Proceedings

EPJ E Highlight - Which sequences make DNA unwrap and breathe?

Nucleosome model with the fully wrapped complex (left) and a partially unwrapped complex.

New study elucidates the DNA sequences that offer the perfect conditions for packaged DNA to unwrap and ‘breathe’, thus allowing genes to be read

Accessing DNA wrapped into basic units of packaging, called nucleosomes, depends on the underlying sequence of DNA building blocks, or base pairs. Like Christmas presents, some nucleosomes are easier to unwrap than others. This is because what makes the double helix stiffer or softer, straight or bent—in other words, what determines its elasticity—is the actual base pair sequence. In a new study published in EPJ E, Jamie Culkin from Leiden University, the Netherlands, and colleagues demonstrate the role of the DNA sequence in making it possible for packaged DNA to open up and let genes be read and expressed.

Back in 1995, the late biochemist Jonathan Widom, from Northwestern University, Illinois, USA, demonstrated that nucleosomes ‘breathe’ for a short time, as the DNA partially unwraps from the protein cylinder. This is due to fluctuations linked to temperature changes. This past experiment measured quite accurately the relative accessibility of different parts of the DNA spool for enzymes that cut that DNA.

Following in his footsteps, the authors developed a model that uses computer simulations and is based on their own previously published coarse grained model of the nucleosome. The previous work posited the existence of a second layer of information in DNA molecules, one that is mechanical in nature. By contrast, in this study, using the nucleosome model with sequence-dependent DNA elasticity, the authors studied the effect of the base pair sequence on the accessibility of the nucleosome for a gene readout. Their approach yields a detailed explanation of how the underlying DNA nanomechanics dictate the physical properties of the nucleosome.

Incidentally, the model could also be used to interpret new studies related to the gene editing technology CRISPR, which is applied to DNA wrapped into nucleosomes, and relies on bacteria acting as an immune system that detects and destroys foreign DNA.

The role of DNA sequences in nucleosome breathing. J. Culkin, L. de Bruin, M. Tompitak, R. Phillips, and H. Schiessel (2017), Eur. Phys. J. E 40: 106, DOI 10.1140/epje/i2017-11596-2

This was our first experience of publishing with EPJ Web of Conferences. We contacted the publisher in the middle of September, just one month prior to the Conference, but everything went through smoothly. We have had published MNPS Proceedings with different publishers in the past, and would like to tell that the EPJ Web of Conferences team was probably the best, very quick, helpful and interactive. Typically, we were getting responses from EPJ Web of Conferences team within less than an hour and have had help at every production stage.
We are very thankful to Solange Guenot, Web of Conferences Publishing Editor, and Isabelle Houlbert, Web of Conferences Production Editor, for their support. These ladies are top-level professionals, who made a great contribution to the success of this issue. We are fully satisfied with the publication of the Conference Proceedings and are looking forward to further cooperation. The publication was very fast, easy and of high quality. My colleagues and I strongly recommend EPJ Web of Conferences to anyone, who is interested in quick high-quality publication of conference proceedings.

On behalf of the Organizing and Program Committees and Editorial Team of MNPS-2019, Dr. Alexey B. Nadykto, Moscow State Technological University “STANKIN”, Moscow, Russia. EPJ Web of Conferences vol. 224 (2019)

ISSN: 2100-014X (Electronic Edition)

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