Structural diversity of supercoiled DNA

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作者
Rossitza N. Irobalieva
Jonathan M. Fogg
Daniel J. Catanese
Thana Sutthibutpong
Muyuan Chen
Anna K. Barker
Steven J. Ludtke
Sarah A. Harris
Michael F. Schmid
Wah Chiu
Lynn Zechiedrich
机构
[1] Graduate Program in Structural and Computational Biology and Molecular Biophysics,Verna and Marrs McLean Department of Biochemistry and Molecular Biology
[2] Baylor College of Medicine,Department of Molecular Virology and Microbiology
[3] Houston,Department of Pharmacology
[4] Texas 77030 USA,undefined
[5] Baylor College of Medicine,undefined
[6] Houston,undefined
[7] Texas 77030 USA,undefined
[8] Baylor College of Medicine,undefined
[9] Baylor College of Medicine,undefined
[10] School of Physics and Astronomy,undefined
[11] University of Leeds,undefined
来源
Nature Communications | / 6卷
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摘要
By regulating access to the genetic code, DNA supercoiling strongly affects DNA metabolism. Despite its importance, however, much about supercoiled DNA (positively supercoiled DNA, in particular) remains unknown. Here we use electron cryo-tomography together with biochemical analyses to investigate structures of individual purified DNA minicircle topoisomers with defined degrees of supercoiling. Our results reveal that each topoisomer, negative or positive, adopts a unique and surprisingly wide distribution of three-dimensional conformations. Moreover, we uncover striking differences in how the topoisomers handle torsional stress. As negative supercoiling increases, bases are increasingly exposed. Beyond a sharp supercoiling threshold, we also detect exposed bases in positively supercoiled DNA. Molecular dynamics simulations independently confirm the conformational heterogeneity and provide atomistic insight into the flexibility of supercoiled DNA. Our integrated approach reveals the three-dimensional structures of DNA that are essential for its function.
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