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Role of the DNA Damage Response in Human Papillomavirus RNA Splicing and Polyadenylation

Human papillomaviruses (HPVs) have evolved to use the DNA repair machinery to replicate its DNA genome in differentiated cells. HPV activates the DNA damage response (DDR) in infected cells. Cellular DDR factors are recruited to the HPV DNA genome and position the cellular DNA polymerase on the HPV...

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Autores principales: Nilsson, Kersti, Wu, Chengjun, Schwartz, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032147/
https://www.ncbi.nlm.nih.gov/pubmed/29895741
http://dx.doi.org/10.3390/ijms19061735
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author Nilsson, Kersti
Wu, Chengjun
Schwartz, Stefan
author_facet Nilsson, Kersti
Wu, Chengjun
Schwartz, Stefan
author_sort Nilsson, Kersti
collection PubMed
description Human papillomaviruses (HPVs) have evolved to use the DNA repair machinery to replicate its DNA genome in differentiated cells. HPV activates the DNA damage response (DDR) in infected cells. Cellular DDR factors are recruited to the HPV DNA genome and position the cellular DNA polymerase on the HPV DNA and progeny genomes are synthesized. Following HPV DNA replication, HPV late gene expression is activated. Recent research has shown that the DDR factors also interact with RNA binding proteins and affects RNA processing. DDR factors activated by DNA damage and that associate with HPV DNA can recruit splicing factors and RNA binding proteins to the HPV DNA and induce HPV late gene expression. This induction is the result of altered alternative polyadenylation and splicing of HPV messenger RNA (mRNA). HPV uses the DDR machinery to replicate its DNA genome and to activate HPV late gene expression at the level of RNA processing.
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spelling pubmed-60321472018-07-13 Role of the DNA Damage Response in Human Papillomavirus RNA Splicing and Polyadenylation Nilsson, Kersti Wu, Chengjun Schwartz, Stefan Int J Mol Sci Review Human papillomaviruses (HPVs) have evolved to use the DNA repair machinery to replicate its DNA genome in differentiated cells. HPV activates the DNA damage response (DDR) in infected cells. Cellular DDR factors are recruited to the HPV DNA genome and position the cellular DNA polymerase on the HPV DNA and progeny genomes are synthesized. Following HPV DNA replication, HPV late gene expression is activated. Recent research has shown that the DDR factors also interact with RNA binding proteins and affects RNA processing. DDR factors activated by DNA damage and that associate with HPV DNA can recruit splicing factors and RNA binding proteins to the HPV DNA and induce HPV late gene expression. This induction is the result of altered alternative polyadenylation and splicing of HPV messenger RNA (mRNA). HPV uses the DDR machinery to replicate its DNA genome and to activate HPV late gene expression at the level of RNA processing. MDPI 2018-06-12 /pmc/articles/PMC6032147/ /pubmed/29895741 http://dx.doi.org/10.3390/ijms19061735 Text en © 2018 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Nilsson, Kersti
Wu, Chengjun
Schwartz, Stefan
Role of the DNA Damage Response in Human Papillomavirus RNA Splicing and Polyadenylation
title Role of the DNA Damage Response in Human Papillomavirus RNA Splicing and Polyadenylation
title_full Role of the DNA Damage Response in Human Papillomavirus RNA Splicing and Polyadenylation
title_fullStr Role of the DNA Damage Response in Human Papillomavirus RNA Splicing and Polyadenylation
title_full_unstemmed Role of the DNA Damage Response in Human Papillomavirus RNA Splicing and Polyadenylation
title_short Role of the DNA Damage Response in Human Papillomavirus RNA Splicing and Polyadenylation
title_sort role of the dna damage response in human papillomavirus rna splicing and polyadenylation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032147/
https://www.ncbi.nlm.nih.gov/pubmed/29895741
http://dx.doi.org/10.3390/ijms19061735
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