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Neuroepithelial Transforming Gene 1 (Net1) Binds to Caspase Activation and Recruitment Domain (CARD)- and Membrane-associated Guanylate Kinase-like Domain-containing (CARMA) Proteins and Regulates Nuclear Factor κB Activation

The molecular complexes containing CARMA proteins have been recently identified as a key components in the signal transduction pathways that regulate activation of nuclear factor κB (NF-κB) transcription factor. Here, we used immunoprecipitation coupled with mass spectrometry to identify cellular bi...

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Autores principales: Vessichelli, Mariangela, Ferravante, Angela, Zotti, Tiziana, Reale, Carla, Scudiero, Ivan, Picariello, Gianluca, Vito, Pasquale, Stilo, Romania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340137/
https://www.ncbi.nlm.nih.gov/pubmed/22343628
http://dx.doi.org/10.1074/jbc.M111.304436
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author Vessichelli, Mariangela
Ferravante, Angela
Zotti, Tiziana
Reale, Carla
Scudiero, Ivan
Picariello, Gianluca
Vito, Pasquale
Stilo, Romania
author_facet Vessichelli, Mariangela
Ferravante, Angela
Zotti, Tiziana
Reale, Carla
Scudiero, Ivan
Picariello, Gianluca
Vito, Pasquale
Stilo, Romania
author_sort Vessichelli, Mariangela
collection PubMed
description The molecular complexes containing CARMA proteins have been recently identified as a key components in the signal transduction pathways that regulate activation of nuclear factor κB (NF-κB) transcription factor. Here, we used immunoprecipitation coupled with mass spectrometry to identify cellular binding partners of CARMA proteins. Our data indicate that the Rho guanine nucleotide exchange factor Net1 binds to CARMA1 and CARMA3 in resting and activated cells. Net1 expression induces NF-κB activation and cooperates with BCL10 and CARMA proteins in inducing NF-κB activity. Conversely, shRNA-mediated abrogation of Net1 results in impaired NF-κB activation following stimuli that require correct CARMA-BCL10-MALT1 complex formation and functioning. Microarray expression data are consistent with a positive role for Net1 on NF-κB activation. Thus, this study identifies Net1 as a CARMA-interacting molecule and brings important information on the molecular mechanisms that control NF-κB transcriptional activity.
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spelling pubmed-33401372012-05-02 Neuroepithelial Transforming Gene 1 (Net1) Binds to Caspase Activation and Recruitment Domain (CARD)- and Membrane-associated Guanylate Kinase-like Domain-containing (CARMA) Proteins and Regulates Nuclear Factor κB Activation Vessichelli, Mariangela Ferravante, Angela Zotti, Tiziana Reale, Carla Scudiero, Ivan Picariello, Gianluca Vito, Pasquale Stilo, Romania J Biol Chem Signal Transduction The molecular complexes containing CARMA proteins have been recently identified as a key components in the signal transduction pathways that regulate activation of nuclear factor κB (NF-κB) transcription factor. Here, we used immunoprecipitation coupled with mass spectrometry to identify cellular binding partners of CARMA proteins. Our data indicate that the Rho guanine nucleotide exchange factor Net1 binds to CARMA1 and CARMA3 in resting and activated cells. Net1 expression induces NF-κB activation and cooperates with BCL10 and CARMA proteins in inducing NF-κB activity. Conversely, shRNA-mediated abrogation of Net1 results in impaired NF-κB activation following stimuli that require correct CARMA-BCL10-MALT1 complex formation and functioning. Microarray expression data are consistent with a positive role for Net1 on NF-κB activation. Thus, this study identifies Net1 as a CARMA-interacting molecule and brings important information on the molecular mechanisms that control NF-κB transcriptional activity. American Society for Biochemistry and Molecular Biology 2012-04-20 2012-02-16 /pmc/articles/PMC3340137/ /pubmed/22343628 http://dx.doi.org/10.1074/jbc.M111.304436 Text en © 2012 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) applies to Author Choice Articles
spellingShingle Signal Transduction
Vessichelli, Mariangela
Ferravante, Angela
Zotti, Tiziana
Reale, Carla
Scudiero, Ivan
Picariello, Gianluca
Vito, Pasquale
Stilo, Romania
Neuroepithelial Transforming Gene 1 (Net1) Binds to Caspase Activation and Recruitment Domain (CARD)- and Membrane-associated Guanylate Kinase-like Domain-containing (CARMA) Proteins and Regulates Nuclear Factor κB Activation
title Neuroepithelial Transforming Gene 1 (Net1) Binds to Caspase Activation and Recruitment Domain (CARD)- and Membrane-associated Guanylate Kinase-like Domain-containing (CARMA) Proteins and Regulates Nuclear Factor κB Activation
title_full Neuroepithelial Transforming Gene 1 (Net1) Binds to Caspase Activation and Recruitment Domain (CARD)- and Membrane-associated Guanylate Kinase-like Domain-containing (CARMA) Proteins and Regulates Nuclear Factor κB Activation
title_fullStr Neuroepithelial Transforming Gene 1 (Net1) Binds to Caspase Activation and Recruitment Domain (CARD)- and Membrane-associated Guanylate Kinase-like Domain-containing (CARMA) Proteins and Regulates Nuclear Factor κB Activation
title_full_unstemmed Neuroepithelial Transforming Gene 1 (Net1) Binds to Caspase Activation and Recruitment Domain (CARD)- and Membrane-associated Guanylate Kinase-like Domain-containing (CARMA) Proteins and Regulates Nuclear Factor κB Activation
title_short Neuroepithelial Transforming Gene 1 (Net1) Binds to Caspase Activation and Recruitment Domain (CARD)- and Membrane-associated Guanylate Kinase-like Domain-containing (CARMA) Proteins and Regulates Nuclear Factor κB Activation
title_sort neuroepithelial transforming gene 1 (net1) binds to caspase activation and recruitment domain (card)- and membrane-associated guanylate kinase-like domain-containing (carma) proteins and regulates nuclear factor κb activation
topic Signal Transduction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340137/
https://www.ncbi.nlm.nih.gov/pubmed/22343628
http://dx.doi.org/10.1074/jbc.M111.304436
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