TCF/LEFs and Wnt Signaling in the Nucleus

被引:492
|
作者
Cadigan, Ken M. [2 ]
Waterman, Marian L. [1 ]
机构
[1] Univ Calif Irvine, Dept Microbiol & Mol Genet, Irvine, CA 92697 USA
[2] Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
来源
基金
美国国家科学基金会;
关键词
T-CELL-FACTOR; VITAMIN-D-RECEPTOR; TERMINAL-BINDING-PROTEIN; NCK-INTERACTING KINASE; BETA-CATENIN MUTATIONS; ANDROGEN-RECEPTOR; WNT/BETA-CATENIN; TRANSCRIPTION FACTOR; PROSTATE-CANCER; TUMOR-SUPPRESSOR;
D O I
10.1101/cshperspect.a007906
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
T-cell factor/lymphoid enhancer factor (TCF/LEF) transcription factors are the major end point mediators of Wnt/Wingless signaling throughout metazoans. TCF/LEFs are multifunctional proteins that use their sequence-specific DNA-binding and context-dependent interactions to specify which genes will be regulated by Wnts. Much of the work to define their actions has focused on their ability to repress target gene expression when Wnt signals are absent and to recruit beta-catenin to target genes for activation when Wnts are present. Recent advances have highlighted how these on/off actions are regulated by Wnt signals and stabilized beta-catenin. In contrast to invertebrates, which typically contain one TCF/LEF protein that can both activate and repress Wnt targets, gene duplication and isoform complexity of the family in vertebrates have led to specialization, in which individual TCF/LEF isoforms have distinct activities.
引用
收藏
页数:22
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