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RNA Splicing: A New Player in the DNA Damage Response

It is widely accepted that tumorigenesis is a multistep process characterized by the sequential accumulation of genetic alterations. However, the molecular basis of genomic instability in cancer is still partially understood. The observation that hereditary cancers are often characterized by mutatio...

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Detalles Bibliográficos
Autores principales: Lenzken, Silvia C., Loffreda, Alessia, Barabino, Silvia M. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789447/
https://www.ncbi.nlm.nih.gov/pubmed/24159334
http://dx.doi.org/10.1155/2013/153634
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author Lenzken, Silvia C.
Loffreda, Alessia
Barabino, Silvia M. L.
author_facet Lenzken, Silvia C.
Loffreda, Alessia
Barabino, Silvia M. L.
author_sort Lenzken, Silvia C.
collection PubMed
description It is widely accepted that tumorigenesis is a multistep process characterized by the sequential accumulation of genetic alterations. However, the molecular basis of genomic instability in cancer is still partially understood. The observation that hereditary cancers are often characterized by mutations in DNA repair and checkpoint genes suggests that accumulation of DNA damage is a major contributor to the oncogenic transformation. It is therefore of great interest to identify all the cellular pathways that contribute to the response to DNA damage. Recently, RNA processing has emerged as a novel pathway that may contribute to the maintenance of genome stability. In this review, we illustrate several different mechanisms through which pre-mRNA splicing and genomic stability can influence each other. We specifically focus on the role of splicing factors in the DNA damage response and describe how, in turn, activation of the DDR can influence the activity of splicing factors.
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spelling pubmed-37894472013-10-24 RNA Splicing: A New Player in the DNA Damage Response Lenzken, Silvia C. Loffreda, Alessia Barabino, Silvia M. L. Int J Cell Biol Review Article It is widely accepted that tumorigenesis is a multistep process characterized by the sequential accumulation of genetic alterations. However, the molecular basis of genomic instability in cancer is still partially understood. The observation that hereditary cancers are often characterized by mutations in DNA repair and checkpoint genes suggests that accumulation of DNA damage is a major contributor to the oncogenic transformation. It is therefore of great interest to identify all the cellular pathways that contribute to the response to DNA damage. Recently, RNA processing has emerged as a novel pathway that may contribute to the maintenance of genome stability. In this review, we illustrate several different mechanisms through which pre-mRNA splicing and genomic stability can influence each other. We specifically focus on the role of splicing factors in the DNA damage response and describe how, in turn, activation of the DDR can influence the activity of splicing factors. Hindawi Publishing Corporation 2013 2013-09-12 /pmc/articles/PMC3789447/ /pubmed/24159334 http://dx.doi.org/10.1155/2013/153634 Text en Copyright © 2013 Silvia C. Lenzken 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 Review Article
Lenzken, Silvia C.
Loffreda, Alessia
Barabino, Silvia M. L.
RNA Splicing: A New Player in the DNA Damage Response
title RNA Splicing: A New Player in the DNA Damage Response
title_full RNA Splicing: A New Player in the DNA Damage Response
title_fullStr RNA Splicing: A New Player in the DNA Damage Response
title_full_unstemmed RNA Splicing: A New Player in the DNA Damage Response
title_short RNA Splicing: A New Player in the DNA Damage Response
title_sort rna splicing: a new player in the dna damage response
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789447/
https://www.ncbi.nlm.nih.gov/pubmed/24159334
http://dx.doi.org/10.1155/2013/153634
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