Dong Haiyang, Xu Bingbing, Guo Pengjuan, Zhang Jian, Yang Xi, Li Lei, Fu Ying, Shi Jilong, Zhang Shixin, Zhu Yanda, Shi Yang, Zhou Fengyan, Bian Lina, You Wendong, Shi Feng, Yang Xiaofeng, Huang Jianhua, He Haihuai, Jin Yongfeng
MOE Laboratory of Biosystems Homeostasis & Protection and Innovation Center for Cell Signaling Network, College of Life Sciences, Zhejiang University, Hangzhou, China.
Department of Neurosurgery and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu China.
Sci Adv. 2022 Jan 28;8(4):eabm1763. doi: 10.1126/sciadv.abm1763. Epub 2022 Jan 26.
encodes 38,016 isoforms via mutually exclusive splicing; however, the regulatory mechanism behind this is not fully understood. Here, we found a set of hidden RNA secondary structures that balance the stochastic choice of splice variants (designated balancer RNA secondary structures). In vivo mutational analyses revealed the dual function of these balancer interactions in driving the stochastic choice of splice variants, through enhancement of the inclusion of distal exon 6s by cooperating with docking site-selector pairing to form a stronger multidomain pre-mRNA structure and through simultaneous repression of the inclusion of proximal exon 6s by antagonizing their docking site-selector pairings. Thus, we provide an elegant molecular model based on competition and cooperation between two sets of docking site-selector and balancer pairings, which counteracts the "first-come, first-served" principle. Our findings provide conceptual and mechanistic insight into the dynamics and functions of long-range RNA secondary structures.
通过相互排斥剪接编码38,016种异构体;然而,其背后的调控机制尚未完全明确。在此,我们发现了一组隐藏的RNA二级结构,它们平衡了剪接变体的随机选择(称为平衡子RNA二级结构)。体内突变分析揭示了这些平衡子相互作用在驱动剪接变体随机选择中的双重功能,即通过与对接位点选择器配对协作以增强远端外显子6的包含,从而形成更强的多结构域前体mRNA结构,同时通过拮抗近端外显子6的对接位点选择器配对来抑制其包含。因此,我们基于两组对接位点选择器和平衡子配对之间的竞争与合作提供了一个精妙的分子模型,该模型抵消了“先到先得”原则。我们的研究结果为远程RNA二级结构的动力学和功能提供了概念性和机制性的见解。