Azimi Mohammad, Bulat Evgeny, Weis Karsten, Mofrad Mohammad R K
Molecular Cell Biomechanics Laboratory, Departments of Bioengineering and Mechanical Engineering, Graduate Program in Chemical Biology, Berkeley, Berkeley, CA 94720.
Molecular Cell Biomechanics Laboratory, Departments of Bioengineering and Mechanical Engineering, Graduate Program in Chemical Biology, Berkeley, Berkeley, CA 94720 Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720.
Mol Biol Cell. 2014 Nov 5;25(22):3643-53. doi: 10.1091/mbc.E14-06-1065. Epub 2014 Sep 24.
mRNA export from the nucleus is an essential step in the expression of every protein- coding gene in eukaryotes, but many aspects of this process remain poorly understood. The density of export receptors that must bind an mRNA to ensure export, as well as how receptor distribution affects transport dynamics, is not known. It is also unclear whether the rate-limiting step for transport occurs at the nuclear basket, in the central channel, or on the cytoplasmic face of the nuclear pore complex. Using previously published biophysical and biochemical parameters of mRNA export, we implemented a three-dimensional, coarse-grained, agent-based model of mRNA export in the nanosecond regime to gain insight into these issues. On running the model, we observed that mRNA export is sensitive to the number and distribution of transport receptors coating the mRNA and that there is a rate-limiting step in the nuclear basket that is potentially associated with the mRNA reconfiguring itself to thread into the central channel. Of note, our results also suggest that using a single location-monitoring mRNA label may be insufficient to correctly capture the time regime of mRNA threading through the pore and subsequent transport. This has implications for future experimental design to study mRNA transport dynamics.
在真核生物中,信使核糖核酸(mRNA)从细胞核输出是每个蛋白质编码基因表达过程中的关键步骤,但这一过程的许多方面仍知之甚少。为确保mRNA输出而必须与之结合的输出受体的密度,以及受体分布如何影响运输动力学,目前尚不清楚。同样不清楚的是,运输的限速步骤是发生在核篮、中央通道还是核孔复合体的细胞质面上。利用先前发表的mRNA输出的生物物理和生化参数,我们构建了一个三维、粗粒度、基于代理的纳秒级mRNA输出模型,以深入了解这些问题。运行该模型时,我们观察到mRNA输出对覆盖mRNA的运输受体的数量和分布敏感,并且在核篮中存在一个限速步骤,这可能与mRNA自身重新配置以穿入中央通道有关。值得注意的是,我们的结果还表明,使用单一的定位监测mRNA标签可能不足以正确捕捉mRNA穿过核孔及后续运输的时间进程。这对未来研究mRNA运输动力学的实验设计具有启示意义。