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Wnt pathway activation by ADP-ribosylation
Wnt/β-catenin signalling directs fundamental processes during metazoan development and can be aberrantly activated in cancer. Wnt stimulation induces the recruitment of the scaffold protein Axin from an inhibitory destruction complex to a stimulatory signalosome. Here we analyse the early effects of...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857404/ https://www.ncbi.nlm.nih.gov/pubmed/27138857 http://dx.doi.org/10.1038/ncomms11430 |
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author | Yang, Eungi Tacchelly-Benites, Ofelia Wang, Zhenghan Randall, Michael P. Tian, Ai Benchabane, Hassina Freemantle, Sarah Pikielny, Claudio Tolwinski, Nicholas S. Lee, Ethan Ahmed, Yashi |
author_facet | Yang, Eungi Tacchelly-Benites, Ofelia Wang, Zhenghan Randall, Michael P. Tian, Ai Benchabane, Hassina Freemantle, Sarah Pikielny, Claudio Tolwinski, Nicholas S. Lee, Ethan Ahmed, Yashi |
author_sort | Yang, Eungi |
collection | PubMed |
description | Wnt/β-catenin signalling directs fundamental processes during metazoan development and can be aberrantly activated in cancer. Wnt stimulation induces the recruitment of the scaffold protein Axin from an inhibitory destruction complex to a stimulatory signalosome. Here we analyse the early effects of Wnt on Axin and find that the ADP-ribose polymerase Tankyrase (Tnks)—known to target Axin for proteolysis—regulates Axin's rapid transition following Wnt stimulation. We demonstrate that the pool of ADP-ribosylated Axin, which is degraded under basal conditions, increases immediately following Wnt stimulation in both Drosophila and human cells. ADP-ribosylation of Axin enhances its interaction with the Wnt co-receptor LRP6, an essential step in signalosome assembly. We suggest that in addition to controlling Axin levels, Tnks-dependent ADP-ribosylation promotes the reprogramming of Axin following Wnt stimulation; and propose that Tnks inhibition blocks Wnt signalling not only by increasing destruction complex activity, but also by impeding signalosome assembly. |
format | Online Article Text |
id | pubmed-4857404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48574042016-05-23 Wnt pathway activation by ADP-ribosylation Yang, Eungi Tacchelly-Benites, Ofelia Wang, Zhenghan Randall, Michael P. Tian, Ai Benchabane, Hassina Freemantle, Sarah Pikielny, Claudio Tolwinski, Nicholas S. Lee, Ethan Ahmed, Yashi Nat Commun Article Wnt/β-catenin signalling directs fundamental processes during metazoan development and can be aberrantly activated in cancer. Wnt stimulation induces the recruitment of the scaffold protein Axin from an inhibitory destruction complex to a stimulatory signalosome. Here we analyse the early effects of Wnt on Axin and find that the ADP-ribose polymerase Tankyrase (Tnks)—known to target Axin for proteolysis—regulates Axin's rapid transition following Wnt stimulation. We demonstrate that the pool of ADP-ribosylated Axin, which is degraded under basal conditions, increases immediately following Wnt stimulation in both Drosophila and human cells. ADP-ribosylation of Axin enhances its interaction with the Wnt co-receptor LRP6, an essential step in signalosome assembly. We suggest that in addition to controlling Axin levels, Tnks-dependent ADP-ribosylation promotes the reprogramming of Axin following Wnt stimulation; and propose that Tnks inhibition blocks Wnt signalling not only by increasing destruction complex activity, but also by impeding signalosome assembly. Nature Publishing Group 2016-05-03 /pmc/articles/PMC4857404/ /pubmed/27138857 http://dx.doi.org/10.1038/ncomms11430 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yang, Eungi Tacchelly-Benites, Ofelia Wang, Zhenghan Randall, Michael P. Tian, Ai Benchabane, Hassina Freemantle, Sarah Pikielny, Claudio Tolwinski, Nicholas S. Lee, Ethan Ahmed, Yashi Wnt pathway activation by ADP-ribosylation |
title | Wnt pathway activation by ADP-ribosylation |
title_full | Wnt pathway activation by ADP-ribosylation |
title_fullStr | Wnt pathway activation by ADP-ribosylation |
title_full_unstemmed | Wnt pathway activation by ADP-ribosylation |
title_short | Wnt pathway activation by ADP-ribosylation |
title_sort | wnt pathway activation by adp-ribosylation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857404/ https://www.ncbi.nlm.nih.gov/pubmed/27138857 http://dx.doi.org/10.1038/ncomms11430 |
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