Sinden R R, Pettijohn D E
Proc Natl Acad Sci U S A. 1981 Jan;78(1):224-8. doi: 10.1073/pnas.78.1.224.
Torsional tension in the DNA double helix can be detected in living cells of Escherichia coli from measurements of the rate of trimethylpsoralen photobinding to the intracellular DNA. Here we show that this tension is relaxed in vivo when single-strand DNA breaks are introduced by gamma-irradiation and that approximately 160 nicks per genome equivalent of DNA are required to relax greater than 95% of the tension. Chromosomes containing less than 160 nicks per genome equivalent lose only a part of the tension, depending on the number of nicks. The remaining tension is maintained during incubations of cells at 0 degrees C. Chromosomes with tension relaxed by incubation of cells with inhibitors of DNA gyrase interact with the trimethylpsoralen probe independently of the number of nicks introduced by gamma-irradiation. The results fit a model in which the chromosome in growing E. coli cells (mean generation time, 30 min) is segregated into 43 +/- 10 domains of supercoiling per genome equivalent of DNA or 120 +/- 30 domains per nucleoid. The number of domains is unchanged in cells depleted of nascent RNA by growth with rifampicin, but varies somewhat in cells growing at different rates in different media.
通过测量三甲基补骨脂素与细胞内DNA的光结合速率,可以在大肠杆菌的活细胞中检测到DNA双螺旋中的扭转张力。我们在此表明,当通过γ射线照射引入单链DNA断裂时,这种张力在体内会得到缓解,并且每基因组当量的DNA大约需要160个切口才能缓解超过95%的张力。每基因组当量含有少于160个切口的染色体仅会缓解部分张力,这取决于切口的数量。在0℃下培养细胞期间,剩余的张力会保持。通过用DNA促旋酶抑制剂培养细胞而使张力得到缓解的染色体,与三甲基补骨脂素探针的相互作用与γ射线照射引入的切口数量无关。这些结果符合一个模型,即生长中的大肠杆菌细胞(平均世代时间为30分钟)中的染色体被分离成每基因组当量的DNA有43±10个超螺旋结构域,或每个类核有120±30个结构域。在用利福平生长而耗尽新生RNA的细胞中,结构域的数量没有变化,但在不同培养基中以不同速率生长的细胞中,结构域的数量会有所不同。