Evidence map›Paper›PMID 29766687›Full record

ArticleJournal of biomedical optics2018

Structured illumination to spatially map chromatin motions.

Keith Bonin, Amanda Smelser, Naike Salvador Moreno, George Holzwarth, Kevin Wang, Preston Levy, Pierre-Alexandre Vidi

Open access · goldAbstract read
In one paragraph

Article in Journal of biomedical optics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.3field-weighted citation impact, top 10% of its field
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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. DNA damage reduces heterogeneity and coherence of chromatin motions.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  5. Article
  6. Review
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 at 1 institution in 1 country.

Keith BoninWake Forest University, Department of Physics, Winston-Salem, North Carolina, United States.
Amanda SmelserWake Forest School of Medicine, Department of Cancer Biology, Winston-Salem, North Carolina, United States.
Naike Salvador MorenoWake Forest School of Medicine, Department of Cancer Biology, Winston-Salem, North Carolina, United States.
George HolzwarthWake Forest University, Department of Physics, Winston-Salem, North Carolina, United States.
Kevin WangWake Forest University, Department of Physics, Winston-Salem, North Carolina, United States.
Preston LevyWake Forest University, Department of Physics, Winston-Salem, North Carolina, United States.
Pierre-Alexandre VidiWake Forest School of Medicine, Department of Cancer Biology, Winston-Salem, North Carolina, United States.
Wake Forest University · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
Interplay Between Tissue Architecture and Nuclear Organization in the DNA DamageR00CA163957 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI VIDI, PIERRE-ALEXANDRE · 2015 to 2017
$747k
NCI NIH HHS P30 CA012197NCI NIH HHS R00 CA163957
6 · The paper itself

Abstract

We describe a simple optical method that creates structured illumination of a photoactivatable probe and apply this method to characterize chromatin motions in nuclei of live cells. A laser beam coupled to a diffractive optical element at the back focal plane of an excitation objective generates an array of near diffraction-limited beamlets with FWHM of 340  ±  30  nm, which simultaneously photoactivate a 7  ×  7 matrix pattern of GFP-labeled histones, with spots 1.70  μm apart. From the movements of the photoactivated spots, we map chromatin diffusion coefficients at multiple microdomains of the cell nucleus. The results show correlated motions of nearest chromatin microdomain neighbors, whereas chromatin movements are uncorrelated at the global scale of the nucleus. The method also reveals a DNA damage-dependent decrease in chromatin diffusion. The diffractive optical element instrumentation can be easily and cheaply implemented on commercial inverted fluorescence microscopes to analyze adherent cell culture models. A protocol to measure chromatin motions in nonadherent human hematopoietic stem and progenitor cells is also described. We anticipate that the method will contribute to the identification of the mechanisms regulating chromatin mobility, which influences most genomic processes and may underlie the biogenesis of genomic translocations associated with hematologic malignancies.

Indexed as

Cell Line, TumorCell MovementCell NucleusChromatinEquipment DesignHistonesHumansImage Processing, Computer-AssistedLightingMicroscopy, FluorescenceChromatinHistoneschromatin motiondiffractive opticsdiffusion mapslaser photoactivationparticle trackingstructured illumination

Identifiers

PMID29766687
PMCPMC5987180
OpenAlexW2949149553

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.