Shapiro J A, Leach D
Department of Biochemistry and Molecular Biology, University of Chicago, Illinois 60637.
Genetics. 1990 Oct;126(2):293-9. doi: 10.1093/genetics/126.2.293.
The original Casadaban technique for isolating fused cistrons encoding hybrid beta-galactosidase proteins used a Mucts62 prophage to align the upstream coding sequence and lacZ prior to selection. Kinetic analysis of araB-lacZ fusion colony emergence indicated that the required DNA rearrangements were regulated and responsive to conditions on selection plates. This has been cited as an example of "directed mutation." Here we show genetically that the MuA and integration host factor (IHF) transposition functions are involved in the formation of hybrid araB-lacZ cistrons and propose a molecular model for how fusions can form from the initial strand-transfer complex. These results confirm earlier indications of direct Mu involvement in the fusion process. The proposed model explains how rearranged Mu sequences come to be found as interdomain linkers in certain hybrid cistrons and indicates that the fusion process involves a spatially and temporally coordinated sequence of biochemical reactions.
最初由卡萨达班(Casadaban)提出的用于分离编码杂交β-半乳糖苷酶蛋白的融合顺反子的技术,在选择之前使用Mucts62原噬菌体来使上游编码序列与lacZ对齐。对araB-lacZ融合菌落出现的动力学分析表明,所需的DNA重排受到调控,并且对选择平板上的条件有响应。这被引为“定向突变”的一个例子。在此我们通过遗传学方法表明,MuA和整合宿主因子(IHF)转座功能参与了杂交araB-lacZ顺反子的形成,并提出了一个关于融合如何从初始链转移复合物形成的分子模型。这些结果证实了早期关于Mu直接参与融合过程的迹象。所提出的模型解释了重排的Mu序列如何在某些杂交顺反子中作为结构域间连接子被发现,并表明融合过程涉及一系列在空间和时间上协调的生化反应。