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The bacterial condensin MukB compacts DNA by sequestering supercoils and stabilizing topologically isolated loops

机译:细菌凝缩蛋白MukB通过隔离超螺旋并稳定拓扑分离的环来压缩DNA

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摘要

MukB is a structural maintenance of chromosome-like protein required for DNA condensation. The complete condensin is a large tripartite complex of MukB, the kleisin, MukF, and an accessory protein, MukE. As found previously, MukB DNA condensation is a stepwise process. We have defined these steps topologically. They proceed first via the formation of negative supercoils that are sequestered by the protein followed by hinge–hinge interactions between MukB dimers that stabilize topologically isolated loops in the DNA. MukB itself is sufficient to mediate both of these topological alterations; neither ATP nor MukEF is required. We show that the MukB hinge region binds DNA and that this region of the protein is involved in sequestration of supercoils. Cells carrying mutations in the MukB hinge that reduce DNA condensation in vitro exhibit nucleoid decondensation in vivo.
机译:MukB是DNA浓缩所需的染色体样蛋白的结构维持。完整的凝集素是MukB,kleisin,MukF和辅助蛋白MukE的大型三方复合物。如前所述,MukB DNA缩合是一个逐步过程。我们已经按照拓扑定义了这些步骤。它们首先通过被蛋白质螯合的负超螺旋形成,然后是MukB二聚体之间的铰链-铰链相互作用,从而稳定了DNA中拓扑分离的环。 MukB本身足以介导这两种拓扑更改;不需要ATP和MukEF。我们表明,MukB铰链区结合DNA,并且该蛋白质的这一区域参与了超螺旋的螯合。在MukB铰链中携带突变的细胞可在体外减少DNA缩合,在体内显示出类核苷的缩聚。

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