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Structural Characterization of RNA Recognition Motif‐2 Domain of SART3

机译:SART3 RNA识别Motif-2域的结构表征

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Squamous cell carcinoma antigen recognized by Ta??cells 3 (SART3) is an essential recycling factor in prea??mRNA splicing, which is required for association of U4/U6 small nuclear ribonucleoprotein (snRNP). SART3 contains two RNA recognition motifs (RRMs), and they are responsible for the tertiary interaction with U6 small nuclear RNA. Despite the importance of structural studies for understanding complicate U4/U6 snRNP recycling mechanism, only a few of them have been performed for SART3. Here, the structure of SART3 RRM2 was characterized by heteronuclear multia??dimensional nuclear magnetic resonance experiments. Nearly complete 1H, 15N, and 13C chemical shifts of the backbone residues of RRM2 were assigned. In addition, the secondary structure of RRM2 were predicted by the chemical shift index and TALOS+ analyses, and the results showed that RRM2 forms a a???21a???±1a???22a???23a???±2a???24a???25a?? structure, where ?24 is not common in the canonical RRM domain structures. Our results will provide structural basis for investigation of SART3a??mediated U4/U6 snRNP complex formation.
机译:被Taβ3细胞(SART3)识别的鳞状细胞癌抗原是preaβmRNA剪接中必不可少的循环因子,这是U4 / U6小核糖核蛋白(snRNP)缔合所必需的。 SART3包含两个RNA识别基序(RRM),它们负责与U6小核RNA的三级相互作用。尽管结构研究对于理解复杂的U4 / U6 snRNP回收机制非常重要,但其中只有少数几个是针对SART3进行的。在此,SART3 RRM2的结构通过异核多维核磁共振实验表征。 RRM2的骨架残基几乎完成了1H,15N和13C的化学位移。另外,通过化学位移指数和TALOS +分析预测了RRM2的二级结构,结果表明RRM2形成aa 21 21,±1a,22a,23a,±2a。 ?? 24a ??? 25a ??在规范的RRM域结构中,?24不常见。我们的结果将为研究SART3aβ介导的U4 / U6 snRNP复合物的形成提供结构基础。

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