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Hippo Pathway Phylogenetics Predicts Monoubiquitylation of Salvador and Merlin/Nf2

Recently we employed phylogenetics to predict that the cellular interpretation of TGF-β signals is modulated by monoubiquitylation cycles affecting the Smad4 signal transducer/tumor suppressor. This prediction was subsequently validated by experiments in flies, frogs and mammalian cells. Here we app...

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Detalles Bibliográficos
Autores principales: Wisotzkey, Robert G., Konikoff, Charlotte E., Newfeld, Stuart J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522738/
https://www.ncbi.nlm.nih.gov/pubmed/23272121
http://dx.doi.org/10.1371/journal.pone.0051599
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author Wisotzkey, Robert G.
Konikoff, Charlotte E.
Newfeld, Stuart J.
author_facet Wisotzkey, Robert G.
Konikoff, Charlotte E.
Newfeld, Stuart J.
author_sort Wisotzkey, Robert G.
collection PubMed
description Recently we employed phylogenetics to predict that the cellular interpretation of TGF-β signals is modulated by monoubiquitylation cycles affecting the Smad4 signal transducer/tumor suppressor. This prediction was subsequently validated by experiments in flies, frogs and mammalian cells. Here we apply a phylogenetic approach to the Hippo pathway and predict that two of its signal transducers, Salvador and Merlin/Nf2 (also a tumor suppressor) are regulated by monoubiquitylation. This regulatory mechanism does not lead to protein degradation but instead serves as a highly efficient “off/on” switch when the protein is subsequently deubiquitylated. Overall, our study shows that the creative application of phylogenetics can predict new roles for pathway components and new mechanisms for regulating intercellular signaling pathways.
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spelling pubmed-35227382012-12-27 Hippo Pathway Phylogenetics Predicts Monoubiquitylation of Salvador and Merlin/Nf2 Wisotzkey, Robert G. Konikoff, Charlotte E. Newfeld, Stuart J. PLoS One Research Article Recently we employed phylogenetics to predict that the cellular interpretation of TGF-β signals is modulated by monoubiquitylation cycles affecting the Smad4 signal transducer/tumor suppressor. This prediction was subsequently validated by experiments in flies, frogs and mammalian cells. Here we apply a phylogenetic approach to the Hippo pathway and predict that two of its signal transducers, Salvador and Merlin/Nf2 (also a tumor suppressor) are regulated by monoubiquitylation. This regulatory mechanism does not lead to protein degradation but instead serves as a highly efficient “off/on” switch when the protein is subsequently deubiquitylated. Overall, our study shows that the creative application of phylogenetics can predict new roles for pathway components and new mechanisms for regulating intercellular signaling pathways. Public Library of Science 2012-12-14 /pmc/articles/PMC3522738/ /pubmed/23272121 http://dx.doi.org/10.1371/journal.pone.0051599 Text en © 2012 Wisotzkey et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wisotzkey, Robert G.
Konikoff, Charlotte E.
Newfeld, Stuart J.
Hippo Pathway Phylogenetics Predicts Monoubiquitylation of Salvador and Merlin/Nf2
title Hippo Pathway Phylogenetics Predicts Monoubiquitylation of Salvador and Merlin/Nf2
title_full Hippo Pathway Phylogenetics Predicts Monoubiquitylation of Salvador and Merlin/Nf2
title_fullStr Hippo Pathway Phylogenetics Predicts Monoubiquitylation of Salvador and Merlin/Nf2
title_full_unstemmed Hippo Pathway Phylogenetics Predicts Monoubiquitylation of Salvador and Merlin/Nf2
title_short Hippo Pathway Phylogenetics Predicts Monoubiquitylation of Salvador and Merlin/Nf2
title_sort hippo pathway phylogenetics predicts monoubiquitylation of salvador and merlin/nf2
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522738/
https://www.ncbi.nlm.nih.gov/pubmed/23272121
http://dx.doi.org/10.1371/journal.pone.0051599
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