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内含子为酵母中RPL22旁系同源基因的基因间调控反馈提供了一个平台。

Introns provide a platform for intergenic regulatory feedback of RPL22 paralogs in yeast.

作者信息

Abrhámová Kateřina, Nemčko Filip, Libus Jiří, Převorovský Martin, Hálová Martina, Půta František, Folk Petr

机构信息

Department of Cell Biology, Faculty of Science, Charles University, Prague, Czech Republic.

出版信息

PLoS One. 2018 Jan 5;13(1):e0190685. doi: 10.1371/journal.pone.0190685. eCollection 2018.

Abstract

Ribosomal protein genes (RPGs) in Saccharomyces cerevisiae are a remarkable regulatory group that may serve as a model for understanding genetic redundancy in evolutionary adaptations. Most RPGs exist as pairs of highly conserved functional paralogs with divergent untranslated regions and introns. We examined the roles of introns in strains with various combinations of intron and gene deletions in RPL22, RPL2, RPL16, RPL37, RPL17, RPS0, and RPS18 paralog pairs. We found that introns inhibited the expression of their genes in the RPL22 pair, with the RPL22B intron conferring a much stronger effect. While the WT RPL22A/RPL22B mRNA ratio was 93/7, the rpl22aΔi/RPL22B and RPL22A/rpl22bΔi ratios were >99/<1 and 60/40, respectively. The intron in RPL2A stimulated the expression of its own gene, but the removal of the other introns had little effect on expression of the corresponding gene pair. Rpl22 protein abundances corresponded to changes in mRNAs. Using splicing reporters containing endogenous intron sequences, we demonstrated that these effects were due to the inhibition of splicing by Rpl22 proteins but not by their RNA-binding mutant versions. Indeed, only WT Rpl22A/Rpl22B proteins (but not the mutants) interacted in a yeast three-hybrid system with an RPL22B intronic region between bp 165 and 236. Transcriptome analysis showed that both the total level of Rpl22 and the A/B ratio were important for maintaining the WT phenotype. The data presented here support the contention that the Rpl22B protein has a paralog-specific role. The RPL22 singleton of Kluyveromyces lactis, which did not undergo whole genome duplication, also responded to Rpl22-mediated inhibition in K. lactis cells. Vice versa, the overproduction of the K. lactis protein reduced the expression of RPL22A/B in S. cerevisiae. The extraribosomal function of of the K. lactis Rpl22 suggests that the loop regulating RPL22 paralogs of S. cerevisiae evolved from autoregulation.

摘要

酿酒酵母中的核糖体蛋白基因(RPGs)是一个非凡的调控基团,可作为理解进化适应中基因冗余的模型。大多数RPGs以高度保守的功能旁系同源基因对的形式存在,其非翻译区和内含子存在差异。我们研究了RPL22、RPL2、RPL16、RPL37、RPL17、RPS0和RPS18旁系同源基因对内含子在各种内含子和基因缺失组合菌株中的作用。我们发现,内含子在RPL22基因对中抑制其基因的表达,其中RPL22B内含子的作用更强。野生型RPL22A/RPL22B mRNA比例为93/7,而rpl22aΔi/RPL22B和RPL22A/rpl22bΔi比例分别>99/<1和60/40。RPL2A中的内含子刺激其自身基因的表达,但去除其他内含子对相应基因对的表达影响不大。Rpl22蛋白丰度与mRNA的变化相对应。使用包含内源性内含子序列的剪接报告基因,我们证明这些影响是由于Rpl22蛋白对剪接的抑制,而不是其RNA结合突变体版本。实际上,只有野生型Rpl22A/Rpl22B蛋白(而非突变体)在酵母三杂交系统中与bp 165至236之间的RPL22B内含子区域相互作用。转录组分析表明,Rpl22的总水平和A/B比例对于维持野生型表型都很重要。此处提供的数据支持Rpl22B蛋白具有旁系同源基因特异性作用的观点。未经历全基因组复制的乳酸克鲁维酵母的RPL22单拷贝基因,在乳酸克鲁维酵母细胞中也对Rpl22介导的抑制有反应。反之,乳酸克鲁维酵母蛋白的过量表达降低了酿酒酵母中RPL22A/B的表达。乳酸克鲁维酵母Rpl22的核糖体外功能表明,调节酿酒酵母RPL22旁系同源基因的环是从自我调节进化而来的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7741/5755908/b953fc7a86e1/pone.0190685.g001.jpg

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