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Splicing factor and exon profiling across human tissues

It has been shown that alternative splicing is especially prevalent in brain and testis when compared to other tissues. To test whether there is a specific propensity of these tissues to generate splicing variants, we used a single source of high-density microarray data to perform both splicing fact...

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Autores principales: de la Grange, Pierre, Gratadou, Lise, Delord, Marc, Dutertre, Martin, Auboeuf, Didier
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875023/
https://www.ncbi.nlm.nih.gov/pubmed/20110256
http://dx.doi.org/10.1093/nar/gkq008
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author de la Grange, Pierre
Gratadou, Lise
Delord, Marc
Dutertre, Martin
Auboeuf, Didier
author_facet de la Grange, Pierre
Gratadou, Lise
Delord, Marc
Dutertre, Martin
Auboeuf, Didier
author_sort de la Grange, Pierre
collection PubMed
description It has been shown that alternative splicing is especially prevalent in brain and testis when compared to other tissues. To test whether there is a specific propensity of these tissues to generate splicing variants, we used a single source of high-density microarray data to perform both splicing factor and exon expression profiling across 11 normal human tissues. Paired comparisons between tissues and an original exon-based statistical group analysis demonstrated after extensive RT-PCR validation that the cerebellum, testis, and spleen had the largest proportion of differentially expressed alternative exons. Variations at the exon level correlated with a larger number of splicing factors being expressed at a high level in the cerebellum, testis and spleen than in other tissues. However, this splicing factor expression profile was similar to a more global gene expression pattern as a larger number of genes had a high expression level in the cerebellum, testis and spleen. In addition to providing a unique resource on expression profiling of alternative splicing variants and splicing factors across human tissues, this study demonstrates that the higher prevalence of alternative splicing in a subset of tissues originates from the larger number of genes, including splicing factors, being expressed than in other tissues.
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spelling pubmed-28750232010-05-24 Splicing factor and exon profiling across human tissues de la Grange, Pierre Gratadou, Lise Delord, Marc Dutertre, Martin Auboeuf, Didier Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics It has been shown that alternative splicing is especially prevalent in brain and testis when compared to other tissues. To test whether there is a specific propensity of these tissues to generate splicing variants, we used a single source of high-density microarray data to perform both splicing factor and exon expression profiling across 11 normal human tissues. Paired comparisons between tissues and an original exon-based statistical group analysis demonstrated after extensive RT-PCR validation that the cerebellum, testis, and spleen had the largest proportion of differentially expressed alternative exons. Variations at the exon level correlated with a larger number of splicing factors being expressed at a high level in the cerebellum, testis and spleen than in other tissues. However, this splicing factor expression profile was similar to a more global gene expression pattern as a larger number of genes had a high expression level in the cerebellum, testis and spleen. In addition to providing a unique resource on expression profiling of alternative splicing variants and splicing factors across human tissues, this study demonstrates that the higher prevalence of alternative splicing in a subset of tissues originates from the larger number of genes, including splicing factors, being expressed than in other tissues. Oxford University Press 2010-05 2010-01-27 /pmc/articles/PMC2875023/ /pubmed/20110256 http://dx.doi.org/10.1093/nar/gkq008 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Gene Regulation, Chromatin and Epigenetics
de la Grange, Pierre
Gratadou, Lise
Delord, Marc
Dutertre, Martin
Auboeuf, Didier
Splicing factor and exon profiling across human tissues
title Splicing factor and exon profiling across human tissues
title_full Splicing factor and exon profiling across human tissues
title_fullStr Splicing factor and exon profiling across human tissues
title_full_unstemmed Splicing factor and exon profiling across human tissues
title_short Splicing factor and exon profiling across human tissues
title_sort splicing factor and exon profiling across human tissues
topic Gene Regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875023/
https://www.ncbi.nlm.nih.gov/pubmed/20110256
http://dx.doi.org/10.1093/nar/gkq008
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