3.8 Article

Topological diversity of chromatin fibers: Interplay between nucleosome repeat length, DNA linking number and the level of transcription

Journal

AIMS BIOPHYSICS
Volume 2, Issue 4, Pages 613-629

Publisher

AMER INST MATHEMATICAL SCIENCES-AIMS
DOI: 10.3934/biophy.2015.4.613

Keywords

chromatin fiber; nucleosome repeat length; DNA linking number; DNA topology; regulation of transcription

Categories

Funding

  1. Intramural Research Program of the National Institutes of Health (Center for Cancer Research, NCI)
  2. Start-Up Fund of the Rochester Institute of Technology
  3. National Institute of General Medical Sciences [R15GM116102]
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R15GM116102] Funding Source: NIH RePORTER

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The spatial organization of nucleosomes in 30-nm fibers remains unknown in detail. To tackle this problem, we analyzed all stereochemically possible configurations of two-start chromatin fibers with DNA linkers L = 10-70 bp (nucleosome repeat length NRL = 157-217 bp). In our model, the energy of a fiber is a sum of the elastic energy of the linker DNA, steric repulsion, electrostatics, and the H4 tail-acidic patch interaction between two stacked nucleosomes. We found two families of energetically feasible conformations of the fibers-one observed earlier, and the other novel. The fibers from the two families are characterized by different DNA linking numbers-that is, they are topologically different. Remarkably, the optimal geometry of a fiber and its topology depend on the linker length: the fibers with linkers L = 10n and 10n + 5 bp have DNA linking numbers per nucleosome Delta Lk approximate to -1.5 and -1.0, respectively. In other words, the level of DNA supercoiling is directly related to the length of the inter-nucleosome linker in the chromatin fiber (and therefore, to NRL). We hypothesize that this topological polymorphism of chromatin fibers may play a role in the process of transcription, which is known to generate different levels of DNA supercoiling upstream and downstream from RNA polymerase. A genome-wide analysis of the NRL distribution in active and silent yeast genes yielded results consistent with this assumption.

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