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Bacterial chromatin organization by H-NS protein unravelled using dual DNA manipulation



Both prokaryotic and eukaryotic organisms contain DNA bridging proteins, which can have regulatory or architectural functions1. The molecular and mechanical details of such proteins are hard to obtain, in particular if they involve non-specific interactions. The bacterial nucleoid consists of hundreds of DNA loops, shaped in part by non-specific DNA bridging proteins such as histone-like nucleoid structuring protein (H-NS), leucine-responsive regulatory protein (Lrp) and SMC (structural maintenance of chromosomes) proteins2,3. We have developed an optical tweezers instrument that can independently handle two DNA molecules, which allows the systematic investigation of protein-mediated DNA–DNA interactions. Here we use this technique to investigate the abundant non-specific nucleoid-associated protein H-NS, and show that H-NS is dynamically organized between two DNA molecules in register with their helical pitch. Our optical tweezers also allow us to carry out dynamic force spectroscopy on non-specific DNA binding proteins and thereby to determine an energy landscape for the H-NS–DNA interaction. Our results explain how the bacterial nucleoid can be effectively compacted and organized, but be dynamic in nature and accessible to DNA-tracking motor enzymes. Finally, our experimental approach is widely applicable to other DNA bridging proteins, as well as to complex DNA interactions involving multiple DNA molecules.

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This research was supported by the Netherlands Organization for Scientific Research (NWO) through an NWO-Vernieuwingsimpuls grant (to G.J.L.W.), a FOM-projectruimte grant (to G.J.L.W.), an NWO-VENI grant (to R.T.D.) and a grant from ALW-NWO (to G.J.L.W.). We thank B. van den Broek, N. Goosen, J. van Mameren, E. Peterman, R. Wagner and C. Woldringh for their input and critical reading of the manuscript and J. Kerssemakers for providing the step-fitting algorithm and his assistance using it.

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Reprints and permissions information is available at www.nature.com/reprints. The authors declare no competing financial interests.

Correspondence to Remus T. Dame or Gijs J. L. Wuite.

Supplementary information

  1. Supplementary Methods

    The supplementary methods contains additional methods used in this work (PDF 14 kb)

  2. Supplementary Figures

    This file contains Supplementary Figures 1–4 referred to in the main text (S1, S2, S3 and S4) and Supplementary Notes. (PDF 1019 kb)

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Further reading

Figure 1: Dual DNA manipulation.
Figure 2: Characteristics of H-NS bridges.
Figure 3: Structural models of H-NS and H-NS–DNA 2 complexes.
Figure 4: Kinetics of the H-NS–DNA interaction.


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