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Discovery of tissue-specific exons using comprehensive human exon microarrays
BACKGROUND: Higher eukaryotes express a diverse population of messenger RNAs generated by alternative splicing. Large-scale methods for monitoring gene expression must adapt in order to accurately detect the transcript variation generated by this splicing. RESULTS: We have designed a high-density ol...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1896007/ https://www.ncbi.nlm.nih.gov/pubmed/17456239 http://dx.doi.org/10.1186/gb-2007-8-4-r64 |
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author | Clark, Tyson A Schweitzer, Anthony C Chen, Tina X Staples, Michelle K Lu, Gang Wang, Hui Williams, Alan Blume, John E |
author_facet | Clark, Tyson A Schweitzer, Anthony C Chen, Tina X Staples, Michelle K Lu, Gang Wang, Hui Williams, Alan Blume, John E |
author_sort | Clark, Tyson A |
collection | PubMed |
description | BACKGROUND: Higher eukaryotes express a diverse population of messenger RNAs generated by alternative splicing. Large-scale methods for monitoring gene expression must adapt in order to accurately detect the transcript variation generated by this splicing. RESULTS: We have designed a high-density oligonucleotide microarray with probesets for more than one million annotated and predicted exons in the human genome. Using these arrays and a simple algorithm that normalizes exon signal to signal from the gene as a whole, we have identified tissue-specific exons from a panel of 16 different normal adult tissues. RT-PCR validation confirms approximately 86% of the predicted tissue-enriched probesets. Pair-wise comparisons between the tissues suggest that as many as 73% of detected genes are differentially alternatively spliced. We also demonstrate how an inclusive exon microarray can be used to discover novel alternative splicing events. As examples, 17 new tissue-specific exons from 11 genes were validated by RT-PCR and sequencing. CONCLUSION: In conjunction with a conceptually simple algorithm, comprehensive exon microarrays can detect tissue-specific alternative splicing events. Our data suggest significant expression outside of known exons and well annotated genes and a high frequency of alternative splicing events. In addition, we identified and validated a number of novel exons with tissue-specific splicing patterns. The tissue map data will likely serve as a valuable source of information on the regulation of alternative splicing. |
format | Text |
id | pubmed-1896007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18960072007-06-22 Discovery of tissue-specific exons using comprehensive human exon microarrays Clark, Tyson A Schweitzer, Anthony C Chen, Tina X Staples, Michelle K Lu, Gang Wang, Hui Williams, Alan Blume, John E Genome Biol Research BACKGROUND: Higher eukaryotes express a diverse population of messenger RNAs generated by alternative splicing. Large-scale methods for monitoring gene expression must adapt in order to accurately detect the transcript variation generated by this splicing. RESULTS: We have designed a high-density oligonucleotide microarray with probesets for more than one million annotated and predicted exons in the human genome. Using these arrays and a simple algorithm that normalizes exon signal to signal from the gene as a whole, we have identified tissue-specific exons from a panel of 16 different normal adult tissues. RT-PCR validation confirms approximately 86% of the predicted tissue-enriched probesets. Pair-wise comparisons between the tissues suggest that as many as 73% of detected genes are differentially alternatively spliced. We also demonstrate how an inclusive exon microarray can be used to discover novel alternative splicing events. As examples, 17 new tissue-specific exons from 11 genes were validated by RT-PCR and sequencing. CONCLUSION: In conjunction with a conceptually simple algorithm, comprehensive exon microarrays can detect tissue-specific alternative splicing events. Our data suggest significant expression outside of known exons and well annotated genes and a high frequency of alternative splicing events. In addition, we identified and validated a number of novel exons with tissue-specific splicing patterns. The tissue map data will likely serve as a valuable source of information on the regulation of alternative splicing. BioMed Central 2007 2007-04-24 /pmc/articles/PMC1896007/ /pubmed/17456239 http://dx.doi.org/10.1186/gb-2007-8-4-r64 Text en Copyright © 2007 Clark 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 Clark, Tyson A Schweitzer, Anthony C Chen, Tina X Staples, Michelle K Lu, Gang Wang, Hui Williams, Alan Blume, John E Discovery of tissue-specific exons using comprehensive human exon microarrays |
title | Discovery of tissue-specific exons using comprehensive human exon microarrays |
title_full | Discovery of tissue-specific exons using comprehensive human exon microarrays |
title_fullStr | Discovery of tissue-specific exons using comprehensive human exon microarrays |
title_full_unstemmed | Discovery of tissue-specific exons using comprehensive human exon microarrays |
title_short | Discovery of tissue-specific exons using comprehensive human exon microarrays |
title_sort | discovery of tissue-specific exons using comprehensive human exon microarrays |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1896007/ https://www.ncbi.nlm.nih.gov/pubmed/17456239 http://dx.doi.org/10.1186/gb-2007-8-4-r64 |
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