Rothstein R J
Methods Enzymol. 1983;101:202-11. doi: 10.1016/0076-6879(83)01015-0.
The one-step gene disruption techniques described here are versatile in that a disruption can be made simply by the appropriate cloning experiment. The resultant chromosomal insertion is nonreverting and contains a genetically linked marker. Detailed knowledge of the restriction map of a fragment is not necessary. It is even possible to "probe" a fragment that is unmapped for genetic functions by constructing a series of insertions and testing each one for its phenotype.
本文所述的一步基因破坏技术具有通用性,因为仅通过适当的克隆实验就能实现破坏。所产生的染色体插入是不可逆的,并且包含一个基因连锁标记。无需详细了解片段的限制酶切图谱。甚至有可能通过构建一系列插入并测试每个插入的表型,来“探测”一个未绘制基因功能图谱的片段。