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snRNPs 与前体 mRNA 的差异相互作用揭示了活细胞中的剪接动力学。

The differential interaction of snRNPs with pre-mRNA reveals splicing kinetics in living cells.

机构信息

Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, 142 20 Prague, Czech Republic.

出版信息

J Cell Biol. 2010 Oct 4;191(1):75-86. doi: 10.1083/jcb.201004030.

Abstract

Precursor messenger RNA (pre-mRNA) splicing is catalyzed by the spliceosome, a large ribonucleoprotein (RNP) complex composed of five small nuclear RNP particles (snRNPs) and additional proteins. Using live cell imaging of GFP-tagged snRNP components expressed at endogenous levels, we examined how the spliceosome assembles in vivo. A comprehensive analysis of snRNP dynamics in the cell nucleus enabled us to determine snRNP diffusion throughout the nucleoplasm as well as the interaction rates of individual snRNPs with pre-mRNA. Core components of the spliceosome, U2 and U5 snRNPs, associated with pre-mRNA for 15-30 s, indicating that splicing is accomplished within this time period. Additionally, binding of U1 and U4/U6 snRNPs with pre-mRNA occurred within seconds, indicating that the interaction of individual snRNPs with pre-mRNA is distinct. These results are consistent with the predictions of the step-wise model of spliceosome assembly and provide an estimate on the rate of splicing in human cells.

摘要

前体信使 RNA(pre-mRNA)剪接是由剪接体催化的,剪接体是由五个小核 RNP 颗粒(snRNP)和其他蛋白质组成的大型核糖核蛋白(RNP)复合物。通过表达内源性水平的 GFP 标记的 snRNP 成分的活细胞成像,我们研究了剪接体如何在体内组装。对细胞核中 snRNP 动力学的全面分析使我们能够确定 snRNP 在核质中的扩散以及单个 snRNP 与 pre-mRNA 的相互作用速率。剪接体的核心组成部分 U2 和 U5 snRNPs 与 pre-mRNA 结合 15-30 秒,表明剪接在这段时间内完成。此外,U1 和 U4/U6 snRNPs 与 pre-mRNA 的结合发生在几秒钟内,表明单个 snRNP 与 pre-mRNA 的相互作用是不同的。这些结果与剪接体组装的逐步模型的预测一致,并提供了人细胞中剪接速率的估计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f821/2953428/ccac1ea1c633/JCB_201004030_GS_Fig1.jpg

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