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Destruction complex dynamics: Wnt/?-catenin signaling alters Axin-GSK3? interactions in vivo.


ABSTRACT: The central regulator of the Wnt/?-catenin pathway is the Axin/APC/GSK3? destruction complex (DC), which, under unstimulated conditions, targets cytoplasmic ?-catenin for degradation. How Wnt activation inhibits the DC to permit ?-catenin-dependent signaling remains controversial, in part because the DC and its regulation have never been observed in vivo Using bimolecular fluorescence complementation (BiFC) methods, we have now analyzed the activity of the DC under near-physiological conditions in Drosophila By focusing on well-established patterns of Wnt/Wg signaling in the developing Drosophila wing, we have defined the sequence of events by which activated Wnt receptors induce a conformational change within the DC, resulting in modified Axin-GSK3? interactions that prevent ?-catenin degradation. Surprisingly, the nucleus is surrounded by active DCs, which principally control the degradation of ?-catenin and thereby nuclear access. These DCs are inactivated and removed upon Wnt signal transduction. These results suggest a novel mechanistic model for dynamic Wnt signal transduction in vivo.

SUBMITTER: Lybrand DB 

PROVIDER: S-EPMC6633605 | biostudies-literature | 2019 Jul

REPOSITORIES: biostudies-literature

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Destruction complex dynamics: Wnt/β-catenin signaling alters Axin-GSK3β interactions <i>in vivo</i>.

Lybrand Daniel B DB   Naiman Misha M   Laumann Jessie May JM   Boardman Mitzi M   Petshow Samuel S   Hansen Kevin K   Scott Gregory G   Wehrli Marcel M  

Development (Cambridge, England) 20190702 13


The central regulator of the Wnt/β-catenin pathway is the Axin/APC/GSK3β destruction complex (DC), which, under unstimulated conditions, targets cytoplasmic β-catenin for degradation. How Wnt activation inhibits the DC to permit β-catenin-dependent signaling remains controversial, in part because the DC and its regulation have never been observed <i>in vivo</i> Using bimolecular fluorescence complementation (BiFC) methods, we have now analyzed the activity of the DC under near-physiological cond  ...[more]

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