Department of Biochemistry, University of Wisconsin-Madison, 433 Babcock Dr., Madison, WI 53706, USA.
Department of Biochemistry, University of Wisconsin-Madison, 433 Babcock Dr., Madison, WI 53706, USA.
J Mol Biol. 2018 Feb 16;430(4):524-536. doi: 10.1016/j.jmb.2017.10.021. Epub 2017 Oct 24.
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 Förster 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 or the U2 protein Cus2; however, when Mg 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.
在酵母中,剪接体的 U2 小核 RNA(snRNA)成分会针对细胞应激做出额外的转录后修饰。在营养缺乏时,U56 和 U93 都被修饰成假尿嘧啶(Ψ),而 U56 在热休克时也被假尿嘧啶化。这两个位置都位于茎 II 内,在剪接过程中必须在两个相互排斥的结构之间切换。茎 IIa 在剪接体组装过程中形成,茎 IIc 在催化步骤中形成。我们研究了尿嘧啶 56 和 93 假尿嘧啶化如何影响茎 II 的构象转换。使用单分子Förster 共振能量转移,我们表明 Ψ56 抑制了茎 II 的构象动力学并稳定了茎 IIc。相比之下,Ψ93 增加了非茎 IIc 构象的动力学。假尿嘧啶化通过 Mg 或 U2 蛋白 Cus2 影响茎 II 的构象转换;然而,当 Mg 和 Cus2 联合使用时,假尿嘧啶化的影响可以被抑制。这些结果表明,应激诱导的 U56 和 U93 的转录后修饰通过不同的机制改变了 snRNA 的构象动力学,剪接体的蛋白质和金属辅助因子改变了 snRNA 对这些修饰的反应方式。