Stark W M, Grindley N D, Hatfull G F, Boocock M R
Institute of Genetics, University of Glasgow, UK.
EMBO J. 1991 Nov;10(11):3541-8. doi: 10.1002/j.1460-2075.1991.tb04918.x.
The resolvase-catalysed reaction between two res sites in a circular DNA substrate normally gives two circular recombination products linked in a two-noded catenane. Homology between the two res sites at the central overlap dinucleotide of subsite I is important for recombination. Reactions between res sites differing at one position in the central dinucleotide (AC X AT) gave a low yield of recombinants containing mismatched base-pairs, but gave large amounts of a non-recombinant four-noded knot. This result was predicted by a 'simple rotation' model for strand exchange. The mismatch is evidently recognized only after commitment to an initial 180 degrees rotation of the resolvase-linked DNA ends, and it induces a second 180 degrees rotation which restores correct base-pairing at the overlap, giving the four-noded product. Correct base-pairing is not essential for religation, but may be important for release of the products. Characteristic patterns of 4, 6, 8 and 10 node knots, or 4, 8, 12 and 16 node knots were obtained, depending on the reaction conditions and the resolvase. Two pathways for multiple rounds of rotation in 360 degrees steps are inferred. The results support a model for strand exchange by supercoil-directed subunit rotation within a resolvase tetramer.
在环状DNA底物中,两个res位点之间由解离酶催化的反应通常会产生两个以双节点连环体形式相连的环状重组产物。亚位点I中心重叠二核苷酸处的两个res位点之间的同源性对于重组很重要。在中心二核苷酸的一个位置不同(AC×AT)的res位点之间的反应产生了低产量的含有错配碱基对的重组体,但产生了大量的非重组四节点纽结。这一结果由链交换的“简单旋转”模型预测得出。错配显然仅在解离酶连接的DNA末端进行初始180度旋转后才被识别,并且它会诱导第二次180度旋转,从而在重叠处恢复正确的碱基配对,产生四节点产物。正确的碱基配对对于重新连接不是必需的,但可能对产物的释放很重要。根据反应条件和解离酶的不同,会得到4、6、8和10节点纽结或4、8、12和16节点纽结的特征模式。推断出了以360度步长进行多轮旋转的两条途径。这些结果支持了一个通过解离酶四聚体内超螺旋导向的亚基旋转进行链交换的模型。