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Introns regulate the production of ribosomal proteins by modulating splicing of duplicated ribosomal protein genes

机译:内含子通过调节重复的核糖体蛋白基因的剪接来调节核糖体蛋白的产生

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Most budding yeast introns exist in the many duplicated ribosomal protein genes (RPGs) and it has been posited that they remain there to modulate the expression of RPGs and cell growth in response to stress. However, the mechanism by which introns regulate the expression of RPGs and their impact on the synthesis of ribosomal proteins remain unclear. In this study, we show that introns determine the ratio of ribosomal protein isoforms through asymmetric paralog-specific regulation of splicing. Exchanging the introns and 3' untranslated regions of the duplicated RPS9 genes altered the splicing efficiency and changed the ratio of the ribosomal protein isoforms. Mutational analysis of the RPS9 genes indicated that splicing is regulated by variations in the intron structure and the 3' untranslated region. Together these data suggest that preferential splicing of duplicated RPGs provides a means for adjusting the ratio of different ribosomal protein isoforms, while maintaining the overall expression level of each ribosomal protein.
机译:大多数发芽的酵母内含子都存在于许多重复的核糖体蛋白基因(RPG)中,并且据推测它们保留在那里以调节RPG的表达和响应压力的细胞生长。然而,内含子调节RPGs表达的机制及其对核糖体蛋白合成的影响尚不清楚。在这项研究中,我们表明内含子通过非对称的对数同源特异性剪接确定核糖体蛋白同工型的比率。交换重复的RPS9基因的内含子和3'非翻译区改变了剪接效率,并改变了核糖体蛋白同工型的比例。 RPS9基因的突变分析表明,剪接受内含子结构和3'非翻译区变化的调控。这些数据共同表明,重复的RPG的优先剪接提供了一种调节不同核糖体蛋白同工型比例的手段,同时又能维持每种核糖体蛋白的总体表达水平。

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