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Nuclear export of single native mRNA molecules observed by light sheet fluorescence microscopy

机译:光片荧光显微镜观察单个天然mRNA分子的核输出

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摘要

Nuclear export of mRNA is a key transport process in eukaryotic cells. To investigate it, we labeled native mRNP particles in living Chironomus tentans salivary gland cells with fluorescent hrp36, the hnRNP A1 homolog, and the nuclear envelope by fluorescent NTF2. Using light sheet microscopy, we traced single native mRNA particles across the nuclear envelope. The particles were observed to often probe nuclear pore complexes (NPC) at their nuclear face, and in only 25% of the cases yielded actual export. The complete export process took between 65 ms up to several seconds. A rate-limiting step was observed, which could be assigned to the nuclear basket of the pore and might correspond to a repositioning and unfolding of mRNPs before the actual translocation. Analysis of single fluorescent DbpB molecules, the RNA helicase essential for mRNA export, revealed that Dbp5 most often approached the cytoplasmic face of the NPC, and exhibited a binding duration of approximately 55 ms. Our results have allowed a refinement of the current models for mRNA export.
机译:mRNA的核输出是真核细胞中的关键运输过程。为了对其进行研究,我们用荧光hrp36,hnRNP A1同源物和荧光NTF2标记了活的中华绒螯蟹唾液腺细胞中的天然mRNP颗粒。使用光片显微镜,我们追踪了整个核膜的单个天然mRNA颗粒。据观察,这些颗粒经常在其核面上探测核孔复合物(NPC),只有25%的情况产生了实际出口。整个导出过程耗时65毫秒至几秒钟。观察到限速步骤,其可以分配给孔的核篮,并且可能对应于在实际移位之前mRNP的重新定位和展开。分析单个荧光DbpB分子,这是mRNA输出必不可少的RNA解旋酶,发现Dbp5最常接近NPC的细胞质表面,并表现出约55毫秒的结合时间。我们的结果使目前的mRNA出口模型得以完善。

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