Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Published:

Probing SWI/SNF remodeling of the nucleosome by unzipping single DNA molecules

Abstract

Chromatin-remodeling enzymes can overcome strong histone-DNA interactions within the nucleosome to regulate access of DNA-binding factors to the genetic code. By unzipping individual DNA duplexes, each containing a uniquely positioned nucleosome flanked by long segments of DNA, we directly probed histone-DNA interactions. The resulting disruption-force signatures were characteristic of the types and locations of interactions and allowed measurement of the positions of nucleosomes with 2.6-base-pair (bp) precision. Nucleosomes remodeled by yeast SWI/SNF were moved bidirectionally along the DNA, resulting in a continuous position distribution. The characteristic distance of motion was 28 bp per remodeling event, and each event occurred with a catalytic efficiency of 0.4 min−1 per nM SWI/SNF. Remodeled nucleosomes had essentially identical disruption signatures to those of unremodeled nucleosomes, indicating that their overall structure remained canonical. These results impose substantial constraints on the mechanism of SWI/SNF remodeling.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Experimental setup and raw data.
Figure 2: Unzipping through unremodeled and remodeled nucleosomes.
Figure 3: Kinetics of SWI/SNF-catalyzed nucleosome remodeling.

Similar content being viewed by others

References

  1. Davey, C.A., Sargent, D.F., Luger, K., Maeder, A.W. & Richmond, T.J. Solvent mediated interactions in the structure of the nucleosome core particle at 1.9 Å resolution. J. Mol. Biol. 319, 1097–1113 (2002).

    Article  CAS  Google Scholar 

  2. Kingston, R.E. & Narlikar, G.J. ATP-dependent remodeling and acetylation as regulators of chromatin fluidity. Genes Dev. 13, 2339–2352 (1999).

    Article  CAS  Google Scholar 

  3. Kornberg, R.D. & Lorch, Y. Twenty-five years of the nucleosome, fundamental particle of the eukaryote chromosome. Cell 98, 285–294 (1999).

    Article  CAS  Google Scholar 

  4. Vignali, M., Hassan, A.H., Neely, K.E. & Workman, J.L. ATP-dependent chromatin-remodeling complexes. Mol. Cell. Biol. 20, 1899–1910 (2000).

    Article  CAS  Google Scholar 

  5. Smith, C.L. & Peterson, C.L. ATP-dependent chromatin remodeling. Curr. Top. Dev. Biol. 65, 115–148 (2005).

    Article  CAS  Google Scholar 

  6. Becker, P.B. & Horz, W. ATP-dependent nucleosome remodeling. Annu. Rev. Biochem. 71, 247–273 (2002).

    Article  CAS  Google Scholar 

  7. Winston, F. & Carlson, M. Yeast SNF/SWI transcriptional activators and the SPT/SIN chromatin connection. Trends Genet. 8, 387–391 (1992).

    Article  CAS  Google Scholar 

  8. Sudarsanam, P. & Winston, F. The Swi/Snf family nucleosome-remodeling complexes and transcriptional control. Trends Genet. 16, 345–351 (2000).

    Article  CAS  Google Scholar 

  9. Bazett-Jones, D.P., Cote, J., Landel, C.C., Peterson, C.L. & Workman, J.L. The SWI/SNF complex creates loop domains in DNA and polynucleosome arrays and can disrupt DNA-histone contacts within these domains. Mol. Cell. Biol. 19, 1470–1478 (1999).

    Article  CAS  Google Scholar 

  10. Schnitzler, G.R. et al. Direct imaging of human SWI/SNF-remodeled mono- and polynucleosomes by atomic force microscopy employing carbon nanotube tips. Mol. Cell. Biol. 21, 8504–8511 (2001).

    Article  CAS  Google Scholar 

  11. Aoyagi, S. et al. Nucleosome remodeling by the human SWI/SNF complex requires transient global disruption of histone-DNA interactions. Mol. Cell. Biol. 22, 3653–3662 (2002).

