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Proteogenomic Analysis Identifies a Novel Human SHANK3 Isoform

Mutations of the SHANK3 gene have been associated with autism spectrum disorder. Individuals harboring different SHANK3 mutations display considerable heterogeneity in their cognitive impairment, likely due to the high SHANK3 transcriptional diversity. In this study, we report a novel interaction be...

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Autores principales: Benthani, Fahad, Tran, Phuong N., Currey, Nicola, Ng, Irvin, Giry-Laterriere, Marc, Carey, Louise, Kohonen-Corish, Maija R. J., Pangon, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463715/
https://www.ncbi.nlm.nih.gov/pubmed/25997006
http://dx.doi.org/10.3390/ijms160511522
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author Benthani, Fahad
Tran, Phuong N.
Currey, Nicola
Ng, Irvin
Giry-Laterriere, Marc
Carey, Louise
Kohonen-Corish, Maija R. J.
Pangon, Laurent
author_facet Benthani, Fahad
Tran, Phuong N.
Currey, Nicola
Ng, Irvin
Giry-Laterriere, Marc
Carey, Louise
Kohonen-Corish, Maija R. J.
Pangon, Laurent
author_sort Benthani, Fahad
collection PubMed
description Mutations of the SHANK3 gene have been associated with autism spectrum disorder. Individuals harboring different SHANK3 mutations display considerable heterogeneity in their cognitive impairment, likely due to the high SHANK3 transcriptional diversity. In this study, we report a novel interaction between the Mutated in colorectal cancer (MCC) protein and a newly identified SHANK3 protein isoform in human colon cancer cells and mouse brain tissue. Hence, our proteogenomic analysis identifies a new human long isoform of the key synaptic protein SHANK3 that was not predicted by the human reference genome. Taken together, our findings describe a potential new role for MCC in neurons, a new human SHANK3 long isoform and, importantly, highlight the use of proteomic data towards the re-annotation of GC-rich genomic regions.
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spelling pubmed-44637152015-06-16 Proteogenomic Analysis Identifies a Novel Human SHANK3 Isoform Benthani, Fahad Tran, Phuong N. Currey, Nicola Ng, Irvin Giry-Laterriere, Marc Carey, Louise Kohonen-Corish, Maija R. J. Pangon, Laurent Int J Mol Sci Brief Report Mutations of the SHANK3 gene have been associated with autism spectrum disorder. Individuals harboring different SHANK3 mutations display considerable heterogeneity in their cognitive impairment, likely due to the high SHANK3 transcriptional diversity. In this study, we report a novel interaction between the Mutated in colorectal cancer (MCC) protein and a newly identified SHANK3 protein isoform in human colon cancer cells and mouse brain tissue. Hence, our proteogenomic analysis identifies a new human long isoform of the key synaptic protein SHANK3 that was not predicted by the human reference genome. Taken together, our findings describe a potential new role for MCC in neurons, a new human SHANK3 long isoform and, importantly, highlight the use of proteomic data towards the re-annotation of GC-rich genomic regions. MDPI 2015-05-19 /pmc/articles/PMC4463715/ /pubmed/25997006 http://dx.doi.org/10.3390/ijms160511522 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Benthani, Fahad
Tran, Phuong N.
Currey, Nicola
Ng, Irvin
Giry-Laterriere, Marc
Carey, Louise
Kohonen-Corish, Maija R. J.
Pangon, Laurent
Proteogenomic Analysis Identifies a Novel Human SHANK3 Isoform
title Proteogenomic Analysis Identifies a Novel Human SHANK3 Isoform
title_full Proteogenomic Analysis Identifies a Novel Human SHANK3 Isoform
title_fullStr Proteogenomic Analysis Identifies a Novel Human SHANK3 Isoform
title_full_unstemmed Proteogenomic Analysis Identifies a Novel Human SHANK3 Isoform
title_short Proteogenomic Analysis Identifies a Novel Human SHANK3 Isoform
title_sort proteogenomic analysis identifies a novel human shank3 isoform
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463715/
https://www.ncbi.nlm.nih.gov/pubmed/25997006
http://dx.doi.org/10.3390/ijms160511522
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