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The RNA Splicing Response to DNA Damage

The number of factors known to participate in the DNA damage response (DDR) has expanded considerably in recent years to include splicing and alternative splicing factors. While the binding of splicing proteins and ribonucleoprotein complexes to nascent transcripts prevents genomic instability by de...

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Detalles Bibliográficos
Autores principales: Shkreta, Lulzim, Chabot, Benoit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693264/
https://www.ncbi.nlm.nih.gov/pubmed/26529031
http://dx.doi.org/10.3390/biom5042935
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author Shkreta, Lulzim
Chabot, Benoit
author_facet Shkreta, Lulzim
Chabot, Benoit
author_sort Shkreta, Lulzim
collection PubMed
description The number of factors known to participate in the DNA damage response (DDR) has expanded considerably in recent years to include splicing and alternative splicing factors. While the binding of splicing proteins and ribonucleoprotein complexes to nascent transcripts prevents genomic instability by deterring the formation of RNA/DNA duplexes, splicing factors are also recruited to, or removed from, sites of DNA damage. The first steps of the DDR promote the post-translational modification of splicing factors to affect their localization and activity, while more downstream DDR events alter their expression. Although descriptions of molecular mechanisms remain limited, an emerging trend is that DNA damage disrupts the coupling of constitutive and alternative splicing with the transcription of genes involved in DNA repair, cell-cycle control and apoptosis. A better understanding of how changes in splice site selection are integrated into the DDR may provide new avenues to combat cancer and delay aging.
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spelling pubmed-46932642016-01-07 The RNA Splicing Response to DNA Damage Shkreta, Lulzim Chabot, Benoit Biomolecules Review The number of factors known to participate in the DNA damage response (DDR) has expanded considerably in recent years to include splicing and alternative splicing factors. While the binding of splicing proteins and ribonucleoprotein complexes to nascent transcripts prevents genomic instability by deterring the formation of RNA/DNA duplexes, splicing factors are also recruited to, or removed from, sites of DNA damage. The first steps of the DDR promote the post-translational modification of splicing factors to affect their localization and activity, while more downstream DDR events alter their expression. Although descriptions of molecular mechanisms remain limited, an emerging trend is that DNA damage disrupts the coupling of constitutive and alternative splicing with the transcription of genes involved in DNA repair, cell-cycle control and apoptosis. A better understanding of how changes in splice site selection are integrated into the DDR may provide new avenues to combat cancer and delay aging. MDPI 2015-10-29 /pmc/articles/PMC4693264/ /pubmed/26529031 http://dx.doi.org/10.3390/biom5042935 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Shkreta, Lulzim
Chabot, Benoit
The RNA Splicing Response to DNA Damage
title The RNA Splicing Response to DNA Damage
title_full The RNA Splicing Response to DNA Damage
title_fullStr The RNA Splicing Response to DNA Damage
title_full_unstemmed The RNA Splicing Response to DNA Damage
title_short The RNA Splicing Response to DNA Damage
title_sort rna splicing response to dna damage
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693264/
https://www.ncbi.nlm.nih.gov/pubmed/26529031
http://dx.doi.org/10.3390/biom5042935
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