    Article  CAS  Google Scholar 

  12. Narlikar, G.J., Phelan, M.L. & Kingston, R.E. Generation and interconversion of multiple distinct nucleosomal states as a mechanism for catalyzing chromatin fluidity. Mol. Cell 8, 1219–1230 (2001).

    Article  CAS  Google Scholar 

  13. Kassabov, S.R., Zhang, B., Persinger, J. & Bartholomew, B. SWI/SNF unwraps, slides, and rewraps the nucleosome. Mol. Cell 11, 391–403 (2003).

    Article  CAS  Google Scholar 

  14. Fan, H.Y., He, X., Kingston, R.E. & Narlikar, G.J. Distinct strategies to make nucleosomal DNA accessible. Mol. Cell 11, 1311–1322 (2003).

    Article  CAS  Google Scholar 

  15. Cote, J., Peterson, C.L. & Workman, J.L. Perturbation of nucleosome core structure by the SWI/SNF complex persists after its detachment, enhancing subsequent transcription factor binding. Proc. Natl. Acad. Sci. USA 95, 4947–4952 (1998).

    Article  CAS  Google Scholar 

  16. Schnitzler, G., Sif, S. & Kingston, R.E. Human SWI/SNF interconverts a nucleosome between its base state and a stable remodeled state. Cell 94, 17–27 (1998).

    Article  CAS  Google Scholar 

  17. Lorch, Y., Cairns, B.R., Zhang, M. & Kornberg, R.D. Activated RSC-nucleosome complex and persistently altered form of the nucleosome. Cell 94, 29–34 (1998).

    Article  CAS  Google Scholar 

  18. Jaskelioff, M., Gavin, I.M., Peterson, C.L. & Logie, C. SWI-SNF-mediated nucleosome remodeling: role of histone octamer mobility in the persistence of the remodeled state. Mol. Cell. Biol. 20, 3058–3068 (2000).

    Article  CAS  Google Scholar 

  19. Flaus, A. & Owen-Hughes, T. Dynamic properties of nucleosomes during thermal and ATP-driven mobilization. Mol. Cell. Biol. 23, 7767–7779 (2003).

    Article  CAS  Google Scholar 

  20. Zofall, M., Persinger, J., Kassabov, S.R. & Bartholomew, B. Chromatin remodeling by ISW2 and SWI/SNF requires DNA translocation inside the nucleosome. Nat. Struct. Mol. Biol. 13, 339–346 (2006).

    Article  CAS  Google Scholar 

  21. Whitehouse, I. et al. Nucleosome mobilization catalysed by the yeast SWI/SNF complex. Nature 400, 784–787 (1999).

    Article  CAS  Google Scholar 

  22. Koch, S.J., Shundrovsky, A., Jantzen, B.C. & Wang, M.D. Probing protein-DNA interactions by unzipping a single DNA double helix. Biophys. J. 83, 1098–1105 (2002).

    Article  CAS  Google Scholar 

  23. Koch, S.J. & Wang, M.D. Dynamic force spectroscopy of protein-DNA interactions by unzipping DNA. Phys. Rev. Lett. 91, 028103 (2003).

    Article  Google Scholar 

  24. Jiang, J. et al. Detection of high-affinity and sliding clamp modes for MSH2–MSH6 by single-molecule unzipping force analysis. Mol. Cell 20, 771–781 (2005).

    Article  CAS  Google Scholar 

  25. Lowary, P.T. & Widom, J. New DNA sequence rules for high affinity binding to histone octamer and sequence-directed nucleosome positioning. J. Mol. Biol. 276, 19–42 (1998).

    Article  CAS  Google Scholar 

  26. Thastrom, A., Bingham, L.M. & Widom, J. Nucleosomal locations of dominant DNA sequence motifs for histone-DNA interactions and nucleosome positioning. J. Mol. Biol. 338, 695–709 (2004).

    Article  CAS  Google Scholar 

  27. Luger, K., Mader, A.W., Richmond, R.K., Sargent, D.F. & Richmond, T.J. Crystal structure of the nucleosome core particle at 2.8 Å resolution. Nature 389, 251–260 (1997).

