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Challenging the spliceosome machine

BACKGROUND: Using cDNA copies of transcripts and corresponding genomic sequences from the Berkeley Drosophila Genome Project, a set of 24,753 donor and acceptor splice sites were computed with a scanning algorithm that tested for single nucleotide insertion, deletion and substitution polymorphisms....

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Detalles Bibliográficos
Autores principales: Weir, Michael, Eaton, Matthew, Rice, Michael
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1431713/
https://www.ncbi.nlm.nih.gov/pubmed/16507135
http://dx.doi.org/10.1186/gb-2006-7-1-r3
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author Weir, Michael
Eaton, Matthew
Rice, Michael
author_facet Weir, Michael
Eaton, Matthew
Rice, Michael
author_sort Weir, Michael
collection PubMed
description BACKGROUND: Using cDNA copies of transcripts and corresponding genomic sequences from the Berkeley Drosophila Genome Project, a set of 24,753 donor and acceptor splice sites were computed with a scanning algorithm that tested for single nucleotide insertion, deletion and substitution polymorphisms. Using this dataset, we developed a progressive partitioning approach to examining the effects of challenging the spliceosome system. RESULTS: Our analysis shows that information content increases near splice sites flanking progressively longer introns and exons, suggesting that longer splice elements require stronger binding of spliceosome components. Information also increases at splice sites near very short introns and exons, suggesting that short splice elements have crowding problems. We observe that the information found at individual splice sites depends upon a balance of splice element lengths in the vicinity, including both flanking and non-adjacent introns and exons. CONCLUSION: These results suggest an interdependence of multiple splicing events along the pre-mRNA, which may have implications for how the macromolecular spliceosome machine processes sets of neighboring splice sites.
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spelling pubmed-14317132006-04-07 Challenging the spliceosome machine Weir, Michael Eaton, Matthew Rice, Michael Genome Biol Research BACKGROUND: Using cDNA copies of transcripts and corresponding genomic sequences from the Berkeley Drosophila Genome Project, a set of 24,753 donor and acceptor splice sites were computed with a scanning algorithm that tested for single nucleotide insertion, deletion and substitution polymorphisms. Using this dataset, we developed a progressive partitioning approach to examining the effects of challenging the spliceosome system. RESULTS: Our analysis shows that information content increases near splice sites flanking progressively longer introns and exons, suggesting that longer splice elements require stronger binding of spliceosome components. Information also increases at splice sites near very short introns and exons, suggesting that short splice elements have crowding problems. We observe that the information found at individual splice sites depends upon a balance of splice element lengths in the vicinity, including both flanking and non-adjacent introns and exons. CONCLUSION: These results suggest an interdependence of multiple splicing events along the pre-mRNA, which may have implications for how the macromolecular spliceosome machine processes sets of neighboring splice sites. BioMed Central 2006 2006-01-17 /pmc/articles/PMC1431713/ /pubmed/16507135 http://dx.doi.org/10.1186/gb-2006-7-1-r3 Text en Copyright © 2006 Weir et al.; licensee BioMed Central Ltd.
spellingShingle Research
Weir, Michael
Eaton, Matthew
Rice, Michael
Challenging the spliceosome machine
title Challenging the spliceosome machine
title_full Challenging the spliceosome machine
title_fullStr Challenging the spliceosome machine
title_full_unstemmed Challenging the spliceosome machine
title_short Challenging the spliceosome machine
title_sort challenging the spliceosome machine
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1431713/
https://www.ncbi.nlm.nih.gov/pubmed/16507135
http://dx.doi.org/10.1186/gb-2006-7-1-r3
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