Laboratory of Biochemistry and Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892; email:
Chadds Ford, Pennsylvania 19317; email:
Annu Rev Virol. 2015 Nov;2(1):25-40. doi: 10.1146/annurev-virology-100114-054930.
Cre-lox of bacteriophage P1 has become one of the most widely used tools for genetic engineering in eukaryotes. The origins of this tool date to more than 30 years ago when Nat L. Sternberg discovered the recombinase, Cre, and its specific locus of crossover, lox, while studying the maintenance of bacteriophage P1 as a stable plasmid. Recombinations mediated by Cre assist in cyclization of the DNA of infecting phage and in resolution of prophage multimers created by generalized recombination. Early in vitro work demonstrated that, although it shares similarities with the well-characterized bacteriophage λ integration, Cre-lox is in many ways far simpler in its requirements for carrying out recombination. These features would prove critical for its development as a powerful and versatile tool in genetic engineering. We review the history of the discovery and characterization of Cre-lox and touch upon the present direction of Cre-lox research.
Cre-lox 噬菌体 P1 已成为真核生物中基因工程最广泛使用的工具之一。该工具的起源可以追溯到 30 多年前,当时 Nat L. Sternberg 在研究噬菌体 P1 作为稳定质粒的维持时发现了重组酶 Cre 和其特定的交叉位点 lox。Cre 介导的重组有助于感染噬菌体的 DNA 环化,并解决由广义重组产生的噬菌体多聚体的分辨率。早期的体外工作表明,尽管它与经过充分研究的噬菌体 λ 整合具有相似性,但 Cre-lox 在重组执行方面的要求在许多方面要简单得多。这些特性对于将其开发为遗传工程中的强大而通用的工具至关重要。我们回顾了 Cre-lox 的发现和特性的历史,并探讨了 Cre-lox 研究的当前方向。