    Article  CAS  Google Scholar 

  28. Brower-Toland, B.D. et al. Mechanical disruption of individual nucleosomes reveals a reversible multistage release of DNA. Proc. Natl. Acad. Sci. USA 99, 1960–1965 (2002).

    Article  CAS  Google Scholar 

  29. Brower-Toland, B. & Wang, M.D. Use of optical trapping techniques to study single-nucleosome dynamics. Methods Enzymol. 376, 62–72 (2004).

    Article  CAS  Google Scholar 

  30. Brower-Toland, B. et al. Specific contributions of histone tails and their acetylation to the mechanical stability of nucleosomes. J. Mol. Biol. 346, 135–146 (2005).

    Article  CAS  Google Scholar 

  31. Meersseman, G., Pennings, S. & Bradbury, E.M. Mobile nucleosomes—a general behavior. EMBO J. 11, 2951–2959 (1992).

    Article  CAS  Google Scholar 

  32. Cote, J., Quinn, J., Workman, J.L. & Peterson, C.L. Stimulation of GAL4 derivative binding to nucleosomal DNA by the yeast SWI/SNF complex. Science 265, 53–60 (1994).

    Article  CAS  Google Scholar 

  33. Bruno, M. et al. Histone H2A/H2B dimer exchange by ATP-dependent chromatin remodeling activities. Mol. Cell 12, 1599–1606 (2003).

    Article  CAS  Google Scholar 

  34. Vicent, G.P. et al. DNA instructed displacement of histones H2A and H2B at an inducible promoter. Mol. Cell 16, 439–452 (2004).

    Article  CAS  Google Scholar 

  35. Schafer, D.A., Gelles, J., Sheetz, M.P. & Landick, R. Transcription by single molecules of RNA polymerase observed by light microscopy. Nature 352, 444–448 (1991).

    Article  CAS  Google Scholar 

  36. Lee, K.-M. & Narlikar, G. Assembly of nucleosomal templates by salt dialysis. in Current Protocols in Molecular Biology Vol. 3 (eds. Ausubel, F.A. et al.) 21.6.3 (Wiley, New York, 2001).

    Google Scholar 

  37. Smith, C.L., Horowitz-Scherer, R., Flanagan, J.F., Woodcock, C.L. & Peterson, C.L. Structural analysis of the yeast SWI/SNF chromatin remodeling complex. Nat. Struct. Biol. 10, 141–145 (2003).

    Article  CAS  Google Scholar 

  38. Bockelmann, U., Essevaz-Roulet, B. & Heslot, F. DNA strand separation studied by single molecule force measurements. Phys. Rev. E 58, 2386–2394 (1998).

    Article  CAS  Google Scholar 

  39. Orear, J. Notes on statistics for physicists. (Laboratory for Nuclear Studies report CLNS 82/511, Cornell University, New York, 1982).

Download references

Acknowledgements

We thank M. Hall for help with data analysis, L. Bai, J. Jin, B. Brower-Toland, R.M. Fulbright, D. Wacker, J. Tang, V. Elser and J.P. Sethna for helpful suggestions, members of the Wang laboratory for critical comments on the manuscript, J. Widom (Northwestern University) and R. Landick (University of Wisconsin) for gifts of plasmids and the National Cell Culture Center for HeLa cells. This research was supported by US National Institutes of Health grants to J.T.L, C.L.P. and M.D.W and the Keck Foundation's Distinguished Young Scholar Award to M.D.W.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Michelle D Wang.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Supplementary Fig. 1

Cross-correlation position alignment (PDF 80 kb)

Supplementary Fig. 2

Examples of individual traces of disruption force vs. number of base pairs unzipped (PDF 56 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Shundrovsky, A., Smith, C., Lis, J. et al. Probing SWI/SNF remodeling of the nucleosome by unzipping single DNA molecules. Nat Struct Mol Biol 13, 549–554 (2006). https://doi.org/10.1038/nsmb1102

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nsmb1102

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing