Mitotic wnt signaling promotes protein stabilization and regulates cell size.

Mol Cell 2014 May 15;54(4):663-74. Epub 2014 May 15.

DKFZ-ZMBH Alliance, Division of Molecular Embryology, DKFZ, Im Neuenheimer Feld 280, D-69120 Heidelberg, Germany; Institute of Molecular Biology, Ackermannweg 4, D-55128 Mainz, Germany. Electronic address:

Canonical Wnt signaling is thought to regulate cell behavior mainly by inducing β-catenin-dependent transcription of target genes. In proliferating cells Wnt signaling peaks in the G2/M phase of the cell cycle, but the significance of this "mitotic Wnt signaling" is unclear. Here we introduce Wnt-dependent stabilization of proteins (Wnt/STOP), which is independent of β-catenin and peaks during mitosis. We show that Wnt/STOP plays a critical role in protecting proteins, including c-MYC, from GSK3-dependent polyubiquitination and degradation. Wnt/STOP signaling increases cellular protein levels and cell size. Wnt/STOP, rather than β-catenin signaling, is the dominant mode of Wnt signaling in several cancer cell lines, where it is required for cell growth. We propose that Wnt/STOP signaling slows down protein degradation as cells prepare to divide.

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http://dx.doi.org/10.1016/j.molcel.2014.04.014DOI Listing
May 2014
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