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使用Cre-lox技术进行基因组工程的一体化构建体。

All-in-one construct for genome engineering using Cre-lox technology.

作者信息

Mariscal Ana M, González-González Luis, Querol Enrique, Piñol Jaume

机构信息

Departament de Bioquímica i Biologia Molecular and Institut de Biotecnologia i Biomedicina, Universitat Autònoma de Barcelona, Cerdanyola del Vallès 0819, Spain.

Departament de Bioquímica i Biologia Molecular and Institut de Biotecnologia i Biomedicina, Universitat Autònoma de Barcelona, Cerdanyola del Vallès 0819, Spain

出版信息

DNA Res. 2016 Jun;23(3):263-70. doi: 10.1093/dnares/dsw015. Epub 2016 Apr 15.

Abstract

Mycoplasma genitalium is an appealing model of a minimal cell and synthetic biology study, and it was one of the first organisms whose genome was fully sequenced and chemically synthesized. Despite its usefulness as a model organism, many genetic tools well established for other microorganisms are not currently available in mycoplasmas. We have developed several vectors to adapt the Cre-lox technology for genome engineering in M. genitalium, providing an all-in-one construct that could be also useful to obtain unmarked genetic modifications in many other slow growing microorganisms. This construct contains a modified promoter sequence based in TetR system that exhibits an enhanced control on Cre recombinase expression, virtually abolishing the presence of this recombinase in the absence of inducer. This allows to introduce the Cre recombinase gene and the desired genetic modification in a single transformation step. In addition, this inducible promoter may be a very promising tool for a wide range of molecular applications.

摘要

生殖支原体是最小细胞和合成生物学研究的一个有吸引力的模型,它是最早一批基因组被完全测序和化学合成的生物之一。尽管它作为模式生物很有用,但许多为其他微生物建立的成熟遗传工具目前在支原体中还不可用。我们开发了几种载体,以使Cre-lox技术适用于生殖支原体的基因组工程,提供了一种一体化构建体,这对于在许多其他生长缓慢的微生物中获得无标记的基因修饰也可能有用。该构建体包含一个基于TetR系统的修饰启动子序列,对Cre重组酶的表达表现出更强的控制,实际上在没有诱导剂的情况下消除了这种重组酶的存在。这使得在单个转化步骤中就能引入Cre重组酶基因和所需的基因修饰。此外,这种诱导型启动子可能是广泛分子应用中非常有前景的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99e1/4909314/b6baf109e977/dsw01501.jpg

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