The SOX family of transcription factors have emerged as modulators of canonical Wnt/beta-catenin signaling in diverse development and disease contexts. There are over 20 SOX proteins encoded in the vertebrate genome and recent evidence suggests that many of these can physically interact with beta-catenin and modulate the transcription of Wnt-target genes. The precise mechanisms by which SOX proteins regulate beta-catenin/TCF activity are still being resolved and there is evidence to support a number of models including: protein-protein interactions, the binding of SOX factors to Wnt-target gene promoters, the recruitment of co-repressors or co-activators, modulation of protein stability, and nuclear translocation. In some contexts, Wnt signaling also regulates SOX expression resulting in feedback regulatory loops that fine-tune cellular responses to beta-catenin/TCF activity. In this review, we summarize the examples of Sox-Wnt interactions and examine the underlying mechanisms of this potentially widespread and underappreciated mode of Wnt-regulation. Developmental Dynamics 239:56-68, 2010. (C) 2009 Wiley-Liss, Inc.
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Stanford Univ, Howard Hughes Med Inst, Dept Dev Biol, Sch Med, Stanford, CA 94305 USAStanford Univ, Howard Hughes Med Inst, Dept Dev Biol, Sch Med, Stanford, CA 94305 USA
机构:Univ Calif San Francisco, Dept Neurol, Program Neurosci, San Francisco, CA 94143 USA
Freese, Jennifer L.
Pino, Darya
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机构:Univ Calif San Francisco, Dept Neurol, Program Neurosci, San Francisco, CA 94143 USA
Pino, Darya
Pleasure, Samuel J.
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Univ Calif San Francisco, Dept Neurol, Program Neurosci, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol, Program Neurosci, San Francisco, CA 94143 USA
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Stanford Univ, Sch Med, Howard Hughes Med Inst, Dept Dev Biol,Beckman Ctr, Stanford, CA 94305 USAStanford Univ, Sch Med, Howard Hughes Med Inst, Dept Dev Biol,Beckman Ctr, Stanford, CA 94305 USA