Determining the impact of alternative splicing events on transcriptome dynamics

<p>Abstract</p> <p>Background</p> <p>The complete sequencing of the human genome and its subsequent analysis revealed a predominant role for alternative splicing in the generation of proteome diversity. Splice switching oligonucleotides (SSOs) are a powerful and specifi...

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Main Authors: Bell Brendan, Benecke Arndt, Pellay François-Xavier, Wilhelm Emmanuelle
Format: Article
Language:English
Published: BMC 2008-10-01
Series:BMC Research Notes
Online Access:http://www.biomedcentral.com/1756-0500/1/94
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spelling doaj-bd1826cfa8a94c0aa8dece38a3b4a4db2020-11-25T01:54:26ZengBMCBMC Research Notes1756-05002008-10-01119410.1186/1756-0500-1-94Determining the impact of alternative splicing events on transcriptome dynamicsBell BrendanBenecke ArndtPellay François-XavierWilhelm Emmanuelle<p>Abstract</p> <p>Background</p> <p>The complete sequencing of the human genome and its subsequent analysis revealed a predominant role for alternative splicing in the generation of proteome diversity. Splice switching oligonucleotides (SSOs) are a powerful and specific tool to experimentally control alternative splicing of endogenous messenger RNAs in living cells. SSOs also have therapeutic potential to treat diseases that are caused by aberrant splicing. The assignment of biological roles to alternative splicing events of currently unknown function promises to provide a largely untapped source of potential new therapeutic targets. Here we have developed a protocol that combines high sensitivity microarrays with the transfection of SSOs to monitor global changes in gene expression downstream of alternate, endogenous splice events.</p> <p>Results</p> <p>When applied to a well-characterized splicing event in the Bcl-x gene, the application of high sensitivity microarrays revealed a link between the induction of the Bcl-xS isoform and the repression of genes involved in protein synthesis.</p> <p>Conclusion</p> <p>The strategy introduced herein provides a useful approach to define the biological impact of any given alternative splicing event on global gene expression patterns. Furthermore, our data provide the first link between Bcl-xS expression and the repression of ribosomal protein gene expression.</p> http://www.biomedcentral.com/1756-0500/1/94
collection DOAJ
language English
format Article
sources DOAJ
author Bell Brendan
Benecke Arndt
Pellay François-Xavier
Wilhelm Emmanuelle
spellingShingle Bell Brendan
Benecke Arndt
Pellay François-Xavier
Wilhelm Emmanuelle
Determining the impact of alternative splicing events on transcriptome dynamics
BMC Research Notes
author_facet Bell Brendan
Benecke Arndt
Pellay François-Xavier
Wilhelm Emmanuelle
author_sort Bell Brendan
title Determining the impact of alternative splicing events on transcriptome dynamics
title_short Determining the impact of alternative splicing events on transcriptome dynamics
title_full Determining the impact of alternative splicing events on transcriptome dynamics
title_fullStr Determining the impact of alternative splicing events on transcriptome dynamics
title_full_unstemmed Determining the impact of alternative splicing events on transcriptome dynamics
title_sort determining the impact of alternative splicing events on transcriptome dynamics
publisher BMC
series BMC Research Notes
issn 1756-0500
publishDate 2008-10-01
description <p>Abstract</p> <p>Background</p> <p>The complete sequencing of the human genome and its subsequent analysis revealed a predominant role for alternative splicing in the generation of proteome diversity. Splice switching oligonucleotides (SSOs) are a powerful and specific tool to experimentally control alternative splicing of endogenous messenger RNAs in living cells. SSOs also have therapeutic potential to treat diseases that are caused by aberrant splicing. The assignment of biological roles to alternative splicing events of currently unknown function promises to provide a largely untapped source of potential new therapeutic targets. Here we have developed a protocol that combines high sensitivity microarrays with the transfection of SSOs to monitor global changes in gene expression downstream of alternate, endogenous splice events.</p> <p>Results</p> <p>When applied to a well-characterized splicing event in the Bcl-x gene, the application of high sensitivity microarrays revealed a link between the induction of the Bcl-xS isoform and the repression of genes involved in protein synthesis.</p> <p>Conclusion</p> <p>The strategy introduced herein provides a useful approach to define the biological impact of any given alternative splicing event on global gene expression patterns. Furthermore, our data provide the first link between Bcl-xS expression and the repression of ribosomal protein gene expression.</p>
url http://www.biomedcentral.com/1756-0500/1/94
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