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pubmed-article:10375506pubmed:abstractTextXTcf-3 is an HMG box transcription factor that mediates Xenopus dorsal-ventral axis formation. As a Wnt pathway effector, XTcf-3 interacts with beta-catenin and activates the expression of the dorsal organizing gene siamois, while in the absence of beta-catenin, XTcf-3 functions as a transcriptional repressor. We show that XTcf-3 contains amino- and carboxy-terminal repressor domains and have identified a Xenopus member of the C-terminal Binding Protein family of transcriptional co-repressors (XCtBP) as the C-terminal co-repressor. We show that two XCtBP binding sites near the XTcf-3 carboxy-terminus are required for the interaction of XTcf-3 and XCtBP and for the transcriptional repression mediated by the XTcf-3 carboxy-terminal domain. By fusing the GAL4 activation domain to XCtBP we have generated an antimorphic protein, XCtBP/G4A, that activates siamois transcription through an interaction with endogenous XTcf-3. Ectopic expression of XCtBP/G4A demonstrates that XCtBP functions in the regulation of head and notochord development. Our data support a role for XCtBP as a co-repressor throughout Xenopus development and indicate that XCtBP/G4A will be a useful tool in determining how XCtBP functions in various developmental processes.lld:pubmed
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pubmed-article:10375506pubmed:articleTitleXCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development.lld:pubmed
pubmed-article:10375506pubmed:affiliationDepartment of Biochemistry, Howard Hughes Medical Institute, Center for Developmental Biology, University of Washington School of Medicine, Seattle, Washington 98195-7350, USA. kimelman@u.washington.edu.lld:pubmed
pubmed-article:10375506pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10375506pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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