Department of NMR-based Structural Biology, Group Systems Biology of Motor Proteins, Max-Planck-Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Göttingen, Germany.
Nat Commun. 2013;4:2460. doi: 10.1038/ncomms3460.
Mutually exclusive splicing is an important mechanism in a wide range of eukaryotic branches to expand proteome diversity, but the extent of its distribution within a single species and its evolutionary conservation is unknown. Here we present a genome-wide analysis of mutually exclusive spliced exons (MXEs) in Drosophila melanogaster at unprecedented depth. Most of the new MXE candidates are supported by evolutionary conservation, transcriptome data analysis and identification of competing RNA secondary structural elements. The enrichment of the genes with MXEs in transmembrane transporters and ion channel activity is consistent with findings in humans, although the MXEs appeared independently and in non-homologous genes, supporting the idea of a universal benefit of adapting ion channel and receptor properties by tandem exon duplications. The comparison of the mutually exclusive spliced exomes within the Drosophila clade shows high numbers of MXE gain and loss events, suggesting a role of these processes in speciation.
互斥剪接是真核生物中广泛存在的一种重要机制,可扩大蛋白质组的多样性,但在单一物种内的分布程度及其进化保守性尚不清楚。本文以前所未有的深度对黑腹果蝇中的互斥剪接外显子(MXE)进行了全基因组分析。大多数新的 MXE 候选者都得到了进化保守性、转录组数据分析和竞争 RNA 二级结构元件鉴定的支持。富含 MXE 的基因在跨膜转运蛋白和离子通道活性中富集,这与人类的发现一致,尽管 MXE 是独立且在非同源基因中出现的,这支持了通过串联外显子重复来适应离子通道和受体特性的普遍益处的观点。在果蝇支系内比较互斥剪接的外显子组显示出大量的 MXE 获得和丢失事件,表明这些过程在物种形成中起作用。