Miyata Yuna, Yamagami Ryota, Kawamura Takuya, Hori Hiroyuki, Hirata Akira
Department of Natural Science, Division of Science and Technology, Graduate School of Sciences and Technology for Innovation, Tokushima University, 2-1 Minamijosanjima-cho, Tokushima, Tokushima 770-8506, Japan.
Department of Applied Chemistry, Graduate School of Science and Engineering, Ehime University, 3 Bunkyo-cho, Matsuyama, Ehime 790-8577, Japan.
Nucleic Acids Res. 2025 Aug 27;53(16). doi: 10.1093/nar/gkaf845.
Maturation of transfer RNA molecules often requires removal of intronic sequences by endonucleases that recognize diverse RNA secondary structures. Archaeal splicing endonucleases [versatile RNA-splicing endonucleases (VSENs)] exhibit remarkable substrate versatility, yet the structural basis for this broad specificity has remained unclear. Here, we report the 1.8-Å crystal structure of ARMAN-2, an ϵ2-type VSEN from Candidatus Micrarchaeum acidiphilum, in complex with a synthetic bulge-helix-bulge RNA. The structure reveals that a lineage-specific insertion, the ARMAN-specific loop (ASL), interacts with the bulged region of the RNA and helps to orient the scissile phosphate for catalysis via conserved tyrosine and lysine residues. Functional assays confirmed the essential role of the ASL in substrate binding and cleavage. Structural comparisons with (αβ)2-type Crenarchaeal VSENs, which contain a distinct Crenarchaea-specific loop (CSL), and with a eukaryotic equivalent, the TSEN complex, which harbors a previously uncharacterized eukaryotic-specific loop (ESL), uncovered mechanistic convergence across domains of life. We show that the ESL occupies a position analogous to the ASL and CSL, and likely supports bulge stabilization in long introns. These findings establish a mechanistic model for broad substrate recognition by VSENs and suggest that loop-mediated RNA positioning co-evolved with intron complexity in archaeal and eukaryotic lineages.
转运RNA分子的成熟通常需要通过识别多种RNA二级结构的核酸内切酶去除内含子序列。古菌剪接核酸内切酶[通用RNA剪接核酸内切酶(VSENs)]表现出显著的底物通用性,但其广泛特异性的结构基础仍不清楚。在这里,我们报告了来自嗜酸微小古菌的ε2型VSEN——ARMAN-2与合成的凸起-螺旋-凸起RNA复合物的1.8埃晶体结构。该结构显示,一个谱系特异性插入序列,即ARMAN特异性环(ASL),与RNA的凸起区域相互作用,并通过保守的酪氨酸和赖氨酸残基帮助将可切割磷酸定位以进行催化。功能测定证实了ASL在底物结合和切割中的关键作用。与含有独特的泉古菌特异性环(CSL)的(αβ)2型泉古菌VSEN以及与含有先前未表征的真核特异性环(ESL)的真核等同物TSEN复合物进行结构比较,揭示了生命各域之间的机制趋同。我们表明,ESL占据与ASL和CSL类似的位置,并可能在长内含子中支持凸起稳定化。这些发现建立了VSEN广泛底物识别的机制模型,并表明环介导的RNA定位与古菌和真核谱系中的内含子复杂性共同进化。