West S C, Cassuto E, Howard-Flanders P
Mol Gen Genet. 1982;187(2):209-17. doi: 10.1007/BF00331119.
We have used a sensitive gel electrophoresis assay to detect the products of Escherichia coli RecA protein catalysed strand exchange reactions between gapped and duplex DNA molecules. We identify structures that correspond to joint molecules formed by homologous pairing, and show that joint molecules are converted by RecA protein into heteroduplex monomers by reciprocal strand exchanges. However, strand exchanges only occur when there is a 3'-terminus complementary to the single stranded DNA in the gap. In the absence of a complementary free end, the two DNA molecules pair and short heteroduplex regions are formed by localised interwinding.
我们使用了一种灵敏的凝胶电泳分析方法来检测大肠杆菌RecA蛋白催化的带缺口DNA分子与双链DNA分子之间的链交换反应产物。我们鉴定出了与同源配对形成的连接分子相对应的结构,并表明连接分子通过RecA蛋白通过相互链交换转化为异源双链单体。然而,链交换仅在缺口处存在与单链DNA互补的3'-末端时才会发生。在没有互补游离末端的情况下,两个DNA分子配对并通过局部缠绕形成短的异源双链区域。