| Literature DB >> 10898789 |
K Tago1, T Nakamura, M Nishita, J Hyodo, S Nagai, Y Murata, S Adachi, S Ohwada, Y Morishita, H Shibuya, T Akiyama.
Abstract
Wnt signaling has an important role in both embryonic development and tumorigenesis. beta-Catenin, a key component of the Wnt signaling pathway, interacts with the TCF/LEF family of transcription factors and activates transcription of Wnt target genes. Here, we identify a novel beta-catenin-interacting protein, ICAT, that was found to inhibit the interaction of beta-catenin with TCF-4 and represses beta-catenin-TCF-4-mediated transactivation. Furthermore, ICAT inhibited Xenopus axis formation by interfering with Wnt signaling. These results suggest that ICAT negatively regulates Wnt signaling via inhibition of the interaction between beta-catenin and TCF and is integral in development and cell proliferation.Entities:
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Year: 2000 PMID: 10898789 PMCID: PMC316784
Source DB: PubMed Journal: Genes Dev ISSN: 0890-9369 Impact factor: 11.361