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IAPs as E3 ligases of Rac1: Shaping the move

Inhibitors of Apoptosis Proteins (IAPs) are well-studied E3 ubiquitin ligases predominantly known for regulation of apoptosis. We uncovered that IAPs can function as a direct E3 ubiquitin ligase of RhoGTPase Rac1. cIAP1 and XIAP directly conjugate polyubiquitin chains to Lysine 147 of activated Rac1...

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Autores principales: Oberoi-Khanuja, Tripat Kaur, Rajalingam, Krishnaraj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408978/
https://www.ncbi.nlm.nih.gov/pubmed/22790203
http://dx.doi.org/10.4161/sgtp.19988
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author Oberoi-Khanuja, Tripat Kaur
Rajalingam, Krishnaraj
author_facet Oberoi-Khanuja, Tripat Kaur
Rajalingam, Krishnaraj
author_sort Oberoi-Khanuja, Tripat Kaur
collection PubMed
description Inhibitors of Apoptosis Proteins (IAPs) are well-studied E3 ubiquitin ligases predominantly known for regulation of apoptosis. We uncovered that IAPs can function as a direct E3 ubiquitin ligase of RhoGTPase Rac1. cIAP1 and XIAP directly conjugate polyubiquitin chains to Lysine 147 of activated Rac1 and target it for proteasomal degradation. Consistently, loss of these IAPs by various strategies led to stabilization of Rac1 and mesenchymal mode of migration in tumor cells. IAPs also regulate Rac1 degradation upon RhoGDI1 depletion and CNF1 toxin treatment. Our observations revealed an evolutionarily conserved role of IAPs in regulating Rac1 stability shedding light on to the mechanisms behind ubiquitination–dependent inactivation of Rac1 signaling.
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spelling pubmed-34089782012-08-07 IAPs as E3 ligases of Rac1: Shaping the move Oberoi-Khanuja, Tripat Kaur Rajalingam, Krishnaraj Small GTPases Commentary Inhibitors of Apoptosis Proteins (IAPs) are well-studied E3 ubiquitin ligases predominantly known for regulation of apoptosis. We uncovered that IAPs can function as a direct E3 ubiquitin ligase of RhoGTPase Rac1. cIAP1 and XIAP directly conjugate polyubiquitin chains to Lysine 147 of activated Rac1 and target it for proteasomal degradation. Consistently, loss of these IAPs by various strategies led to stabilization of Rac1 and mesenchymal mode of migration in tumor cells. IAPs also regulate Rac1 degradation upon RhoGDI1 depletion and CNF1 toxin treatment. Our observations revealed an evolutionarily conserved role of IAPs in regulating Rac1 stability shedding light on to the mechanisms behind ubiquitination–dependent inactivation of Rac1 signaling. Landes Bioscience 2012-04-01 /pmc/articles/PMC3408978/ /pubmed/22790203 http://dx.doi.org/10.4161/sgtp.19988 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 Commentary
Oberoi-Khanuja, Tripat Kaur
Rajalingam, Krishnaraj
IAPs as E3 ligases of Rac1: Shaping the move
title IAPs as E3 ligases of Rac1: Shaping the move
title_full IAPs as E3 ligases of Rac1: Shaping the move
title_fullStr IAPs as E3 ligases of Rac1: Shaping the move
title_full_unstemmed IAPs as E3 ligases of Rac1: Shaping the move
title_short IAPs as E3 ligases of Rac1: Shaping the move
title_sort iaps as e3 ligases of rac1: shaping the move
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3408978/
https://www.ncbi.nlm.nih.gov/pubmed/22790203
http://dx.doi.org/10.4161/sgtp.19988
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