首页> 外文期刊>Plant and cell physiology >Identification of Alternative Splicing Events Regulated by an Arabidopsis Serine/Arginine-Like Protein, atSR45a, in Response to High-Light Stress using a Tiling Array
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Identification of Alternative Splicing Events Regulated by an Arabidopsis Serine/Arginine-Like Protein, atSR45a, in Response to High-Light Stress using a Tiling Array

机译:使用切片阵列,确定拟南芥丝氨酸/精氨酸样蛋白atSR45a调控的选择性剪接事件,以响应强光胁迫

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摘要

We have demonstrated that an Arabidopsis serine/arginine rich-like protein, atSR45a, interacts with other splicing factors and its expression is markedly induced by high-light stress, suggesting the involvement of atSR45a in the regulation of stress-responsive alternative splicing. A whole-genome tiling array identified the alternative splicing of genes regulated by atSR45a by comparing gene expression profiles in wild-type and knockout atSR45a (KO-sr45a) plants under high-light stress. The expression levels of genomic regions within 217 genes were significantly altered in the KO-sr45a plants compared with the wild-type plants. Many genes encoded factors involved in signal transduction, cell cycle and DNA processing, protein fate and transcription. A semi-quantitative reverse transcription-PCR (RT-PCR) analysis confirmed changes in the transcript levels and/or alternative splicing efficiency under high-light stress in 18 genes, suggesting that atSR45a affects directly or indirectly not only alternative splicing efficiency but also the transcription of these target genes. Changes in the expression of atSR45a in response to high-light stress temporally correlated with changes in the alternative splicing efficiency and transcript levels of three and one target genes, respectively. Sequencing of the alternatively spliced variants of three target genes showed that atSR45a suppresses the splicing efficiency of intron retention-type alternative splicing events. These findings indicated the importance of atSR45a to the diversification of the transcriptome under high-light stress.
机译:我们已经证明,拟南芥富含丝氨酸/精氨酸的样蛋白atSR45a与其他剪接因子相互作用,并且其表达明显受到强光诱导,表明atSR45a参与了对应激反应性替代剪接的调控。通过比较野生型和敲除atSR45a(KO-sr45a)植物在高光胁迫下的基因表达谱,全基因组切片阵列确定了atSR45a调控的基因的可变剪接。与野生型植物相比,KO-sr45a植物中217个基因内的基因组区域的表达水平发生了显着变化。许多基因编码参与信号转导,细胞周期和DNA加工,蛋白质命运和转录的因子。半定量逆转录-PCR(RT-PCR)分析确认了18个基因在强光胁迫下的转录水平和/或替代剪接效率发生了变化,这表明atSR45a不仅直接或间接影响替代剪接效率,而且还影响这些靶基因的转录。响应强光胁迫,atSR45a表达的变化与三个和一个靶基因的选择性剪接效率和转录水平的变化在时间上相关。三个靶基因的可变剪接变体的测序表明,atSR45a抑制内含子保留型可变剪接事件的剪接效率。这些发现表明在高光胁迫下atSR45a对于转录组多样化的重要性。

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