Regulation of Wnt signaling by protein-protein interaction and post-translational modifications

被引:0
作者
Akira Kikuchi
Shosei Kishida
Hideki Yamamoto
机构
[1] Hiroshima University,Department of Biochemistry, Graduate School of Biomedical Sciences
来源
Experimental & Molecular Medicine | 2006年 / 38卷
关键词
β catenin; protein interaction mapping; protein processing; post-translational; TCF transcription factors; Wnt proteins;
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摘要
The Wnt signaling pathway is conserved in various species from worms to mammals, and plays important roles in cellular proliferation, differentiation, and migration. Wnt stabilizes cytoplasmic β-catenin and then the accumulated β-catenin is translocated into the nucleus, where it activates the transcriptional factor T-cell factor (Tcf)/lymphoid enhancer factor (Lef), and thereby stimulates the expression of genes including c-myc, c-jun, fra-1, and cyclin D1. Tight regulation of this response involves post-translational modifications of the components of the Wnt signaling pathway. Phosphorylation, ubiquitination, and sumoylation have been shown to affect the half-life of β-catenin and the transcriptional activity of Tcf/Lef. The precise spatio-temporal patterns of these multiple modifications determine the driving force of various cellular responses.
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页码:1 / 10
页数:9
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