Wahba Amy, Ryan Michael C, Shankavaram Uma T, Camphausen Kevin, Tofilon Philip J
Radiation Oncology Branch, National Cancer Institute, Bethesda, MD 20892, USA.
In Silico Solutions, Falls Church, VA 22043, USA.
Oncotarget. 2017 Oct 9;9(1):691-705. doi: 10.18632/oncotarget.21672. eCollection 2018 Jan 2.
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.
可变剪接是基因表达转录后调控中的一个关键事件。为了研究这一过程是否影响辐射诱导的基因表达,我们确定了电离辐射对人胶质母细胞瘤干细胞样细胞系NSC11的总细胞mRNA(转录组)和多核糖体结合mRNA(翻译组)中可变转录本生成的影响。在这些研究中,使用SpliceSeq程序比较了对照细胞和辐照细胞的RNA-Seq图谱,以识别由辐射诱导的转录本和剪接变异。与未处理细胞的转录组(总RNA)相比,辐射诱导的转录组包含92个剪接事件,表明辐射诱导了可变剪接。与未处理细胞的翻译组(多核糖体结合RNA)相比,辐射诱导的翻译组包含280个剪接事件,其中只有24个与辐射诱导的转录组重叠。这些结果表明,辐射不仅改变了前体mRNA的可变剪接,还导致了现有mRNA异构体与多核糖体的选择性结合。将辐射诱导的可变转录本与总RNA中辐射诱导的基因表达进行比较,发现重叠很少(约3%)。相反,在辐射诱导的翻译组中,约38%的诱导可变转录本对应于其表达水平在翻译组中受到影响的基因。这项研究表明,虽然辐射诱导可变剪接,但照射时存在的可变转录本可能在辐射诱导的基因表达翻译控制以及细胞辐射反应中发挥作用。