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Regulation of ligand-independent Notch signal through intracellular trafficking

Notch signaling is an evolutionarily conserved mechanism that defines a key cell fate control mechanism in metazoans. Notch signaling relies on the surface interaction between the Notch receptor and membrane bound ligands in an apposing cell. In our recent study,(22) we uncover a non-canonical recep...

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Detalles Bibliográficos
Autores principales: Hori, Kazuya, Sen, Anindya, Kirchhausen, Tom, Artavanis-Tsakonas, Spyros
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460843/
https://www.ncbi.nlm.nih.gov/pubmed/23060962
http://dx.doi.org/10.4161/cib.19995
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author Hori, Kazuya
Sen, Anindya
Kirchhausen, Tom
Artavanis-Tsakonas, Spyros
author_facet Hori, Kazuya
Sen, Anindya
Kirchhausen, Tom
Artavanis-Tsakonas, Spyros
author_sort Hori, Kazuya
collection PubMed
description Notch signaling is an evolutionarily conserved mechanism that defines a key cell fate control mechanism in metazoans. Notch signaling relies on the surface interaction between the Notch receptor and membrane bound ligands in an apposing cell. In our recent study,(22) we uncover a non-canonical receptor activation path that relies on a ligand-independent, intracellular activation of the receptor as it travels through the endosomal compartments. We found that Notch receptor, targeted for degradation lysosomal degradation through multivesicular bodies (MVBs) is “diverted” toward activation upon mono-ubiquitination through a synergy between the ubiquitin ligase Deltex, the non-visual β-arrestin Kurtz and the ESCRT-III component Shrub. This activation path is not universal but appears to depend on the cellular context.
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spelling pubmed-34608432012-10-11 Regulation of ligand-independent Notch signal through intracellular trafficking Hori, Kazuya Sen, Anindya Kirchhausen, Tom Artavanis-Tsakonas, Spyros Commun Integr Biol Article Addendum Notch signaling is an evolutionarily conserved mechanism that defines a key cell fate control mechanism in metazoans. Notch signaling relies on the surface interaction between the Notch receptor and membrane bound ligands in an apposing cell. In our recent study,(22) we uncover a non-canonical receptor activation path that relies on a ligand-independent, intracellular activation of the receptor as it travels through the endosomal compartments. We found that Notch receptor, targeted for degradation lysosomal degradation through multivesicular bodies (MVBs) is “diverted” toward activation upon mono-ubiquitination through a synergy between the ubiquitin ligase Deltex, the non-visual β-arrestin Kurtz and the ESCRT-III component Shrub. This activation path is not universal but appears to depend on the cellular context. Landes Bioscience 2012-07-01 /pmc/articles/PMC3460843/ /pubmed/23060962 http://dx.doi.org/10.4161/cib.19995 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Article Addendum
Hori, Kazuya
Sen, Anindya
Kirchhausen, Tom
Artavanis-Tsakonas, Spyros
Regulation of ligand-independent Notch signal through intracellular trafficking
title Regulation of ligand-independent Notch signal through intracellular trafficking
title_full Regulation of ligand-independent Notch signal through intracellular trafficking
title_fullStr Regulation of ligand-independent Notch signal through intracellular trafficking
title_full_unstemmed Regulation of ligand-independent Notch signal through intracellular trafficking
title_short Regulation of ligand-independent Notch signal through intracellular trafficking
title_sort regulation of ligand-independent notch signal through intracellular trafficking
topic Article Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460843/
https://www.ncbi.nlm.nih.gov/pubmed/23060962
http://dx.doi.org/10.4161/cib.19995
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