id paper:paper_00928674_v137_n4_p708_Munoz
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spelling paper:paper_00928674_v137_n4_p708_Munoz2023-06-08T15:08:25Z DNA Damage Regulates Alternative Splicing through Inhibition of RNA Polymerase II Elongation CELLBIO DNA SIGNALING DNA protein p53 RNA polymerase II apoptosis article controlled study DNA damage enzyme inhibition enzyme phosphorylation gene expression genetic transcription human human cell microarray analysis priority journal RNA splicing ultraviolet irradiation Alternative Splicing Apoptosis Cell Line, Tumor Dichlororibofuranosylbenzimidazole DNA Damage Fibronectins Fluorescence Recovery After Photobleaching Humans Mutation Oligonucleotide Array Sequence Analysis Phosphorylation RNA Polymerase II Transcription, Genetic Ultraviolet Rays DNA damage induces apoptosis and many apoptotic genes are regulated via alternative splicing (AS), but little is known about the control mechanisms. Here we show that ultraviolet irradiation (UV) affects cotranscriptional AS in a p53-independent way, through the hyperphosphorylation of RNA polymerase II carboxy-terminal domain (CTD) and a subsequent inhibition of transcriptional elongation, estimated in vivo and in real time. Phosphomimetic CTD mutants not only display lower elongation but also duplicate the UV effect on AS. Consistently, nonphosphorylatable mutants prevent the UV effect. Apoptosis promoted by UV in cells lacking p53 is prevented when the change in AS of the apoptotic gene bcl-x is reverted, confirming the relevance of this mechanism. Splicing-sensitive microarrays revealed a significant overlap of the subsets of genes that have changed AS with UV and those that have reduced expression, suggesting that transcriptional coupling to AS is a key feature of the DNA-damage response. © 2009 Elsevier Inc. All rights reserved. 2009 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00928674_v137_n4_p708_Munoz http://hdl.handle.net/20.500.12110/paper_00928674_v137_n4_p708_Munoz
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic CELLBIO
DNA
SIGNALING
DNA
protein p53
RNA polymerase II
apoptosis
article
controlled study
DNA damage
enzyme inhibition
enzyme phosphorylation
gene expression
genetic transcription
human
human cell
microarray analysis
priority journal
RNA splicing
ultraviolet irradiation
Alternative Splicing
Apoptosis
Cell Line, Tumor
Dichlororibofuranosylbenzimidazole
DNA Damage
Fibronectins
Fluorescence Recovery After Photobleaching
Humans
Mutation
Oligonucleotide Array Sequence Analysis
Phosphorylation
RNA Polymerase II
Transcription, Genetic
Ultraviolet Rays
spellingShingle CELLBIO
DNA
SIGNALING
DNA
protein p53
RNA polymerase II
apoptosis
article
controlled study
DNA damage
enzyme inhibition
enzyme phosphorylation
gene expression
genetic transcription
human
human cell
microarray analysis
priority journal
RNA splicing
ultraviolet irradiation
Alternative Splicing
Apoptosis
Cell Line, Tumor
Dichlororibofuranosylbenzimidazole
DNA Damage
Fibronectins
Fluorescence Recovery After Photobleaching
Humans
Mutation
Oligonucleotide Array Sequence Analysis
Phosphorylation
RNA Polymerase II
Transcription, Genetic
Ultraviolet Rays
DNA Damage Regulates Alternative Splicing through Inhibition of RNA Polymerase II Elongation
topic_facet CELLBIO
DNA
SIGNALING
DNA
protein p53
RNA polymerase II
apoptosis
article
controlled study
DNA damage
enzyme inhibition
enzyme phosphorylation
gene expression
genetic transcription
human
human cell
microarray analysis
priority journal
RNA splicing
ultraviolet irradiation
Alternative Splicing
Apoptosis
Cell Line, Tumor
Dichlororibofuranosylbenzimidazole
DNA Damage
Fibronectins
Fluorescence Recovery After Photobleaching
Humans
Mutation
Oligonucleotide Array Sequence Analysis
Phosphorylation
RNA Polymerase II
Transcription, Genetic
Ultraviolet Rays
description DNA damage induces apoptosis and many apoptotic genes are regulated via alternative splicing (AS), but little is known about the control mechanisms. Here we show that ultraviolet irradiation (UV) affects cotranscriptional AS in a p53-independent way, through the hyperphosphorylation of RNA polymerase II carboxy-terminal domain (CTD) and a subsequent inhibition of transcriptional elongation, estimated in vivo and in real time. Phosphomimetic CTD mutants not only display lower elongation but also duplicate the UV effect on AS. Consistently, nonphosphorylatable mutants prevent the UV effect. Apoptosis promoted by UV in cells lacking p53 is prevented when the change in AS of the apoptotic gene bcl-x is reverted, confirming the relevance of this mechanism. Splicing-sensitive microarrays revealed a significant overlap of the subsets of genes that have changed AS with UV and those that have reduced expression, suggesting that transcriptional coupling to AS is a key feature of the DNA-damage response. © 2009 Elsevier Inc. All rights reserved.
title DNA Damage Regulates Alternative Splicing through Inhibition of RNA Polymerase II Elongation
title_short DNA Damage Regulates Alternative Splicing through Inhibition of RNA Polymerase II Elongation
title_full DNA Damage Regulates Alternative Splicing through Inhibition of RNA Polymerase II Elongation
title_fullStr DNA Damage Regulates Alternative Splicing through Inhibition of RNA Polymerase II Elongation
title_full_unstemmed DNA Damage Regulates Alternative Splicing through Inhibition of RNA Polymerase II Elongation
title_sort dna damage regulates alternative splicing through inhibition of rna polymerase ii elongation
publishDate 2009
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00928674_v137_n4_p708_Munoz
http://hdl.handle.net/20.500.12110/paper_00928674_v137_n4_p708_Munoz
_version_ 1768542590601265152