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全基因组复制事件后CK1δ/ε激酶同源基因的平行非功能化

Parallel nonfunctionalization of CK1δ/ε kinase ohnologs following a whole-genome duplication event.

作者信息

Evans-Yamamoto Daniel, Dubé Alexandre K, Saha Gourav, Plante Samuel, Bradley David, Gagnon-Arsenault Isabelle, Landry Christian R

机构信息

Institut de Biologie Intégrative et des Systèmes (IBIS), Université Laval, G1V 0A6, Canada.

Département de Biochimie, de Microbiologie et de Bio-informatique, Faculté des Sciences et de Génie, Université Laval, G1V 0A6, Canada.

出版信息

bioRxiv. 2023 Oct 2:2023.10.02.560513. doi: 10.1101/2023.10.02.560513.

Abstract

Whole genome duplication (WGD) followed by speciation allows us to examine the parallel evolution of ohnolog pairs. In the yeast family , is a rare case of repeated ohnolog maintenance. This gene has reverted to a single copy in where it is now essential, but has been maintained as pairs in at least 7 species post WGD. In , encodes the casein kinase (CK) 1δ/ε and plays a role in a variety of functions through its kinase activity and protein-protein interactions (PPIs). We hypothesized that the maintenance of duplicated ohnologs could be a result of repeated subfunctionalization. We tested this hypothesis through a functional complementation assay in , testing all pairwise combinations of 25 orthologs (including 7 ohnolog pairs). Contrary to our expectations, we observed no cases of pair-dependent complementation, which would have supported the subfunctionalization hypothesis. Instead, most post-WGD species have one ohnolog that failed to complement, suggesting their nonfunctionalization or neofunctionalization. The ohnologs incapable of complementation have undergone more rapid protein evolution, lost most PPIs that were observed for their functional counterparts and singletons from post and non-WGD species, and have non-conserved cellular localization, consistent with their ongoing loss of function. The analysis in shows that the non-complementing ohnolog is expressed at a lower level and has become non-essential. Taken together, our results indicate that orthologs are undergoing gradual nonfunctionalization.

摘要

全基因组复制(WGD)后紧接着物种形成,这使我们能够研究ohnolog基因对的平行进化。在酵母家族中,[具体基因名称未给出]是重复的ohnolog维持的罕见案例。该基因在[具体物种名称未给出]中已恢复为单拷贝,在那里它现在是必需的,但在WGD后的至少7个物种中一直以基因对的形式存在。在[具体物种名称未给出]中,[具体基因名称未给出]编码酪蛋白激酶(CK)1δ/ε,并通过其激酶活性和蛋白质 - 蛋白质相互作用(PPI)在多种功能中发挥作用。我们假设重复的ohnolog基因对的维持可能是重复亚功能化的结果。我们通过在[具体物种名称未给出]中的功能互补试验来检验这一假设,测试了25个直系同源基因的所有成对组合(包括7个ohnolog基因对)。与我们的预期相反,我们没有观察到支持亚功能化假设的成对依赖性互补的情况。相反,大多数WGD后的物种有一个未能互补的ohnolog,这表明它们发生了功能丧失或新功能化。无法互补的ohnolog经历了更快的蛋白质进化,失去了大多数在其功能对应物以及来自WGD后和非WGD物种的单拷贝基因中观察到的PPI,并且具有不保守的细胞定位,这与它们持续的功能丧失一致。在[具体物种名称未给出]中的分析表明,不互补的ohnolog表达水平较低且已变得非必需。综上所述,我们的结果表明[具体基因名称未给出]的直系同源基因正在经历逐渐的功能丧失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6386/10592909/cf51037bfa09/nihpp-2023.10.02.560513v1-f0001.jpg

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