Differential Evolution of CDS and UTR Non-canonical RNA G-quadruplex Structures in Eukaryotic Transcriptomes.

IF 7.9
Eugene Yui-Ching Chow, Jieyu Zhao, Chun Kit Kwok, Ting-Fung Chan
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Abstract

RNA G-quadruplexes (rG4s) are non-classical, four-stranded secondary RNA structures that play regulatory roles in various biological processes. Although canonical rG4s have been studied extensively, recent advancements have underscored the importance of non-canonical rG4s. In this study, we experimentally determined rG4 structures from multiple eukaryotic species. Bioinformatic analysis revealed that across 1 billion years of evolution, rG4s have comprised an integral feature of eukaryotic transcriptomes; additionally, non-canonical rG4s consistently were found to dominate the surveyed rG4omes. Over time, the overall size of the rG4ome has expanded progressively, accompanied by a notable compositional shift such that untranslated region (UTR) rG4s became favored over protein coding-sequence (CDS) rG4s. Additionally, we observed distinct evolutionary patterns for CDS and UTR rG4s, which involved differential evolutionary origins and canonicality drift patterns. Our findings suggest that new UTR rG4 sequences emerged rapidly during early mammalian evolution, whereas the more gradual increase in CDS rG4s is linked to changes in selective amino acid residue preferences. This plausible theory accounts for both the prevalence of UTR rG4s and the emergence of canonical motifs in mammalian models. Access to all of the rG4 structures identified in this study is available through the rG4-seq Database application at https://rg4s.science/.

真核生物转录组中CDS和UTR非规范RNA g -四重体结构的差异进化
RNA g -四联体(rG4s)是一种非经典的四链二级RNA结构,在各种生物过程中发挥调控作用。尽管规范rG4s已被广泛研究,但最近的进展强调了非规范rG4s的重要性。在本研究中,我们实验测定了来自多个真核生物物种的rG4结构。生物信息学分析显示,经过10亿年的进化,rG4s已经构成了真核生物转录组的一个完整特征;此外,非规范rG4s一直被发现在调查的rg4ome中占主导地位。随着时间的推移,rG4ome的总体大小逐渐扩大,伴随着显著的组成变化,使得非翻译区(UTR) rG4s比蛋白质编码序列(CDS) rG4s更受青睐。此外,我们还观察到CDS和UTR rG4s的不同进化模式,包括差异进化起源和规范性漂移模式。我们的研究结果表明,新的UTR rG4序列在哺乳动物早期进化过程中迅速出现,而CDS rG4序列的逐渐增加与选择性氨基酸残基偏好的变化有关。这一看似合理的理论解释了哺乳动物模型中UTR rG4s的流行和规范基序的出现。通过rG4-seq数据库应用程序https://rg4s.science/可以访问本研究中确定的所有rG4结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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