Blake William J, KAErn Mads, Cantor Charles R, Collins J J
Center for BioDynamics, Center for Advanced Biotechnology, Bioinformatics Program, and Department of Biomedical Engineering, Boston University, 44 Cummington Street, Boston, Massachusetts 02215, USA.
Nature. 2003 Apr 10;422(6932):633-7. doi: 10.1038/nature01546.
Transcription in eukaryotic cells has been described as quantal, with pulses of messenger RNA produced in a probabilistic manner. This description reflects the inherently stochastic nature of gene expression, known to be a major factor in the heterogeneous response of individual cells within a clonal population to an inducing stimulus. Here we show in Saccharomyces cerevisiae that stochasticity (noise) arising from transcription contributes significantly to the level of heterogeneity within a eukaryotic clonal population, in contrast to observations in prokaryotes, and that such noise can be modulated at the translational level. We use a stochastic model of transcription initiation specific to eukaryotes to show that pulsatile mRNA production, through reinitiation, is crucial for the dependence of noise on transcriptional efficiency, highlighting a key difference between eukaryotic and prokaryotic sources of noise. Furthermore, we explore the propagation of noise in a gene cascade network and demonstrate experimentally that increased noise in the transcription of a regulatory protein leads to increased cell-cell variability in the target gene output, resulting in prolonged bistable expression states. This result has implications for the role of noise in phenotypic variation and cellular differentiation.
真核细胞中的转录被描述为量子化的,信使核糖核酸(mRNA)以概率方式产生脉冲。这种描述反映了基因表达固有的随机性,已知这是克隆群体中单个细胞对诱导刺激产生异质性反应的主要因素。我们在此表明,在酿酒酵母中,转录产生的随机性(噪声)对真核克隆群体内的异质性水平有显著贡献,这与原核生物中的观察结果不同,并且这种噪声可以在翻译水平上进行调节。我们使用特定于真核生物的转录起始随机模型表明,通过重新起始产生的脉冲式mRNA生成对于噪声对转录效率的依赖性至关重要,突出了真核生物和原核生物噪声来源之间的关键差异。此外,我们探索了噪声在基因级联网络中的传播,并通过实验证明调节蛋白转录中增加的噪声会导致靶基因输出中细胞间变异性增加,从而导致双稳态表达状态延长。这一结果对噪声在表型变异和细胞分化中的作用具有启示意义。