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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...

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Autores principales: Clark, Tyson A, Schweitzer, Anthony C, Chen, Tina X, Staples, Michelle K, Lu, Gang, Wang, Hui, Williams, Alan, Blume, John E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
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.
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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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