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Can we always sweep the details of RNA-processing under the carpet?

机译:我们能否始终在地毯下扫一扫RNA处理的细节?

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RNA molecules follow a succession of enzyme-mediated processing steps from transcription to maturation. The participating enzymes, for example the spliceosome for mRNAs and Drosha and Dicer for microRNAs, are also produced in the cell and their copy-numbers fluctuate over time. Enzyme copy-number changes affect the processing rate of the substrate molecules; high enzyme numbers increase the processing rate, while low enzyme numbers decrease it. We study different RNA-processing cascades where enzyme copy-numbers are either fixed or fluctuate. We find that for the fixed enzyme copy-numbers, the substrates at steady-state are Poisson-distributed, and the whole RNA cascade dynamics can be understood as a single birth-death process of the mature RNA product. In this case, solely fluctuations in the timing of RNA processing lead to variation in the number of RNA molecules. However, we show analytically and numerically that when enzyme copy-numbers fluctuate, the strength of RNA fluctuations increases linearly with the RNA transcription rate. This linear effect becomes stronger as the speed of enzyme dynamics decreases relative to the speed of RNA dynamics. Interestingly, we find that under certain conditions, the RNA cascade can reduce the strength of fluctuations in the expression level of the mature RNA product. Finally, by investigating the effects of processing polymorphisms, we show that it is possible for the effects of transcriptional polymorphisms to be enhanced, reduced or even reversed. Our results provide a framework to understand the dynamics of RNA processing.
机译:RNA分子遵循从转录到成熟的一系列酶介导的加工步骤。参与的酶,例如mRNA的剪接体和microRNA的Drosha和Dicer也产生于细胞中,它们的拷贝数会随时间波动。酶拷贝数的变化会影响底物分子的加工速度;高酶数会提高加工速度,而低酶数会降低加工速度。我们研究了不同的RNA处理级联,其中酶的拷贝数是固定的或波动的。我们发现,对于固定的酶拷贝数,稳定状态的底物是泊松分布的,整个RNA级联动力学可以理解为成熟RNA产物的一次生死过程。在这种情况下,仅RNA处理时间的波动会导致RNA分子数量的变化。但是,我们通过分析和数字显示,当酶的拷贝数波动时,RNA波动的强度随RNA转录速率线性增加。随着酶动力学速度相对于RNA动力学速度的降低,这种线性效应变得更强。有趣的是,我们发现在一定条件下,RNA级联可以降低成熟RNA产物表达水平的波动强度。最后,通过研究加工多态性的作用,我们表明转录多态性的作用有可能被增强,降低甚至逆转。我们的结果提供了一个框架,以了解RNA加工的动力学。

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