Tissue-specific derepression of TCF/LEF controls the activity of the Wnt/β-catenin pathway

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作者
Fu-I Lu
Yong-Hua Sun
Chang-Yong Wei
Christine Thisse
Bernard Thisse
机构
[1] University of Virginia,Department of Cell Biology
[2] Institute of Biotechnology,undefined
[3] National Cheng Kung University,undefined
[4] Institut de Génétique et de Biologie Moléculaire et Cellulaire,undefined
[5] CNRS/INSERM/Université de Strasbourg,undefined
[6] State Key Laboratory of Freshwater Ecology and Biotechnology,undefined
[7] Institute of Hydrobiology,undefined
[8] Chinese Academy of Sciences,undefined
[9] University of Chinese Academy of Sciences,undefined
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Upon stimulation by Wnt ligands, the canonical Wnt/β-catenin signalling pathway results in the stabilization of β-catenin and its translocation into the nucleus to form transcriptionally active complexes with sequence-specific DNA-binding T-cell factor/lymphoid enhancer factor (TCF/LEF) family proteins. In the absence of nuclear β-catenin, TCF proteins act as transcriptional repressors by binding to Groucho/Transducin-Like Enhancer of split (TLE) proteins that function as co-repressors by interacting with histone deacetylases whose activity leads to the generation of transcriptionally silent chromatin. Here we show that the transcription factor Ladybird homeobox 2 (Lbx2) positively controls the Wnt/β-catenin signalling pathway in the posterior lateral and ventral mesoderm of the zebrafish embryo at the gastrula stage, by directly interfering with the binding of Groucho/TLE to TCF, thereby preventing formation of transcription repressor complexes. These findings reveal a novel level of regulation of the canonical Wnt/β-catenin signalling pathway occurring in the nucleus and involving tissue-specific derepression of TCF by Lbx2.
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