Petrushenko Zoya M, Lai Chien-Hung, Rai Rachna, Rybenkov Valentin V
Department of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73019, USA.
J Biol Chem. 2006 Feb 24;281(8):4606-15. doi: 10.1074/jbc.M504754200. Epub 2005 Dec 20.
MukB is a bacterial SMC (structural maintenance of chromosome) protein required for faithful chromosome segregation in Escherichia coli. We report here that purified MukB introduces right-handed knots into DNA in the presence of type-2 topoisomerase, indicating that the protein promotes intramolecular DNA condensation. The pattern of generated knots suggests that MukB, similar to eukaryotic condensins, stabilizes large right-handed DNA loops. In contrast to eukaryotic condensins, however, the net supercoiling stabilized by MukB was negative. Furthermore, DNA reshaping by MukB did not require ATP. These data establish that bacterial condensins alter the shape of double-stranded DNA in vitro and lend support to the notions that the right-handed knotting is the most conserved biochemical property of condensins. Finally, we found that MukB can be eluted from a heparin column in two distinct forms, one of which is inert in DNA binding or reshaping. Furthermore, we find that the activity of MukB is reversibly attenuated during chromatographic separation. Thus, MukB has a unique set of topological properties, compared with other SMC proteins, and is likely to exist in two different conformations.
MukB是一种细菌SMC(染色体结构维持)蛋白,是大肠杆菌中染色体忠实分离所必需的。我们在此报告,纯化的MukB在2型拓扑异构酶存在的情况下会将右手结引入DNA,这表明该蛋白促进分子内DNA凝聚。产生的结的模式表明,MukB与真核凝聚素相似,能稳定大的右手DNA环。然而,与真核凝聚素不同的是,MukB稳定的净超螺旋是负的。此外,MukB介导的DNA重塑不需要ATP。这些数据表明细菌凝聚素在体外会改变双链DNA的形状,并支持右手打结是凝聚素最保守的生化特性这一观点。最后,我们发现MukB可以以两种不同的形式从肝素柱上洗脱下来,其中一种在DNA结合或重塑方面是无活性的。此外,我们发现在色谱分离过程中MukB的活性会可逆地减弱。因此,与其他SMC蛋白相比,MukB具有独特的一组拓扑特性,并且可能以两种不同的构象存在。