Mu Li, Hou Yan, Hu Yan, Wang Yingzhi, Shen Congcong, Luo Yongbo, Su Dan, Zhang Rundong
Department of Ophthalmology, West China Hospital, Sichuan University, Chengdu 610041, P.R. China.
State Key Laboratory of Biotherapy and Collaborative Innovation Center for Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, P.R. China.
Nucleic Acids Res. 2025 May 22;53(10). doi: 10.1093/nar/gkaf451.
Eukaryotes harbor both Sm-type and Lsm-type heteroheptameric rings, which are essential in RNA metabolism. Despite their similar subunits and evolutionary ties, they interact with RNA in distinct ways, functioning as scaffolds and chaperones, respectively. However, the mechanistic basis of their evolutionary divergence remains unclear. Using the Sm ring (D1-D2-F-E-G-D3-B) and the Lsm2-8 ring, both of which form the cores of distinct spliceosomal snRNPs, as model systems, we investigated the feasibility and mechanisms of their interconversion. We found that the interactions among subcomplexes (SCs) 1-3 in the Sm ring (D1/D2, F/E/G, and D3/B) differ from those in Lsm2-8 (Lsm2/3, Lsm6/5/7, and Lsm8/4), implying the formation of distinct assembly intermediates. By strengthening the SC1-SC3 interaction, we achieved the conversion of the Sm ring into an Lsm-type ring. Conversely, increasing the SC2-SC3 affinity did not yield a successful conversion. Furthermore, by weakening the SC1-SC3 interaction and introducing mutations in the RNA-binding regions of SC1 and SC2, we converted Lsm2-8 into a Sm-type ring. These findings provide mechanistic insights into how similar protein components can assemble into functionally distinct heteroheptameric rings, a principle likely applicable to Lsm1-7 and the U7 snRNP core, and offer deep insights into spliceosome and eukaryotic evolution.
真核生物含有Sm型和Lsm型异源七聚体环,它们在RNA代谢中至关重要。尽管它们的亚基相似且有进化关联,但它们与RNA的相互作用方式不同,分别起支架和伴侣的作用。然而,它们进化分歧的机制基础仍不清楚。我们以Sm环(D1-D2-F-E-G-D3-B)和Lsm2-8环作为模型系统,这两者都形成不同剪接体snRNP的核心,研究了它们相互转化的可行性和机制。我们发现Sm环(D1/D2、F/E/G和D3/B)中1-3亚复合物(SC)之间的相互作用与Lsm2-8(Lsm2/3、Lsm6/5/7和Lsm8/4)中的不同,这意味着形成了不同的组装中间体。通过加强SC1-SC3相互作用,我们实现了Sm环向Lsm型环的转化。相反,增加SC2-SC3亲和力并未成功实现转化。此外,通过减弱SC1-SC3相互作用并在SC1和SC2的RNA结合区域引入突变,我们将Lsm2-8转化为Sm型环。这些发现为相似的蛋白质成分如何组装成功能不同的异源七聚体环提供了机制上的见解,这一原理可能适用于Lsm1-7和U7 snRNP核心,并为剪接体和真核生物进化提供了深刻见解。