Yue Yuan, Yang Yun, Dai Lanzhi, Cao Guozheng, Chen Ran, Hong Weiling, Liu Baoping, Shi Yang, Meng Yijun, Shi Feng, Xiao Mu, Jin Yongfeng
Institute of Biochemistry, College of Life Sciences, Zhejiang University (Zijingang Campus), Hangzhou, Zhejiang, ZJ310058, China.
Institute of Life Sciences, Zhejiang University (Zijingang Campus), Hangzhou, Zhejiang, ZJ310058, China.
RNA. 2016 Jan;22(1):96-110. doi: 10.1261/rna.053314.115. Epub 2015 Nov 9.
Mutually exclusive splicing is an important means of increasing the protein repertoire, by which the Down's syndrome cell adhesion molecule (Dscam) gene potentially generates 38,016 different isoforms in Drosophila melanogaster. However, the regulatory mechanisms remain obscure due to the complexity of the Dscam exon cluster. Here, we reveal a molecular model for the regulation of the mutually exclusive splicing of the serpent pre-mRNA based on competition between upstream and downstream RNA pairings. Such dual RNA pairings confer fine tuning of the inclusion of alternative exons. Moreover, we demonstrate that the splicing outcome of alternative exons is mediated in relative pairing strength-correlated mode. Combined comparative genomics analysis and experimental evidence revealed similar bidirectional structural architectures in exon clusters 4 and 9 of the Dscam gene. Our findings provide a novel mechanistic framework for the regulation of mutually exclusive splicing and may offer potentially applicable insights into long-range RNA-RNA interactions in gene regulatory networks.
相互排斥剪接是增加蛋白质组的一种重要方式,通过这种方式,唐氏综合征细胞粘附分子(Dscam)基因在黑腹果蝇中可能产生38,016种不同的异构体。然而,由于Dscam外显子簇的复杂性,其调控机制仍不清楚。在此,我们基于上游和下游RNA配对之间的竞争,揭示了一种调控蛇形前体mRNA相互排斥剪接的分子模型。这种双重RNA配对赋予了对可变外显子包含的精细调控。此外,我们证明可变外显子的剪接结果是以相对配对强度相关模式介导的。结合比较基因组学分析和实验证据,揭示了Dscam基因外显子簇4和9中类似的双向结构架构。我们的发现为相互排斥剪接的调控提供了一个新的机制框架,并可能为基因调控网络中的长程RNA-RNA相互作用提供潜在的应用见解。