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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...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2010
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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. |
format | Text |
id | pubmed-2875023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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