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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2012
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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. |
format | Online Article Text |
id | pubmed-3408978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
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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