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调控元件的排列分析

Permutational analysis of regulatory elements.

作者信息

Dhillon Namrita, Shelansky Robert, Townshend Brent, Jain Miten, Boeger Hinrich, Endy Drew, Kamakaka Rohinton

机构信息

Department of MCD Biology, University of California, Santa Cruz, CA, USA.

Department of Bioengineering, Stanford University, Stanford, CA, USA.

出版信息

Synth Biol (Oxf). 2020;5(1):ysaa007. doi: 10.1093/synbio/ysaa007. Epub 2020 Jun 16.

Abstract

Gene expression in 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.

摘要

基因表达在多个层面受到调控。转录因子和染色质因子的基因组和表观基因组图谱绘制,已促成了各种模块化调控元件的描绘——增强子(上游激活序列)、核心启动子、5'非翻译区(5'UTR)以及转录终止子/3'非翻译区(3'UTR)。然而,这些元件中仅有少数与其他元件组合进行过测试,不同模块化调控元件之间的功能相互作用仍有待探索。我们描述了一种构建调控元件组合文库的简单快速方法,并利用该文库研究了26种不同的增强子、核心启动子、5'UTR以及转录终止子/3'UTR,以评估各个调控部分在基因表达中的作用。我们的组合分析表明,虽然增强子启动基因表达,但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正向或负向影响。主成分分析(PCA)表明,增强子和启动子功能可以由单个主成分解释,而UTR功能涉及多个功能成分。PCA还突出了异常值,并暗示了各个元件调控机制的差异。我们的数据还识别出了许多由不同单个调控元件组成的调控盒,它们表现出同等的基因表达水平。因此,这些数据提供了一份元件目录,未来可用于设计合成调控电路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996c/7402160/3b246661b0b3/ysaa007f1.jpg

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