Abstract:
: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.
journal_name
Mol Celljournal_title
Molecular cellauthors
Acebron SP,Karaulanov E,Berger BS,Huang YL,Niehrs Cdoi
10.1016/j.molcel.2014.04.014subject
Has Abstractpub_date
2014-05-22 00:00:00pages
663-74issue
4eissn
1097-2765issn
1097-4164pii
S1097-2765(14)00325-6journal_volume
54pub_type
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