Jia Ya, Liu Wangheng, Li Anbang, Yang Lijian, Zhan Xuan
Department of Physics and Institute of Biophysics, Central China Normal University, Wuhan 430079, PR China.
Biophys Chem. 2009 Jul;143(1-2):60-9. doi: 10.1016/j.bpc.2009.04.001. Epub 2009 Apr 5.
Small non-coding RNA (sRNA) plays very important role in the post transcriptional regulation in various organisms. In complex regulatory networks, highly significant relative fluctuations in RNAs copy numbers can not be neglected due to very small copy number of individual RNA molecules. Here we consider two simple regulation schemes, where one is single target gene regulated by a sRNA and the other is two target mRNAs (mRNA(R) and mRNA(T)) regulated by one sRNA. The Fano factor (a measure of the relative size of the internal fluctuations) formulae of RNA molecules in the post transcriptional regulation are theoretically derived by using of the Langevin theory. For single target gene regulated by a sRNA, it is shown that the intrinsic noise of both mRNA and sRNA approaches the bare Poissonian limit in the regimen of both target RNA silencing and surviving. However, the strong anti-correlation between the fluctuations of two components result in a large intrinsic fluctuations in the level of RNA molecules in the regimen of crossover. For two target mRNAs regulated by one sRNA, in the regimen of crossover, it is found that, with the increasing of transcription rate of target mRNA(T), the maximal intrinsic fluctuation of RNA molecules is shifted from sRNA to target mRNA(R), and then to target mRNA(T). The intrinsic noise intensity of target mRNA(R) is determined by both the transcriptional rate of itself and that of sRNA, and independent of the transcriptional rate of the other target mRNA(T).
小非编码RNA(sRNA)在各种生物体的转录后调控中发挥着非常重要的作用。在复杂的调控网络中,由于单个RNA分子的拷贝数非常少,RNA拷贝数中高度显著的相对波动不容忽视。在这里,我们考虑两种简单的调控方案,一种是由一个sRNA调控单个靶基因,另一种是由一个sRNA调控两个靶mRNA(mRNA(R)和mRNA(T))。利用朗之万理论从理论上推导了转录后调控中RNA分子的法诺因子(内部波动相对大小的一种度量)公式。对于由一个sRNA调控的单个靶基因,结果表明,在靶RNA沉默和存活的情况下,mRNA和sRNA的固有噪声都接近裸泊松极限。然而,两个组分波动之间的强反相关性导致在交叉情况下RNA分子水平存在较大的固有波动。对于由一个sRNA调控的两个靶mRNA,在交叉情况下,发现随着靶mRNA(T)转录速率的增加,RNA分子的最大固有波动从sRNA转移到靶mRNA(R),然后再转移到靶mRNA(T)。靶mRNA(R)的固有噪声强度由其自身的转录速率和sRNA的转录速率共同决定,且与另一个靶mRNA(T)的转录速率无关。