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Alternative splicing: the pledge, the turn, and the prestige: The key role of alternative splicing in human biological systems

Alternative pre-mRNA splicing is a tightly controlled process conducted by the spliceosome, with the assistance of several regulators, resulting in the expression of different transcript isoforms from the same gene and increasing both transcriptome and proteome complexity. The differences between al...

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Autores principales: Gallego-Paez, L. M., Bordone, M. C., Leote, A. C., Saraiva-Agostinho, N., Ascensão-Ferreira, M., Barbosa-Morais, N. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602094/
https://www.ncbi.nlm.nih.gov/pubmed/28374191
http://dx.doi.org/10.1007/s00439-017-1790-y
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author Gallego-Paez, L. M.
Bordone, M. C.
Leote, A. C.
Saraiva-Agostinho, N.
Ascensão-Ferreira, M.
Barbosa-Morais, N. L.
author_facet Gallego-Paez, L. M.
Bordone, M. C.
Leote, A. C.
Saraiva-Agostinho, N.
Ascensão-Ferreira, M.
Barbosa-Morais, N. L.
author_sort Gallego-Paez, L. M.
collection PubMed
description Alternative pre-mRNA splicing is a tightly controlled process conducted by the spliceosome, with the assistance of several regulators, resulting in the expression of different transcript isoforms from the same gene and increasing both transcriptome and proteome complexity. The differences between alternative isoforms may be subtle but enough to change the function or localization of the translated proteins. A fine control of the isoform balance is, therefore, needed throughout developmental stages and adult tissues or physiological conditions and it does not come as a surprise that several diseases are caused by its deregulation. In this review, we aim to bring the splicing machinery on stage and raise the curtain on its mechanisms and regulation throughout several systems and tissues of the human body, from neurodevelopment to the interactions with the human microbiome. We discuss, on one hand, the essential role of alternative splicing in assuring tissue function, diversity, and swiftness of response in these systems or tissues, and on the other hand, what goes wrong when its regulatory mechanisms fail. We also focus on the possibilities that splicing modulation therapies open for the future of personalized medicine, along with the leading techniques in this field. The final act of the spliceosome, however, is yet to be fully revealed, as more knowledge is needed regarding the complex regulatory network that coordinates alternative splicing and how its dysfunction leads to disease.
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spelling pubmed-56020942017-10-03 Alternative splicing: the pledge, the turn, and the prestige: The key role of alternative splicing in human biological systems Gallego-Paez, L. M. Bordone, M. C. Leote, A. C. Saraiva-Agostinho, N. Ascensão-Ferreira, M. Barbosa-Morais, N. L. Hum Genet Review Alternative pre-mRNA splicing is a tightly controlled process conducted by the spliceosome, with the assistance of several regulators, resulting in the expression of different transcript isoforms from the same gene and increasing both transcriptome and proteome complexity. The differences between alternative isoforms may be subtle but enough to change the function or localization of the translated proteins. A fine control of the isoform balance is, therefore, needed throughout developmental stages and adult tissues or physiological conditions and it does not come as a surprise that several diseases are caused by its deregulation. In this review, we aim to bring the splicing machinery on stage and raise the curtain on its mechanisms and regulation throughout several systems and tissues of the human body, from neurodevelopment to the interactions with the human microbiome. We discuss, on one hand, the essential role of alternative splicing in assuring tissue function, diversity, and swiftness of response in these systems or tissues, and on the other hand, what goes wrong when its regulatory mechanisms fail. We also focus on the possibilities that splicing modulation therapies open for the future of personalized medicine, along with the leading techniques in this field. The final act of the spliceosome, however, is yet to be fully revealed, as more knowledge is needed regarding the complex regulatory network that coordinates alternative splicing and how its dysfunction leads to disease. Springer Berlin Heidelberg 2017-04-03 2017 /pmc/articles/PMC5602094/ /pubmed/28374191 http://dx.doi.org/10.1007/s00439-017-1790-y Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Gallego-Paez, L. M.
Bordone, M. C.
Leote, A. C.
Saraiva-Agostinho, N.
Ascensão-Ferreira, M.
Barbosa-Morais, N. L.
Alternative splicing: the pledge, the turn, and the prestige: The key role of alternative splicing in human biological systems
title Alternative splicing: the pledge, the turn, and the prestige: The key role of alternative splicing in human biological systems
title_full Alternative splicing: the pledge, the turn, and the prestige: The key role of alternative splicing in human biological systems
title_fullStr Alternative splicing: the pledge, the turn, and the prestige: The key role of alternative splicing in human biological systems
title_full_unstemmed Alternative splicing: the pledge, the turn, and the prestige: The key role of alternative splicing in human biological systems
title_short Alternative splicing: the pledge, the turn, and the prestige: The key role of alternative splicing in human biological systems
title_sort alternative splicing: the pledge, the turn, and the prestige: the key role of alternative splicing in human biological systems
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602094/
https://www.ncbi.nlm.nih.gov/pubmed/28374191
http://dx.doi.org/10.1007/s00439-017-1790-y
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