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In vivo kinetics of U4/U6?U5 tri-snRNP formation in Cajal bodies

机译:在U4 / U6的体内动力学中,在CAJAL机构中形成U5 TRI-SNRNP形成

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The U4/U6?U5 tri-small nuclear ribonucleoprotein particle (tri-snRNP) is an essential pre-mRNA splicing factor, which is assembled in a stepwise manner before each round of splicing. It was previously shown that the tri-snRNP is formed in Cajal bodies (CBs), but little is known about the dynamics of this process. Here we created a mathematical model of tri-snRNP assembly in CBs and used it to fit kinetics of individual snRNPs monitored by fluorescence recovery after photobleaching. A global fitting of all kinetic data determined key reaction constants of tri-snRNP assembly. Our model predicts that the rates of di-snRNP and tri-snRNP assemblies are similar and that ~230 tri-snRNPs are assembled in one CB per minute. Our analysis further indicates that tri-snRNP assembly is approximately 10-fold faster in CBs than in the surrounding nucleoplasm, which is fully consistent with the importance of CBs for snRNP formation in rapidly developing biological systems. Finally, the model predicted binding between SART3 and a CB component. We tested this prediction by F?rster resonance energy transfer and revealed an interaction between SART3 and coilin in CBs.
机译:U4 / U6?U5三小核核糖蛋白颗粒(三-SnRNP)是必需的前mRNA剪接因子,在每一轮拼接之前以逐步的方式组装。先前表明,三-SnRNP形成在Cajal体(CBS)中形成,但关于该过程的动态知之甚少。在这里,我们在CBS中创建了一种TRI-SNRNP组件的数学模型,并用它来适用于光漂白后通过荧光恢复监测的单个SNRNP的动力学。全局拟合三-SNRNP组件的所有动力学数据确定的关键反应常数。我们的模型预测DI-SNRNP和TRI-SNRNP组件的速率相似,〜230三SNRNPS每分钟组装在一个CB中。我们的分析进一步表明,CBS中的三-SNRNP组件比在周围的核状物中大约10倍,这与CBS在快速发展的生物系统中的SNRNP形成的重要性完全一致。最后,模型预测SART3和CB组件之间的绑定。我们通过F?RSTER共振能量转移测试了这一预测,并揭示了CBS中SART3和CO.CICIN之间的相互作用。

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