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Assessing the contribution of alternative splicing to proteome diversity in Arabidopsis thaliana using proteomics data

BACKGROUND: Large-scale analyses of genomics and transcriptomics data have revealed that alternative splicing (AS) substantially increases the complexity of the transcriptome in higher eukaryotes. However, the extent to which this complexity is reflected at the level of the proteome remains unclear....

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Autores principales: Severing, Edouard I, van Dijk, Aalt DJ, van Ham, Roeland CHJ
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118179/
https://www.ncbi.nlm.nih.gov/pubmed/21575182
http://dx.doi.org/10.1186/1471-2229-11-82
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author Severing, Edouard I
van Dijk, Aalt DJ
van Ham, Roeland CHJ
author_facet Severing, Edouard I
van Dijk, Aalt DJ
van Ham, Roeland CHJ
author_sort Severing, Edouard I
collection PubMed
description BACKGROUND: Large-scale analyses of genomics and transcriptomics data have revealed that alternative splicing (AS) substantially increases the complexity of the transcriptome in higher eukaryotes. However, the extent to which this complexity is reflected at the level of the proteome remains unclear. On the basis of a lack of conservation of AS between species, we previously concluded that AS does not frequently serve as a mechanism that enables the production of multiple functional proteins from a single gene. Following this conclusion, we hypothesized that the extent to which AS events contribute to the proteome diversity in Arabidopsis thaliana would be lower than expected on the basis of transcriptomics data. Here, we test this hypothesis by analyzing two large-scale proteomics datasets from Arabidopsis thaliana. RESULTS: A total of only 60 AS events could be confirmed using the proteomics data. However, for about 60% of the loci that, based on transcriptomics data, were predicted to produce multiple protein isoforms through AS, no isoform-specific peptides were found. We therefore performed in silico AS detection experiments to assess how well AS events were represented in the experimental datasets. The results of these in silico experiments indicated that the low number of confirmed AS events was the consequence of a limited sampling depth rather than in vivo under-representation of AS events in these datasets. CONCLUSION: Although the impact of AS on the functional properties of the proteome remains to be uncovered, the results of this study indicate that AS-induced diversity at the transcriptome level is also expressed at the proteome level.
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spelling pubmed-31181792011-06-19 Assessing the contribution of alternative splicing to proteome diversity in Arabidopsis thaliana using proteomics data Severing, Edouard I van Dijk, Aalt DJ van Ham, Roeland CHJ BMC Plant Biol Research Article BACKGROUND: Large-scale analyses of genomics and transcriptomics data have revealed that alternative splicing (AS) substantially increases the complexity of the transcriptome in higher eukaryotes. However, the extent to which this complexity is reflected at the level of the proteome remains unclear. On the basis of a lack of conservation of AS between species, we previously concluded that AS does not frequently serve as a mechanism that enables the production of multiple functional proteins from a single gene. Following this conclusion, we hypothesized that the extent to which AS events contribute to the proteome diversity in Arabidopsis thaliana would be lower than expected on the basis of transcriptomics data. Here, we test this hypothesis by analyzing two large-scale proteomics datasets from Arabidopsis thaliana. RESULTS: A total of only 60 AS events could be confirmed using the proteomics data. However, for about 60% of the loci that, based on transcriptomics data, were predicted to produce multiple protein isoforms through AS, no isoform-specific peptides were found. We therefore performed in silico AS detection experiments to assess how well AS events were represented in the experimental datasets. The results of these in silico experiments indicated that the low number of confirmed AS events was the consequence of a limited sampling depth rather than in vivo under-representation of AS events in these datasets. CONCLUSION: Although the impact of AS on the functional properties of the proteome remains to be uncovered, the results of this study indicate that AS-induced diversity at the transcriptome level is also expressed at the proteome level. BioMed Central 2011-05-16 /pmc/articles/PMC3118179/ /pubmed/21575182 http://dx.doi.org/10.1186/1471-2229-11-82 Text en Copyright ©2011 Severing et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Severing, Edouard I
van Dijk, Aalt DJ
van Ham, Roeland CHJ
Assessing the contribution of alternative splicing to proteome diversity in Arabidopsis thaliana using proteomics data
title Assessing the contribution of alternative splicing to proteome diversity in Arabidopsis thaliana using proteomics data
title_full Assessing the contribution of alternative splicing to proteome diversity in Arabidopsis thaliana using proteomics data
title_fullStr Assessing the contribution of alternative splicing to proteome diversity in Arabidopsis thaliana using proteomics data
title_full_unstemmed Assessing the contribution of alternative splicing to proteome diversity in Arabidopsis thaliana using proteomics data
title_short Assessing the contribution of alternative splicing to proteome diversity in Arabidopsis thaliana using proteomics data
title_sort assessing the contribution of alternative splicing to proteome diversity in arabidopsis thaliana using proteomics data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118179/
https://www.ncbi.nlm.nih.gov/pubmed/21575182
http://dx.doi.org/10.1186/1471-2229-11-82
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