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Signalling activity of β-catenin targeted to different subcellular compartments

Signalling activity of β-catenin targeted to different subcellular compartments
Signalling activity of β-catenin targeted to different subcellular compartments

β-Catenin plays a dual role as an adhesion molecule in adherens junctions at the plasma membrane and as a key intermediate in the canonical Wnt signalling pathway. The cytosolic soluble pool of β-catenin, involved in the transmission of the Wnt signal, is normally subjected to rapid protein degradation. On activation of the Wnt cascade, β-catenin becomes stabilized and then translocates into the nucleus where it co-activates transcription factors of the TCF (T-cell factor)/LEF (lymphoid enhancer factor) family. The expression of plasma membrane-targeted forms of β-catenin has been shown to also activate TCF/LEF-dependent transcription and different mechanisms have been put forward. In the present study, we have undertaken a systematic analysis of the signalling capability of non-degradable forms of β-catenin targeted to different cellular compartments. β-Catenin targeted to the plasma membrane activated transcription to a greater extent compared with non-targeted β-catenin, and led to a marked stabilization of cytosolic soluble β-catenin. These effects were independent of the competition with endogenous β-catenin for binding to E-cadherin at the plasma membrane, since targeting non-degradable β-catenin to other cellular compartments, i.e. the outer mitochondrial membrane and the endoplasmic reticulum membrane, also resulted in the accumulation of cytosolic wildtype β-catenin and activation of β-catenin-dependent signalling. In contrast, nuclear-targeted β-catenin was without significant effect on cytosolic wild-type β-catenin and did not activate transcription. Our results suggest that cytosolic accumulation of β-catenin is a prerequisite for the activation of TCF/LEF-dependent transcription in the nucleus.

β-catenin, Subcellular localization, Transcriptional activity, Wnt signalling
0264-6021
471-477
Hagen, Thilo
9e5b7a99-1eb6-4e3c-8aa7-ffe728fa189d
Sethi, Jaswinder K.
923f1a81-91e4-46cd-8853-bb4a979f5a85
Foxwell, Neale
49c9c573-d0f1-412c-a7dc-1148b24333d0
Vidal-Puig, Antonio
7d46d380-1b9d-40cb-90a3-72679e143036
Hagen, Thilo
9e5b7a99-1eb6-4e3c-8aa7-ffe728fa189d
Sethi, Jaswinder K.
923f1a81-91e4-46cd-8853-bb4a979f5a85
Foxwell, Neale
49c9c573-d0f1-412c-a7dc-1148b24333d0
Vidal-Puig, Antonio
7d46d380-1b9d-40cb-90a3-72679e143036

Hagen, Thilo, Sethi, Jaswinder K., Foxwell, Neale and Vidal-Puig, Antonio (2004) Signalling activity of β-catenin targeted to different subcellular compartments. Biochemical Journal, 379 (2), 471-477. (doi:10.1042/BJ20031749).

Record type: Article

Abstract

β-Catenin plays a dual role as an adhesion molecule in adherens junctions at the plasma membrane and as a key intermediate in the canonical Wnt signalling pathway. The cytosolic soluble pool of β-catenin, involved in the transmission of the Wnt signal, is normally subjected to rapid protein degradation. On activation of the Wnt cascade, β-catenin becomes stabilized and then translocates into the nucleus where it co-activates transcription factors of the TCF (T-cell factor)/LEF (lymphoid enhancer factor) family. The expression of plasma membrane-targeted forms of β-catenin has been shown to also activate TCF/LEF-dependent transcription and different mechanisms have been put forward. In the present study, we have undertaken a systematic analysis of the signalling capability of non-degradable forms of β-catenin targeted to different cellular compartments. β-Catenin targeted to the plasma membrane activated transcription to a greater extent compared with non-targeted β-catenin, and led to a marked stabilization of cytosolic soluble β-catenin. These effects were independent of the competition with endogenous β-catenin for binding to E-cadherin at the plasma membrane, since targeting non-degradable β-catenin to other cellular compartments, i.e. the outer mitochondrial membrane and the endoplasmic reticulum membrane, also resulted in the accumulation of cytosolic wildtype β-catenin and activation of β-catenin-dependent signalling. In contrast, nuclear-targeted β-catenin was without significant effect on cytosolic wild-type β-catenin and did not activate transcription. Our results suggest that cytosolic accumulation of β-catenin is a prerequisite for the activation of TCF/LEF-dependent transcription in the nucleus.

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More information

e-pub ahead of print date: 15 April 2004
Published date: 15 April 2004
Keywords: β-catenin, Subcellular localization, Transcriptional activity, Wnt signalling

Identifiers

Local EPrints ID: 415407
URI: http://eprints.soton.ac.uk/id/eprint/415407
ISSN: 0264-6021
PURE UUID: 76ddd93a-17f8-40d3-9560-b62844a1b6a1
ORCID for Jaswinder K. Sethi: ORCID iD orcid.org/0000-0003-4157-0475

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Date deposited: 09 Nov 2017 17:30
Last modified: 16 Mar 2024 04:31

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Contributors

Author: Thilo Hagen
Author: Neale Foxwell
Author: Antonio Vidal-Puig

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