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USP42 protects ZNRF3/RNF43 from R‐spondin‐dependent clearance and inhibits Wnt signalling
The tumour suppressors RNF43 and ZNRF3 play a central role in development and tissue homeostasis by promoting the turnover of the Wnt receptors LRP6 and Frizzled (FZD). The stem cell growth factor R‐spondin induces auto‐ubiquitination and membrane clearance of ZNRF3/RNF43 to promote Wnt signalling....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097334/ https://www.ncbi.nlm.nih.gov/pubmed/33786993 http://dx.doi.org/10.15252/embr.202051415 |
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author | Giebel, Nicole de Jaime‐Soguero, Anchel García del Arco, Ana Landry, Jonathan J M Tietje, Marlene Villacorta, Laura Benes, Vladimir Fernández‐Sáiz, Vanesa Acebrón, Sergio P |
author_facet | Giebel, Nicole de Jaime‐Soguero, Anchel García del Arco, Ana Landry, Jonathan J M Tietje, Marlene Villacorta, Laura Benes, Vladimir Fernández‐Sáiz, Vanesa Acebrón, Sergio P |
author_sort | Giebel, Nicole |
collection | PubMed |
description | The tumour suppressors RNF43 and ZNRF3 play a central role in development and tissue homeostasis by promoting the turnover of the Wnt receptors LRP6 and Frizzled (FZD). The stem cell growth factor R‐spondin induces auto‐ubiquitination and membrane clearance of ZNRF3/RNF43 to promote Wnt signalling. However, the deubiquitinase stabilising ZNRF3/RNF43 at the plasma membrane remains unknown. Here, we show that the USP42 antagonises R‐spondin by protecting ZNRF3/RNF43 from ubiquitin‐dependent clearance. USP42 binds to the Dishevelled interacting region (DIR) of ZNRF3 and stalls the R‐spondin‐LGR4‐ZNRF3 ternary complex by deubiquitinating ZNRF3. Accordingly, USP42 increases the turnover of LRP6 and Frizzled (FZD) receptors and inhibits Wnt signalling. Furthermore, we show that USP42 functions as a roadblock for paracrine Wnt signalling in colon cancer cells and mouse small intestinal organoids. We provide new mechanistic insights into the regulation R‐spondin and conclude that USP42 is crucial for ZNRF3/RNF43 stabilisation at the cell surface. |
format | Online Article Text |
id | pubmed-8097334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80973342021-05-14 USP42 protects ZNRF3/RNF43 from R‐spondin‐dependent clearance and inhibits Wnt signalling Giebel, Nicole de Jaime‐Soguero, Anchel García del Arco, Ana Landry, Jonathan J M Tietje, Marlene Villacorta, Laura Benes, Vladimir Fernández‐Sáiz, Vanesa Acebrón, Sergio P EMBO Rep Articles The tumour suppressors RNF43 and ZNRF3 play a central role in development and tissue homeostasis by promoting the turnover of the Wnt receptors LRP6 and Frizzled (FZD). The stem cell growth factor R‐spondin induces auto‐ubiquitination and membrane clearance of ZNRF3/RNF43 to promote Wnt signalling. However, the deubiquitinase stabilising ZNRF3/RNF43 at the plasma membrane remains unknown. Here, we show that the USP42 antagonises R‐spondin by protecting ZNRF3/RNF43 from ubiquitin‐dependent clearance. USP42 binds to the Dishevelled interacting region (DIR) of ZNRF3 and stalls the R‐spondin‐LGR4‐ZNRF3 ternary complex by deubiquitinating ZNRF3. Accordingly, USP42 increases the turnover of LRP6 and Frizzled (FZD) receptors and inhibits Wnt signalling. Furthermore, we show that USP42 functions as a roadblock for paracrine Wnt signalling in colon cancer cells and mouse small intestinal organoids. We provide new mechanistic insights into the regulation R‐spondin and conclude that USP42 is crucial for ZNRF3/RNF43 stabilisation at the cell surface. John Wiley and Sons Inc. 2021-03-30 2021-05-05 /pmc/articles/PMC8097334/ /pubmed/33786993 http://dx.doi.org/10.15252/embr.202051415 Text en © 2021 The Authors. Published under the terms of the CC BY NC ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Articles Giebel, Nicole de Jaime‐Soguero, Anchel García del Arco, Ana Landry, Jonathan J M Tietje, Marlene Villacorta, Laura Benes, Vladimir Fernández‐Sáiz, Vanesa Acebrón, Sergio P USP42 protects ZNRF3/RNF43 from R‐spondin‐dependent clearance and inhibits Wnt signalling |
title | USP42 protects ZNRF3/RNF43 from R‐spondin‐dependent clearance and inhibits Wnt signalling |
title_full | USP42 protects ZNRF3/RNF43 from R‐spondin‐dependent clearance and inhibits Wnt signalling |
title_fullStr | USP42 protects ZNRF3/RNF43 from R‐spondin‐dependent clearance and inhibits Wnt signalling |
title_full_unstemmed | USP42 protects ZNRF3/RNF43 from R‐spondin‐dependent clearance and inhibits Wnt signalling |
title_short | USP42 protects ZNRF3/RNF43 from R‐spondin‐dependent clearance and inhibits Wnt signalling |
title_sort | usp42 protects znrf3/rnf43 from r‐spondin‐dependent clearance and inhibits wnt signalling |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097334/ https://www.ncbi.nlm.nih.gov/pubmed/33786993 http://dx.doi.org/10.15252/embr.202051415 |
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