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Radiation-induced alternative transcripts as detected in total and polysome-bound mRNA

Alternative splicing is a critical event in the posttranscriptional regulation of gene expression. To investigate whether this process influences radiation-induced gene expression we defined the effects of ionizing radiation on the generation of alternative transcripts in total cellular mRNA (the tr...

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Autores principales: Wahba, Amy, Ryan, Michael C., Shankavaram, Uma T., Camphausen, Kevin, Tofilon, Philip J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787501/
https://www.ncbi.nlm.nih.gov/pubmed/29416646
http://dx.doi.org/10.18632/oncotarget.21672
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author Wahba, Amy
Ryan, Michael C.
Shankavaram, Uma T.
Camphausen, Kevin
Tofilon, Philip J.
author_facet Wahba, Amy
Ryan, Michael C.
Shankavaram, Uma T.
Camphausen, Kevin
Tofilon, Philip J.
author_sort Wahba, Amy
collection PubMed
description Alternative splicing is a critical event in the posttranscriptional regulation of gene expression. To investigate whether this process influences radiation-induced gene expression we defined the effects of ionizing radiation on the generation of alternative transcripts in total cellular mRNA (the transcriptome) and polysome-bound mRNA (the translatome) of the human glioblastoma stem-like cell line NSC11. For these studies, RNA-Seq profiles from control and irradiated cells were compared using the program SpliceSeq to identify transcripts and splice variations induced by radiation. As compared to the transcriptome (total RNA) of untreated cells, the radiation-induced transcriptome contained 92 splice events suggesting that radiation induced alternative splicing. As compared to the translatome (polysome-bound RNA) of untreated cells, the radiation-induced translatome contained 280 splice events of which only 24 were overlapping with the radiation-induced transcriptome. These results suggest that radiation not only modifies alternative splicing of precursor mRNA, but also results in the selective association of existing mRNA isoforms with polysomes. Comparison of radiation-induced alternative transcripts to radiation-induced gene expression in total RNA revealed little overlap (about 3%). In contrast, in the radiation-induced translatome, about 38% of the induced alternative transcripts corresponded to genes whose expression level was affected in the translatome. This study suggests that whereas radiation induces alternate splicing, the alternative transcripts present at the time of irradiation may play a role in the radiation-induced translational control of gene expression and thus cellular radioresponse.
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spelling pubmed-57875012018-02-07 Radiation-induced alternative transcripts as detected in total and polysome-bound mRNA Wahba, Amy Ryan, Michael C. Shankavaram, Uma T. Camphausen, Kevin Tofilon, Philip J. Oncotarget Research Paper Alternative splicing is a critical event in the posttranscriptional regulation of gene expression. To investigate whether this process influences radiation-induced gene expression we defined the effects of ionizing radiation on the generation of alternative transcripts in total cellular mRNA (the transcriptome) and polysome-bound mRNA (the translatome) of the human glioblastoma stem-like cell line NSC11. For these studies, RNA-Seq profiles from control and irradiated cells were compared using the program SpliceSeq to identify transcripts and splice variations induced by radiation. As compared to the transcriptome (total RNA) of untreated cells, the radiation-induced transcriptome contained 92 splice events suggesting that radiation induced alternative splicing. As compared to the translatome (polysome-bound RNA) of untreated cells, the radiation-induced translatome contained 280 splice events of which only 24 were overlapping with the radiation-induced transcriptome. These results suggest that radiation not only modifies alternative splicing of precursor mRNA, but also results in the selective association of existing mRNA isoforms with polysomes. Comparison of radiation-induced alternative transcripts to radiation-induced gene expression in total RNA revealed little overlap (about 3%). In contrast, in the radiation-induced translatome, about 38% of the induced alternative transcripts corresponded to genes whose expression level was affected in the translatome. This study suggests that whereas radiation induces alternate splicing, the alternative transcripts present at the time of irradiation may play a role in the radiation-induced translational control of gene expression and thus cellular radioresponse. Impact Journals LLC 2017-10-09 /pmc/articles/PMC5787501/ /pubmed/29416646 http://dx.doi.org/10.18632/oncotarget.21672 Text en Copyright: © 2018 Wahba et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Wahba, Amy
Ryan, Michael C.
Shankavaram, Uma T.
Camphausen, Kevin
Tofilon, Philip J.
Radiation-induced alternative transcripts as detected in total and polysome-bound mRNA
title Radiation-induced alternative transcripts as detected in total and polysome-bound mRNA
title_full Radiation-induced alternative transcripts as detected in total and polysome-bound mRNA
title_fullStr Radiation-induced alternative transcripts as detected in total and polysome-bound mRNA
title_full_unstemmed Radiation-induced alternative transcripts as detected in total and polysome-bound mRNA
title_short Radiation-induced alternative transcripts as detected in total and polysome-bound mRNA
title_sort radiation-induced alternative transcripts as detected in total and polysome-bound mrna
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787501/
https://www.ncbi.nlm.nih.gov/pubmed/29416646
http://dx.doi.org/10.18632/oncotarget.21672
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