Abstract

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.

Highlights

  • The development of molecularly targeted approaches for enhancing the efficacy of radiotherapy, a primary treatment modality for most solid tumors, requires a comprehensive understanding of the processes comprising cellular radioresponse

  • Radiation-induced changes in polysome-bound mRNA correlated with changes in corresponding proteins and associated cell processes supporting the concept that radiation-induced translational control of gene expression is a fundamental component of radioresponse

  • Comparison of mRNA isoforms detected in polysome-bound mRNA to those in total mRNA revealed 666 splicing events significantly enriched in the polysome-bound RNA (Figure 1A) corresponding to 567 genes (Supplementary Table 2)

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Summary

Introduction

The development of molecularly targeted approaches for enhancing the efficacy of radiotherapy, a primary treatment modality for most solid tumors, requires a comprehensive understanding of the processes comprising cellular radioresponse. To address the discrepancy between the radiation-induced transcriptome and proteome, polysome-bound RNA, which identifies www.impactjournals.com/oncotarget genes undergoing translation and defines the translatome, was subjected to microarray analysis and compared to the traditional microarray approach using total cellular mRNA [8, 9]. The results of these studies showed that the number of genes in the radiation-induced translatome was substantially greater than those in the radiation-induced transcriptome and that there was little to no overlap between the two expression profiles. Data indicate that radiation modifies gene expression primarily through translational control

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