Brown Christopher R, Boeger Hinrich
Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, CA 95064.
Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, CA 95064
Proc Natl Acad Sci U S A. 2014 Dec 16;111(50):17893-8. doi: 10.1073/pnas.1417527111. Epub 2014 Dec 2.
Gene product molecule numbers fluctuate over time and between cells, confounding deterministic expectations. The molecular origins of this noise of gene expression remain unknown. Recent EM analysis of single PHO5 gene molecules of yeast indicated that promoter molecules stochastically assume alternative nucleosome configurations at steady state, including the fully nucleosomal and nucleosome-free configuration. Given that distinct configurations are unequally conducive to transcription, the nucleosomal variation of promoter molecules may constitute a source of gene expression noise. This notion, however, implies an untested conjecture, namely that the nucleosomal variation arises de novo or intrinsically (i.e., that it cannot be explained as the result of the promoter's deterministic response to variation in its molecular surroundings). Here, we show--by microscopically analyzing the nucleosome configurations of two juxtaposed physically linked PHO5 promoter copies--that the configurational variation, indeed, is intrinsically stochastic and thus, a cause of gene expression noise rather than its effect.
基因产物的分子数量会随时间以及细胞之间的差异而波动,这使得确定性预期变得复杂。基因表达这种噪声的分子起源仍然未知。最近对酵母单个PHO5基因分子的电子显微镜分析表明,启动子分子在稳态下会随机呈现出不同的核小体构型,包括完全核小体化和无核小体构型。鉴于不同的构型对转录的促进作用不同,启动子分子的核小体变异可能构成基因表达噪声的一个来源。然而,这一观点意味着一个未经检验的推测,即核小体变异是从头产生或内在产生的(也就是说,它不能被解释为启动子对其分子环境变化的确定性反应的结果)。在这里,我们通过显微镜分析两个并列的物理连接的PHO5启动子拷贝的核小体构型表明,构型变异确实是内在随机的,因此,它是基因表达噪声的一个原因而非结果。