植物转录抑制工具包的设计和特征描述

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS ACS Synthetic Biology Pub Date : 2024-10-18 Epub Date: 2024-09-23 DOI:10.1021/acssynbio.4c00404
Kasey Markel, Jean Sabety, Shehan Wijesinghe, Patrick M Shih
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引用次数: 0

摘要

基因表达调控对所有生命都至关重要。因此,操纵基因表达水平的工具在生物系统工程中被证明是非常有价值的。然而,在植物中减少基因表达的基因部分(通常称为转录抑制因子)很少有表征清楚的。我们从已知最大的抑制因子家族中挑选了约 25% 的成员,建立了一个包含抑制基团的文库,对其抑制活性进行了鉴定。结合序列信息和反式调控功能数据,我们接下来生成了一个事先预测了功能的合成转录抑制基调库。在对我们的合成库进行表征后,我们不仅证明了我们的许多合成构建物具有抑制因子的功能,还证明了我们对抑制强度的提前预测优于随机猜测。最后,我们评估了来自多种真核生物的已知转录抑制基团的功能。我们的研究代表了迄今为止实验表征的最大的植物抑制基团库,为调整植物转录提供了独特的机会。
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Design and Characterization of a Transcriptional Repression Toolkit for Plants.

Regulation of gene expression is essential for all life. Tools to manipulate the gene expression level have therefore proven to be very valuable in efforts to engineer biological systems. However, there are few well-characterized genetic parts that reduce gene expression in plants, commonly known as transcriptional repressors. We characterized the repression activity of a library consisting of repression motifs from approximately 25% of the members of the largest known family of repressors. Combining sequence information with our trans-regulatory function data, we next generated a library of synthetic transcriptional repression motifs with function predicted in advance. After characterizing our synthetic library, we demonstrated not only that many of our synthetic constructs were functional as repressors but also that our advance predictions of repression strength were better than random guesses. Finally, we assessed the functionality of known transcriptional repression motifs from a wide range of eukaryotes. Our study represents the largest plant repressor motif library experimentally characterized to date, providing unique opportunities for tuning transcription in plants.

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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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