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Alternative Splicing of Transcription Factors' Genes: Beyond the Increase of Proteome Diversity

Functional modification of transcription regulators may lead to developmental changes and phenotypical differences between species. In this work, we study the influence of alternative splicing on transcription factors in human and mouse. Our results show that the impact of alternative splicing on tr...

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Detalles Bibliográficos
Autores principales: Talavera, David, Orozco, Modesto, de la Cruz, Xavier
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709715/
https://www.ncbi.nlm.nih.gov/pubmed/19609452
http://dx.doi.org/10.1155/2009/905894
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author Talavera, David
Orozco, Modesto
de la Cruz, Xavier
author_facet Talavera, David
Orozco, Modesto
de la Cruz, Xavier
author_sort Talavera, David
collection PubMed
description Functional modification of transcription regulators may lead to developmental changes and phenotypical differences between species. In this work, we study the influence of alternative splicing on transcription factors in human and mouse. Our results show that the impact of alternative splicing on transcription factors is similar in both species, meaning that the ways to increase variability should also be similar. However, when looking at the expression patterns of transcription factors, we observe that they tend to diverge regardless of the role of alternative splicing. Finally, we hypothesise that transcription regulation of alternatively spliced transcription factors could play an important role in the phenotypical differences between species, without discarding other phenomena or functional families.
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spelling pubmed-27097152009-07-16 Alternative Splicing of Transcription Factors' Genes: Beyond the Increase of Proteome Diversity Talavera, David Orozco, Modesto de la Cruz, Xavier Comp Funct Genomics Research Article Functional modification of transcription regulators may lead to developmental changes and phenotypical differences between species. In this work, we study the influence of alternative splicing on transcription factors in human and mouse. Our results show that the impact of alternative splicing on transcription factors is similar in both species, meaning that the ways to increase variability should also be similar. However, when looking at the expression patterns of transcription factors, we observe that they tend to diverge regardless of the role of alternative splicing. Finally, we hypothesise that transcription regulation of alternatively spliced transcription factors could play an important role in the phenotypical differences between species, without discarding other phenomena or functional families. Hindawi Publishing Corporation 2009 2009-07-12 /pmc/articles/PMC2709715/ /pubmed/19609452 http://dx.doi.org/10.1155/2009/905894 Text en Copyright © 2009 David Talavera et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Talavera, David
Orozco, Modesto
de la Cruz, Xavier
Alternative Splicing of Transcription Factors' Genes: Beyond the Increase of Proteome Diversity
title Alternative Splicing of Transcription Factors' Genes: Beyond the Increase of Proteome Diversity
title_full Alternative Splicing of Transcription Factors' Genes: Beyond the Increase of Proteome Diversity
title_fullStr Alternative Splicing of Transcription Factors' Genes: Beyond the Increase of Proteome Diversity
title_full_unstemmed Alternative Splicing of Transcription Factors' Genes: Beyond the Increase of Proteome Diversity
title_short Alternative Splicing of Transcription Factors' Genes: Beyond the Increase of Proteome Diversity
title_sort alternative splicing of transcription factors' genes: beyond the increase of proteome diversity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709715/
https://www.ncbi.nlm.nih.gov/pubmed/19609452
http://dx.doi.org/10.1155/2009/905894
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