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通过控制质粒拷贝数实现核糖开关信号放大

Riboswitch Signal Amplification by Controlling Plasmid Copy Number.

作者信息

Dwidar Mohammed, Yokobayashi Yohei

机构信息

Nucleic Acid Chemistry and Engineering Unit , Okinawa Institute of Science and Technology Graduate University , Onna , Okinawa 904 0495 , Japan.

出版信息

ACS Synth Biol. 2019 Feb 15;8(2):245-250. doi: 10.1021/acssynbio.8b00454. Epub 2019 Feb 1.

Abstract

Riboswitches are cis-acting RNA devices in mRNAs that control gene expression in response to chemical inputs. As RNA aptamers that recognize diverse classes of molecules can be isolated by in vitro selection, synthetic riboswitches hold promise for various applications in synthetic biology. One of the major drawbacks of riboswitches, however, is their limited dynamic range. A high level of gene expression in the OFF state (leakage) is also a common problem. To address these challenges, we designed and constructed a dual-riboswitch plasmid in which two genes are controlled by theophylline-activated riboswitches. One riboswitch controls the gene of interest, and another riboswitch controls RepL, a phage-derived replication protein that regulates the plasmid copy number. This single-plasmid system afforded an ON/OFF ratio as high as 3900. Furthermore, we used the system to control CRISPR interference (CRISPRi) targeting endogenous genes, and successfully observed expected phenotypic changes in Escherichia coli.

摘要

核糖开关是mRNA中的顺式作用RNA元件,可根据化学输入控制基因表达。由于可以通过体外筛选分离出识别多种分子类别的RNA适体,合成核糖开关在合成生物学的各种应用中具有广阔前景。然而,核糖开关的一个主要缺点是其动态范围有限。在关闭状态下高水平的基因表达(渗漏)也是一个常见问题。为应对这些挑战,我们设计并构建了一种双核糖开关质粒,其中两个基因由茶碱激活的核糖开关控制。一个核糖开关控制目标基因,另一个核糖开关控制RepL,一种调节质粒拷贝数的噬菌体衍生复制蛋白。这个单质粒系统的开/关比高达3900。此外,我们使用该系统控制靶向内源基因的CRISPR干扰(CRISPRi),并在大肠杆菌中成功观察到预期的表型变化。

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