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Hidden RNA pairings counteract the “first-come, first-served” splicing principle to drive stochastic choice in Dscam1 splice variants

Drosophila melanogaster Dscam1 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 Dscam1 splice variants (designated balancer RNA...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791459/
https://www.ncbi.nlm.nih.gov/pubmed/35080968
http://dx.doi.org/10.1126/sciadv.abm1763
Descripción
Sumario:Drosophila melanogaster Dscam1 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 Dscam1 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.