Comparison of p53 and the PDZ domain containing protein MAGI-3 regulation by the E6 protein from high-risk human papillomaviruses

<p>Abstract</p> <p>Central to cellular transformation caused by human papillomaviruses (HPVs) is the ability of E6 proteins to target cellular p53 and proteins containing PDZ domains, including MAGI-3, for degradation. The aim of this study was to compare E6-mediated degradation of...

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Main Authors: Coutlee Francois, Banks Lawrence, Thomas Miranda, Ainsworth Julia, Matlashewski Greg
Format: Article
Language:English
Published: BMC 2008-06-01
Series:Virology Journal
Online Access:http://www.virologyj.com/content/5/1/67
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spelling doaj-77e5ffd506fd408680b50065f16e26152020-11-25T00:21:45ZengBMCVirology Journal1743-422X2008-06-01516710.1186/1743-422X-5-67Comparison of p53 and the PDZ domain containing protein MAGI-3 regulation by the E6 protein from high-risk human papillomavirusesCoutlee FrancoisBanks LawrenceThomas MirandaAinsworth JuliaMatlashewski Greg<p>Abstract</p> <p>Central to cellular transformation caused by human papillomaviruses (HPVs) is the ability of E6 proteins to target cellular p53 and proteins containing PDZ domains, including MAGI-3, for degradation. The aim of this study was to compare E6-mediated degradation of p53 and MAGI-3 under parallel experimental conditions and further with respect to the involvement of proteasomes and ubiquitination. We also compared the degradation of p53 and MAGI-3 by E6 from several HPV types including different variants from HPV-33. All of the E6 genes from different HPV types displayed similar abilities to mediate the degradation of both p53 and MAGI-3 although there may be subtle differences observed with the different 33E6 variants. There were however differences in E6 mediated degradation of p53 and MAGI-3. Proteasome inhibition assays partially protected p53 from E6 mediated degradation, but did not protect MAGI-3. In addition, under conditions where p53 was ubiquitinated by E6 and MDM2 <it>in vivo</it>, ubiquitination of MAGI-3 was not detected. These results imply that although both p53 and MAGI-3 represent effective targets for oncogenic E6, the mechanisms by which E6 mediates p53 and MAGI-3 degradation are distinct with respect to the involvement of ubiquitination prior to proteasomal degradation.</p> http://www.virologyj.com/content/5/1/67
collection DOAJ
language English
format Article
sources DOAJ
author Coutlee Francois
Banks Lawrence
Thomas Miranda
Ainsworth Julia
Matlashewski Greg
spellingShingle Coutlee Francois
Banks Lawrence
Thomas Miranda
Ainsworth Julia
Matlashewski Greg
Comparison of p53 and the PDZ domain containing protein MAGI-3 regulation by the E6 protein from high-risk human papillomaviruses
Virology Journal
author_facet Coutlee Francois
Banks Lawrence
Thomas Miranda
Ainsworth Julia
Matlashewski Greg
author_sort Coutlee Francois
title Comparison of p53 and the PDZ domain containing protein MAGI-3 regulation by the E6 protein from high-risk human papillomaviruses
title_short Comparison of p53 and the PDZ domain containing protein MAGI-3 regulation by the E6 protein from high-risk human papillomaviruses
title_full Comparison of p53 and the PDZ domain containing protein MAGI-3 regulation by the E6 protein from high-risk human papillomaviruses
title_fullStr Comparison of p53 and the PDZ domain containing protein MAGI-3 regulation by the E6 protein from high-risk human papillomaviruses
title_full_unstemmed Comparison of p53 and the PDZ domain containing protein MAGI-3 regulation by the E6 protein from high-risk human papillomaviruses
title_sort comparison of p53 and the pdz domain containing protein magi-3 regulation by the e6 protein from high-risk human papillomaviruses
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2008-06-01
description <p>Abstract</p> <p>Central to cellular transformation caused by human papillomaviruses (HPVs) is the ability of E6 proteins to target cellular p53 and proteins containing PDZ domains, including MAGI-3, for degradation. The aim of this study was to compare E6-mediated degradation of p53 and MAGI-3 under parallel experimental conditions and further with respect to the involvement of proteasomes and ubiquitination. We also compared the degradation of p53 and MAGI-3 by E6 from several HPV types including different variants from HPV-33. All of the E6 genes from different HPV types displayed similar abilities to mediate the degradation of both p53 and MAGI-3 although there may be subtle differences observed with the different 33E6 variants. There were however differences in E6 mediated degradation of p53 and MAGI-3. Proteasome inhibition assays partially protected p53 from E6 mediated degradation, but did not protect MAGI-3. In addition, under conditions where p53 was ubiquitinated by E6 and MDM2 <it>in vivo</it>, ubiquitination of MAGI-3 was not detected. These results imply that although both p53 and MAGI-3 represent effective targets for oncogenic E6, the mechanisms by which E6 mediates p53 and MAGI-3 degradation are distinct with respect to the involvement of ubiquitination prior to proteasomal degradation.</p>
url http://www.virologyj.com/content/5/1/67
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