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Diverse mechanisms for spliceosome-mediated 3′ end processing of telomerase RNA

机译:剪接体介导的端粒酶RNA 3'末端加工的多种机制

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The 3′ end of Schizosaccharomyces pombe telomerase RNA ( Sp TER1 ) is generated by spliceosomal cleavage, a reaction that corresponds to the first step of splicing. The observation that the spliceosome functions in 3′ end processing raised questions about the evolutionary origin and conservation of this mechanism. We now present data in support of spliceosomes generating 3′ ends of telomerase RNAs in other fungi. Strikingly, the mechanistic basis for restricting spliceosomal splicing to the first transesterification reaction differs substantially among species. Unlike S. pombe , two other fission yeasts rely on hyperstabilization of the U6 snRNA—5′ splice site interaction to impede the 2nd step of splicing. In contrast, a non-canonical 5′ splice site blocks the second transesterification reaction in Aspergillus species. These results demonstrate a conserved role for spliceosomes functioning in 3′ end processing. Divergent mechanisms of uncoupling the two steps of splicing argue for multiple origins of this pathway.
机译:裂殖酵母端粒酶RNA(Sp TER1)的3'端通过剪接切割产生,该反应对应于剪接的第一步。剪接体在3'末端加工中起作用的观察提出了有关该机制的进化起源和保守性的问题。现在,我们提出数据来支持在其他真菌中产生端粒酶RNAs 3'末端的剪接体。令人惊讶的是,在物种间将剪接体剪接限制在第一酯交换反应的机理基础上存在很大差异。与粟酒裂殖酵母不同,另两个裂变酵母依赖于U6 snRNA-5'剪接位点相互作用的高度稳定化来阻止第二步剪接。相反,非经典的5'剪接位点阻断了曲霉属物种中的第二次酯交换反应。这些结果证明了剪接体在3'末端加工中起作用的保守作用。解耦两个步骤的不同机制为该途径的多重起源辩解。

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