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Vol. 10, Issue 4, 1119-1131, April 1999

beta -Catenin Can Be Transported into the Nucleus in a Ran-unassisted Manner

Fumihiko Yokoya,* Naoko Imamoto,* Taro Tachibana, and Yoshihiro Yonedadagger

Department of Anatomy and Cell Biology, Osaka University Medical School, Osaka 565-0871, Japan

The nuclear accumulation of beta -catenin plays an important role in the Wingless/Wnt signaling pathway. This study describes an examination of the nuclear import of beta -catenin in living mammalian cells and in vitro semi-intact cells. When injected into the cell cytoplasm, beta -catenin rapidly migrated into the nucleus in a temperature-dependent and wheat germ agglutinin-sensitive manner. In the cell-free import assay, beta -catenin rapidly migrates into the nucleus without the exogenous addition of cytosol, Ran, or ATP/GTP. Cytoplasmic injection of mutant Ran defective in its GTP hydrolysis did not prevent beta -catenin import. Studies using tsBN2, a temperature-sensitive mutant cell line that possesses a point mutation in the RCC1 gene, showed that the import of beta -catenin is insensitive to nuclear Ran-GTP depletion. These results show that beta -catenin possesses the ability to constitutively translocate through the nuclear pores in a manner similar to importin beta  in a Ran-unassisted manner. We further showed that beta -catenin also rapidly exits the nucleus in homokaryons, suggesting that the regulation of nuclear levels of beta -catenin involves both nuclear import and export of this molecule.


*   These authors contributed equally to this work.
dagger    Corresponding author. E-mail address: yyoneda{at}anat3.med.osaka-u.ac.jp.


Molecular Biology of the Cell
Vol. 10, 1119-1131, April 1999
Copyright © 1999 by The American Society for Cell Biology



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