Yigit H, Reznikoff W S
Department of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
J Bacteriol. 1998 Nov;180(22):5866-74. doi: 10.1128/JB.180.22.5866-5874.1998.
Tn5 transposase (Tnp) overproduction is lethal to Escherichia coli. The overproduction causes cell filamentation and abnormal chromosome segregation. Here we present three lines of evidence strongly suggesting that Tnp overproduction killing is due to titration of topoisomerase I. First, a suppressor mutation of transposase overproduction killing, stkD10, is localized in topA (the gene for topoisomerase I). The stkD10 mutant has the following characteristics: first, it has an increased abundance of topoisomerase I protein, the topoisomerase I is defective for the DNA relaxation activity, and DNA gyrase activity is reduced; second, the suppressor phenotype of a second mutation localized in rpoH, stkA14 (H. Yigit and W. S. Reznikoff, J. Bacteriol. 179:1704-1713, 1997), can be explained by an increase in topA expression; and third, overexpression of wild-type topA partially suppresses the killing. Finally, topoisomerase I was found to enhance Tn5 transposition up to 30-fold in vivo.
Tn5转座酶(Tnp)过量表达对大肠杆菌是致死性的。这种过量表达会导致细胞丝化和异常的染色体分离。在此,我们提供三条证据,有力地表明Tnp过量表达导致的杀伤作用是由于拓扑异构酶I的滴定效应。首先,转座酶过量表达致死的一个抑制突变体stkD10定位于topA(拓扑异构酶I的基因)。stkD10突变体具有以下特征:第一,它具有增加的拓扑异构酶I蛋白丰度,该拓扑异构酶I的DNA松弛活性有缺陷,并且DNA促旋酶活性降低;第二,位于rpoH的第二个突变体stkA14的抑制表型(H. Yigit和W. S. Reznikoff,《细菌学杂志》179:1704 - 1713,1997),可以通过topA表达的增加来解释;第三,野生型topA的过表达部分抑制了杀伤作用。最后,发现拓扑异构酶I在体内可将Tn5转座增强多达30倍。