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首页> 外文期刊>Journal of Molecular Biology >Stress-induced Pseudouridylation Alters the Structural Equilibrium of Yeast U2 snRNA Stem II
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Stress-induced Pseudouridylation Alters the Structural Equilibrium of Yeast U2 snRNA Stem II

机译:应激诱导的假染蛋白改变酵母U2 snRNA茎II的结构平衡

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摘要

Abstract In yeast, the U2 small nuclear ribonucleic acid (snRNA) component of the spliceosome is targeted for additional post-transcriptional modifications in response to cellular stress. Uridines 56 and 93 are both modified to pseudouridines (Ψ) during nutrient deprivation, while U56 is also pseudouridylated during heat shock. Both positions are located within stem II, which must toggle between two mutually exclusive structures during splicing. Stem IIa forms during spliceosome assembly, and stem IIc forms during the catalytic steps. We have studied how uridine 56 and 93 pseudouridylation impacts conformational switching of stem II. Using single-molecule F?rster resonance energy transfer, we show that Ψ56 dampens conformational dynamics of stem II and stabilizes stem IIc. In contrast, Ψ93 increases dynamics of non-stem IIc conformations. Pseudouridylation impacts conformational switching of stem II by Mg 2+ or the U2 protein Cus2; however, when Mg 2+ and Cus2 are used in combination, the impacts of pseudouridylation can be suppressed. These results show that stress-induced post-transcriptional modification of U56 and U93 alters snRNA conformational dynamics by distinct mechanisms and that protein and metal cofactors of the spliceosome alter how snRNAs respond to these modifications. Graphical Abstract Display Omitted Highlights ? Pseudouridylation changes the conformational dynamics of U2 snRNA stem II. ? Pseudouridines induced under different conditions alter dynamics in distinct ways. ? Cofactors of the spliceosome suppress the impact of pseudouridylation.
机译:摘要在酵母中,抗肌肉组的U2小核核糖核酸(SnRNA)组分旨在响应细胞应激的额外转录后修饰。尿素56和93在营养剥夺期间均在缺乏症(Ⅳ)中,而U56也在热休克期间也是假约会的。两个位置位于杆II内,必须在拼接期间在两个相互排斥的结构之间切换。在抗磷酸体组装期间的干照形式,并且在催化步骤期间的茎IIC形式。我们研究了尿苷56和93假亚胺酰亚胺的影响如何影响茎II的构象切换。使用单分子F?罗斯特共振能量转移,我们展示了茎II的χ56抑制和稳定茎IIC。相比之下,ψ93增加了非茎IIC构象的动态。假染蛋白对Mg 2+或U2蛋白CUS2产生茎II的构象切换;然而,当组合使用Mg 2+和CUS2时,可以抑制假约会化的冲击。这些结果表明,U56和U93的应激诱导的转录后修饰通过不同的机制改变了SNRNA构象动态,并且抗乳糜素的蛋白质和金属辅因子改变了SNRNA如何应对这些修改。图形抽象显示省略了亮点?假染蛋白改变U2 SnRNA茎II的构象动态。还是在不同条件下诱导的假美碱以明显的方式改变动态。还是抗伤剂组的辅助膜抑制了假亚胺酰亚胺化的影响。

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