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XB-ART-36867
Mol Cell Biol February 1, 2008; 28 (3): 977-87.

Myeloid translocation gene family members associate with T-cell factors (TCFs) and influence TCF-dependent transcription.

Moore AC , Amann JM , Williams CS , Tahinci E , Farmer TE , Martinez JA , Yang G , Luce KS , Lee E , Hiebert SW .


Abstract
Canonical Wnt signaling is mediated by a molecular "switch" that regulates the transcriptional properties of the T-cell factor (TCF) family of DNA-binding proteins. Members of the myeloid translocation gene (MTG) family of transcriptional corepressors are frequently disrupted by chromosomal translocations in acute myeloid leukemia, whereas MTG16 may be inactivated in up to 40% of breast cancer and MTG8 is a candidate cancer gene in colorectal carcinoma. Genetic studies imply that this corepressor family may function in stem cells. Given that mice lacking Myeloid Translocation Gene Related-1 (Mtgr1) fail to maintain the secretory lineage in the small intestine, we surveyed transcription factors that might recruit Mtgr1 in intestinal stem cells or progenitor cells and found that MTG family members associate specifically with TCF4. Coexpression of beta-catenin disrupted the association between these corepressors and TCF4. Furthermore, when expressed in Xenopus embryos, MTG family members inhibited axis formation and impaired the ability of beta-catenin and XLef-1 to induce axis duplication, indicating that MTG family members act downstream of beta-catenin. Moreover, we found that c-Myc, a transcriptional target of the Wnt pathway, was overexpressed in the small intestines of mice lacking Mtgr1, thus linking inactivation of Mtgr1 to the activation of a potent oncogene.

PubMed ID: 18039847
PMC ID: PMC2223385
Article link: Mol Cell Biol
Grant support: [+]
Genes referenced: cbfa2t2 cbfa2t3 lef1 myc prss3 runx1t1 tcf4

References [+] :
Amann, ETO, a target of t(8;21) in acute leukemia, makes distinct contacts with multiple histone deacetylases and binds mSin3A through its oligomerization domain. 2001, Pubmed


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