mouse embryo fibroblasts exhibited different patterns of beta -catenin cellular localization. IKK beta decreases beta -catenin-dependent transcriptional activation, while IKK alpha increases beta -catenin-dependent transcriptional activity. IKK alpha and IKK beta interact with and phosphorylate beta -catenin using both in vitro and in vivo assays. Our results suggest that differential interactions of beta -catenin with IKK alpha and IKK beta may in part be responsible for regulating beta -catenin protein levels and cellular localization and integrating signaling events between the NF-kappaB and Wingless pathways.
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页码:42276 / 42286
页数:11
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