Evidence map›Paper›PMID 31732143›Full record

ArticleBiophysical journal2019

Quantitative Modeling of Nucleosome Unwrapping from Both Ends.

Dengke Zhao, Jenny V Le, Michael A Darcy, Kyle Crocker, Michael G Poirier, Carlos Castro, Ralf Bundschuh

Abstract read
In one paragraph

Article in Biophysical journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Dengke ZhaoInterdisciplinary Biophysics Graduate Program, The Ohio State University, Columbus, Ohio.
Jenny V LeInterdisciplinary Biophysics Graduate Program, The Ohio State University, Columbus, Ohio.
Michael A DarcyDepartment of Physics, The Ohio State University, Columbus, Ohio.
Kyle CrockerDepartment of Physics, The Ohio State University, Columbus, Ohio.
Michael G PoirierInterdisciplinary Biophysics Graduate Program, The Ohio State University, Columbus, Ohio; Department of Physics, The Ohio State University, Columbus, Ohio; Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio.
Carlos CastroInterdisciplinary Biophysics Graduate Program, The Ohio State University, Columbus, Ohio; Department of Mechanical and Aerospace Engineering, The Ohio State University, Columbus, Ohio.
Ralf BundschuhInterdisciplinary Biophysics Graduate Program, The Ohio State University, Columbus, Ohio; Department of Physics, The Ohio State University, Columbus, Ohio; Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio; Division of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, Ohio; Center for RNA Biology, The Ohio State University, Columbus, Ohio. Electronic address: bundschuh@mps.ohio-state.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In eukaryotic cells, DNA is packaged into chromatin where nucleosomes are the basic packaging unit. Important cellular processes including gene expression, DNA replication, and DNA repair require nucleosomal DNA to be unwrapped so that functional proteins can access their target sites, which otherwise are sterically occluded. A key question in this process is what the unwrapped conformations individual nucleosomes adopt within chromatin are. Here, we develop a concurrent nucleosome unwrapping model to address this question. We hypothesize that for a given end-to-end distance of the nucleosomal DNA, the nucleosomal DNA stochastically unwraps from the histone core from both ends independently and that this combination of unwrapping from both sides results in a significant increase in the average distance between the DNA extending from both sides of the nucleosomes. We test our model on recently published experiments using a DNA origami nanocaliper that quantifies nucleosome unwrapping and achieve good agreement between experiment and model prediction. We then investigate the DNA origami caliper distribution when attached to a hexasome (a nucleosome lacking an H2A/H2B dimer). A significant shift in the caliper angle distribution caused by the asymmetric structural features of the hexasome seen experimentally is consistent with the model. Our modeling approach may be more broadly useful to the interpretation of other studies of nucleosome dynamics, chromatin dynamics, and regulatory processes involving nucleosome unwrapping, as well as more generally to optimization of future DNA origami designs to probe mechanical properties of biomolecules.

Indexed as

Models, MolecularBase SequenceDNANanostructuresNucleosomesThermodynamicsDNANucleosomes

Identifiers

PMID31732143
PMCPMC6895690

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.