Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2008-2-18
pubmed:abstractText
A key effector of the canonical Wnt pathway is beta-catenin, which binds to TCF/LEF factors to promote the transcription of Wnt target genes. In the absence of Wnt stimulation, beta-catenin is phosphorylated constitutively, and modified with K48-linked ubiquitin for subsequent proteasomal degradation. Here, we identify Trabid as a new positive regulator of Wnt signaling in mammalian and Drosophila cells. Trabid show a remarkable preference for binding to K63-linked ubiquitin chains with its three tandem NZF fingers (Npl4 zinc finger), and it cleaves these chains with its OTU (ovarian tumor) domain. These activities of Trabid are required for efficient TCF-mediated transcription in cells with high Wnt pathway activity, including colorectal cancer cell lines. We further show that Trabid can bind to and deubiquitylate the APC tumor suppressor protein, a negative regulator of Wnt-mediated transcription. Epistasis experiments indicate that Trabid acts below the stabilization of beta-catenin, and that it may affect the association or activity of the TCF-beta-catenin transcription complex. Our results indicate a role of K63-linked ubiquitin chains during Wnt-induced transcription.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18281465-10089881, http://linkedlifedata.com/resource/pubmed/commentcorrection/18281465-10092233, http://linkedlifedata.com/resource/pubmed/commentcorrection/18281465-10228155, http://linkedlifedata.com/resource/pubmed/commentcorrection/18281465-10364252, http://linkedlifedata.com/resource/pubmed/commentcorrection/18281465-10594348, http://linkedlifedata.com/resource/pubmed/commentcorrection/18281465-10664582, http://linkedlifedata.com/resource/pubmed/commentcorrection/18281465-10769018, http://linkedlifedata.com/resource/pubmed/commentcorrection/18281465-10775268, http://linkedlifedata.com/resource/pubmed/commentcorrection/18281465-10921899, http://linkedlifedata.com/resource/pubmed/commentcorrection/18281465-10947987, http://linkedlifedata.com/resource/pubmed/commentcorrection/18281465-10984057, http://linkedlifedata.com/resource/pubmed/commentcorrection/18281465-11007767, 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pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Lef1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Lymphoid Enhancer-Binding Factor 1, http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa B, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/TCF Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin, http://linkedlifedata.com/resource/pubmed/chemical/Wnt Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Wnt1 Protein, http://linkedlifedata.com/resource/pubmed/chemical/beta Catenin, http://linkedlifedata.com/resource/pubmed/chemical/wg protein, Drosophila
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0890-9369
pubmed:author
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