Permutational analysis of Saccharomyces cerevisiae regulatory elements.

IF 2.6 Q2 BIOCHEMICAL RESEARCH METHODS Synthetic biology (Oxford, England) Pub Date : 2020-01-01 Epub Date: 2020-06-16 DOI:10.1093/synbio/ysaa007
Namrita Dhillon, Robert Shelansky, Brent Townshend, Miten Jain, Hinrich Boeger, Drew Endy, Rohinton Kamakaka
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引用次数: 10

Abstract

Gene expression in Saccharomyces cerevisiae is regulated at multiple levels. Genomic and epigenomic mapping of transcription factors and chromatin factors has led to the delineation of various modular regulatory elements-enhancers (upstream activating sequences), core promoters, 5' untranslated regions (5' UTRs) and transcription terminators/3' untranslated regions (3' UTRs). However, only a few of these elements have been tested in combinations with other elements and the functional interactions between the different modular regulatory elements remain under explored. We describe a simple and rapid approach to build a combinatorial library of regulatory elements and have used this library to study 26 different enhancers, core promoters, 5' UTRs and transcription terminators/3' UTRs to estimate the contribution of individual regulatory parts in gene expression. Our combinatorial analysis shows that while enhancers initiate gene expression, core promoters modulate the levels of enhancer-mediated expression and can positively or negatively affect expression from even the strongest enhancers. Principal component analysis (PCA) indicates that enhancer and promoter function can be explained by a single principal component while UTR function involves multiple functional components. The PCA also highlights outliers and suggest differences in mechanisms of regulation by individual elements. Our data also identify numerous regulatory cassettes composed of different individual regulatory elements that exhibit equivalent gene expression levels. These data thus provide a catalog of elements that could in future be used in the design of synthetic regulatory circuits.

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酿酒酵母调控元件的排列分析。
酿酒酵母的基因表达在多个水平上受到调控。转录因子和染色质因子的基因组和表观基因组定位导致了各种模块化调控元件的描述-增强子(上游激活序列),核心启动子,5'非翻译区(5' UTRs)和转录终止子/3'非翻译区(3' UTRs)。然而,只有少数这些元素已经与其他元素组合进行了测试,不同模块调节元素之间的功能相互作用仍在探索中。我们描述了一种简单而快速的方法来构建调控元件组合文库,并利用该文库研究了26种不同的增强子、核心启动子、5' UTRs和转录终止子/3' UTRs,以估计单个调控部分在基因表达中的贡献。我们的组合分析表明,当增强子启动基因表达时,核心启动子调节增强子介导的表达水平,甚至可以对最强的增强子的表达产生积极或消极的影响。主成分分析表明,增强子和启动子功能可以用一个主成分来解释,而UTR功能则涉及多个功能成分。PCA还强调了异常值,并提出了个体要素调节机制的差异。我们的数据还确定了许多由不同个体调控元件组成的调控盒,它们表现出相同的基因表达水平。因此,这些数据提供了将来可用于合成调节电路设计的元件目录。
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