Article ID Journal Published Year Pages File Type
10904926 Experimental Cell Research 2005 7 Pages PDF
Abstract
Nuclear accumulation of β-catenin plays an important role in the Wnt signaling pathway. In the nucleus, β-catenin acts as a transcriptional co-activator for TCF/LEF family of transcription factors. It has been shown that lef-1 contains a typical basic type nuclear localization signal (NLS) and is transported into the nucleus by the conventional import pathway. In this study, we found that a mutant lef-1 lacking the classical NLS accumulated in the nucleus of living cells, when β-catenin was co-expressed. In addition, in a cell-free import assay, lef-1 migrated into the nucleus in the presence of β-catenin alone without any other soluble factors. In contrast, another mutant lef-1 lacking the β-catenin binding domain failed to migrate into the nucleus, even in the presence of β-catenin. These findings indicate that β-catenin alone can mediate the nuclear import of lef-1 through the direct binding. Collectively, we propose that there are two distinct pathways for the nuclear import of lef-1: importin α/β-mediated and β-catenin-mediated one, which provides a novel paradigm for Wnt signaling pathway.
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