Cargando…

Wnt ligand–dependent activation of the negative feedback regulator Nkd1

Misregulation of Wnt signaling is at the root of many diseases, most notably colorectal cancer, and although we understand the activation of the pathway, we have a very poor understanding of the circumstances under which Wnt signaling turns itself off. There are numerous negative feedback regulators...

Descripción completa

Detalles Bibliográficos
Autores principales: Larraguibel, Jahdiel, Weiss, Alexander R. E., Pasula, Daniel J., Dhaliwal, Rasmeet S., Kondra, Roman, Van Raay, Terence J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462952/
https://www.ncbi.nlm.nih.gov/pubmed/25904337
http://dx.doi.org/10.1091/mbc.E14-12-1648
_version_ 1782375741205250048
author Larraguibel, Jahdiel
Weiss, Alexander R. E.
Pasula, Daniel J.
Dhaliwal, Rasmeet S.
Kondra, Roman
Van Raay, Terence J.
author_facet Larraguibel, Jahdiel
Weiss, Alexander R. E.
Pasula, Daniel J.
Dhaliwal, Rasmeet S.
Kondra, Roman
Van Raay, Terence J.
author_sort Larraguibel, Jahdiel
collection PubMed
description Misregulation of Wnt signaling is at the root of many diseases, most notably colorectal cancer, and although we understand the activation of the pathway, we have a very poor understanding of the circumstances under which Wnt signaling turns itself off. There are numerous negative feedback regulators of Wnt signaling, but two stand out as constitutive and obligate Wnt-induced regulators: Axin2 and Nkd1. Whereas Axin2 behaves similarly to Axin in the destruction complex, Nkd1 is more enigmatic. Here we use zebrafish blastula cells that are responsive Wnt signaling to demonstrate that Nkd1 activity is specifically dependent on Wnt ligand activation of the receptor. Furthermore, our results support the hypothesis that Nkd1 is recruited to the Wnt signalosome with Dvl2, where it becomes activated to move into the cytoplasm to interact with β-catenin, inhibiting its nuclear accumulation. Comparison of these results with Nkd function in Drosophila generates a unified and conserved model for the role of this negative feedback regulator in the modulation of Wnt signaling.
format Online
Article
Text
id pubmed-4462952
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher The American Society for Cell Biology
record_format MEDLINE/PubMed
spelling pubmed-44629522015-08-30 Wnt ligand–dependent activation of the negative feedback regulator Nkd1 Larraguibel, Jahdiel Weiss, Alexander R. E. Pasula, Daniel J. Dhaliwal, Rasmeet S. Kondra, Roman Van Raay, Terence J. Mol Biol Cell Articles Misregulation of Wnt signaling is at the root of many diseases, most notably colorectal cancer, and although we understand the activation of the pathway, we have a very poor understanding of the circumstances under which Wnt signaling turns itself off. There are numerous negative feedback regulators of Wnt signaling, but two stand out as constitutive and obligate Wnt-induced regulators: Axin2 and Nkd1. Whereas Axin2 behaves similarly to Axin in the destruction complex, Nkd1 is more enigmatic. Here we use zebrafish blastula cells that are responsive Wnt signaling to demonstrate that Nkd1 activity is specifically dependent on Wnt ligand activation of the receptor. Furthermore, our results support the hypothesis that Nkd1 is recruited to the Wnt signalosome with Dvl2, where it becomes activated to move into the cytoplasm to interact with β-catenin, inhibiting its nuclear accumulation. Comparison of these results with Nkd function in Drosophila generates a unified and conserved model for the role of this negative feedback regulator in the modulation of Wnt signaling. The American Society for Cell Biology 2015-06-15 /pmc/articles/PMC4462952/ /pubmed/25904337 http://dx.doi.org/10.1091/mbc.E14-12-1648 Text en © 2015 Larraguibel et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.
spellingShingle Articles
Larraguibel, Jahdiel
Weiss, Alexander R. E.
Pasula, Daniel J.
Dhaliwal, Rasmeet S.
Kondra, Roman
Van Raay, Terence J.
Wnt ligand–dependent activation of the negative feedback regulator Nkd1
title Wnt ligand–dependent activation of the negative feedback regulator Nkd1
title_full Wnt ligand–dependent activation of the negative feedback regulator Nkd1
title_fullStr Wnt ligand–dependent activation of the negative feedback regulator Nkd1
title_full_unstemmed Wnt ligand–dependent activation of the negative feedback regulator Nkd1
title_short Wnt ligand–dependent activation of the negative feedback regulator Nkd1
title_sort wnt ligand–dependent activation of the negative feedback regulator nkd1
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462952/
https://www.ncbi.nlm.nih.gov/pubmed/25904337
http://dx.doi.org/10.1091/mbc.E14-12-1648
work_keys_str_mv AT larraguibeljahdiel wntliganddependentactivationofthenegativefeedbackregulatornkd1
AT weissalexanderre wntliganddependentactivationofthenegativefeedbackregulatornkd1
AT pasuladanielj wntliganddependentactivationofthenegativefeedbackregulatornkd1
AT dhaliwalrasmeets wntliganddependentactivationofthenegativefeedbackregulatornkd1
AT kondraroman wntliganddependentactivationofthenegativefeedbackregulatornkd1
AT vanraayterencej wntliganddependentactivationofthenegativefeedbackregulatornkd1