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利用Cre/lox系统在小鼠中进行可诱导基因靶向

Inducible gene targeting in mice using the Cre/lox system.

作者信息

Sauer B

机构信息

Laboratory of Biochemistry and Metabolism, National Institute of Diabetes, Digestive and Kidney Disease, Bethesda, Maryland 20892-1800, USA.

出版信息

Methods. 1998 Apr;14(4):381-92. doi: 10.1006/meth.1998.0593.

Abstract

Molecular techniques now allow the design of precise genetic modifications in the mouse. Not only can defined nucleotide changes be engineered into the genome of the mouse, but genetic switches can be designed to target expression or ablation of any gene (for which basic molecular information is available) to any tissue at any defined time. These strategies promise to contribute substantially to an increased understanding of individual gene function in development and pathogenesis. A powerful tool, both for the design of such genetic switches and for speeding the creation of gene-modified animals, is the Cre site-specific DNA recombinase of bacteriophage P1. Precise DNA rearrangements and genetic switches can be efficiently generated in a straightforward manner using Cre recombinase. In conjunction with inducible systems for controlling Cre expression and function, these recombination-based strategies are likely to have a profound impact on developmental biology and the generation of useful animal models of human disease.

摘要

分子技术现在允许在小鼠中设计精确的基因修饰。不仅可以将特定的核苷酸变化引入小鼠基因组,还可以设计基因开关,以便在任何特定时间将任何基因(已有基本分子信息)的表达或缺失靶向到任何组织。这些策略有望极大地促进对个体基因在发育和发病机制中功能的理解。噬菌体P1的Cre位点特异性DNA重组酶是一种强大的工具,可用于设计此类基因开关以及加速基因修饰动物的创建。使用Cre重组酶可以以直接的方式高效地产生精确的DNA重排和基因开关。结合用于控制Cre表达和功能的诱导系统,这些基于重组的策略可能会对发育生物学和人类疾病有用动物模型的产生产生深远影响。

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