Evidence map›Paper›PMID 33672992›Full record

ArticleInternational journal of molecular sciences2021

Comparing Super-Resolution Microscopy Techniques to Analyze Chromosomes.

Ivona Kubalová, Alžběta Němečková, Klaus Weisshart, Eva Hřibová, Veit Schubert

Open access · goldAbstract readComparative Study
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

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  14. Helical coiling of metaphase chromatids.Nucleic acids research · 2023
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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

5 authors at 3 institutions in 2 countries.

Ivona KubalováLeibniz Institute of Plant Genetics and Crop Plant Research (IPK), Gatersleben, D-06466 Seeland, Germany.ORCID 0000-0002-5673-9715
Alžběta NěmečkováCentre of the Region Hana for Biotechnological and Agricultural Research, Institute of Experimental Botany of the Czech Academy of Sciences, 77900 Olomouc, Czech Republic.ORCID 0000-0002-1926-9443
Klaus WeisshartCarl Zeiss Microscopy GmbH, D-07745 Jena, Germany.
Eva HřibováCentre of the Region Hana for Biotechnological and Agricultural Research, Institute of Experimental Botany of the Czech Academy of Sciences, 77900 Olomouc, Czech Republic.ORCID 0000-0002-6868-4344
Veit SchubertLeibniz Institute of Plant Genetics and Crop Plant Research (IPK), Gatersleben, D-06466 Seeland, Germany.ORCID 0000-0002-3072-0485
Czech Academy of Sciences, Institute of Experimental Botany · CZLeibniz-Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK) · DECarl Zeiss (Germany) · DE

Funding

Deutsche Forschungsgemeinschaft Deutsche Forschungsgemeinschaft (Schu 762/11-1); ERDF project "Plants as a tool for sustainable global development" (grant award CZ.02.1.01/0.0/0.0/16_019/0000827)
6 · The paper itself

Abstract

The importance of fluorescence light microscopy for understanding cellular and sub-cellular structures and functions is undeniable. However, the resolution is limited by light diffraction (~200-250 nm laterally, ~500-700 nm axially). Meanwhile, super-resolution microscopy, such as structured illumination microscopy (SIM), is being applied more and more to overcome this restriction. Instead, super-resolution by stimulated emission depletion (STED) microscopy achieving a resolution of ~50 nm laterally and ~130 nm axially has not yet frequently been applied in plant cell research due to the required specific sample preparation and stable dye staining. Single-molecule localization microscopy (SMLM) including photoactivated localization microscopy (PALM) has not yet been widely used, although this nanoscopic technique allows even the detection of single molecules. In this study, we compared protein imaging within metaphase chromosomes of barley via conventional wide-field and confocal microscopy, and the sub-diffraction methods SIM, STED, and SMLM. The chromosomes were labeled by DAPI (4',6-diamidino-2-phenylindol), a DNA-specific dye, and with antibodies against topoisomerase IIα (Topo II), a protein important for correct chromatin condensation. Compared to the diffraction-limited methods, the combination of the three different super-resolution imaging techniques delivered tremendous additional insights into the plant chromosome architecture through the achieved increased resolution.

Indexed as

Chromosomes, PlantDNA Topoisomerases, Type IIFluorescent DyesHordeumIndolesMetaphaseMicroscopy, ConfocalMicroscopy, FluorescenceReproducibility of ResultsSingle Molecule ImagingDAPIDNA Topoisomerases, Type IIFluorescent DyesIndoleschromatindeconvolution microscopyHordeum vulgaremetaphase chromosomenanoscopyphotoactivated localization microscopystimulated emission depletion microscopystructured illumination microscopytopoisomerase IIwide-field microscopy

Identifiers

PMID33672992
PMCPMC7917581
OpenAlexW3132541761

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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.