MOE Laboratory of Biosystems Homeostasis and Protection and Innovation Center for Cell Signaling Network, College of Life Sciences, Zhejiang University, Hangzhou, Zhejiang, ZJ310058, China.
RNA. 2020 Sep;26(9):1086-1093. doi: 10.1261/rna.075259.120. Epub 2020 May 29.
The gene potentially generates 38,016 distinct isoforms via mutually exclusive splicing, which are required for both nervous and immune functions. However, the mechanism underlying splicing regulation remains obscure. Here we show apparent evolutionary signatures characteristic of competing RNA secondary structures in exon clusters 6 and 9 of in the two midge species ( and ). Surprisingly, midge encodes only ∼6000 different isoforms through mutually exclusive splicing. Strikingly, the docking site of the exon 6 cluster is conserved in almost all insects and crustaceans but is specific in the midge; however, the docking site-selector base-pairings are conserved. Moreover, the docking site is complementary to all predicted selector sequences downstream from every variable exon 9 of the midge , which is in accordance with the broad spectrum of their isoform expression. This suggests that these -elements mainly function through the formation of long-range base-pairings. This study provides a vital insight into the evolution and mechanism of alternative splicing.
该基因通过相互排斥的剪接可能产生 38016 种独特的异构体,这些异构体对于神经和免疫功能都是必需的。然而,剪接调控的机制仍然不清楚。在这里,我们展示了在两个摇蚊物种( 和 )中第 6 和 9 外显子簇中具有竞争 RNA 二级结构特征的明显进化特征。令人惊讶的是,摇蚊 通过相互排斥的剪接仅编码约 6000 种不同的异构体。引人注目的是,外显子 6 簇的对接位点在几乎所有的昆虫和甲壳动物中都是保守的,但在摇蚊中是特异的;然而,对接位点选择碱基对是保守的。此外,对接位点与摇蚊 所有可变外显子 9 的下游所有预测选择序列互补,这与它们广泛的异构体表达一致。这表明这些 - 元件主要通过形成长距离碱基配对起作用。本研究为 可变剪接的进化和机制提供了重要的见解。