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      Prospects and limitations of expansion microscopy in chromatin ultrastructure determination

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          Abstract

          Expansion microscopy (ExM) is a method to magnify physically a specimen with preserved ultrastructure. It has the potential to explore structural features beyond the diffraction limit of light. The procedure has been successfully used for different animal species, from isolated macromolecular complexes through cells to tissue slices. Expansion of plant-derived samples is still at the beginning, and little is known, whether the chromatin ultrastructure becomes altered by physical expansion. In this study, we expanded isolated barley nuclei and compared whether ExM can provide a structural view of chromatin comparable with super-resolution microscopy. Different fixation and denaturation/digestion conditions were tested to maintain the chromatin ultrastructure. We achieved up to ~4.2-times physically expanded nuclei corresponding to a maximal resolution of ~50–60 nm when imaged by wild-field (WF) microscopy. By applying structured illumination microscopy (SIM, super-resolution) doubling the WF resolution, the chromatin structures were observed at a resolution of ~25–35 nm. WF microscopy showed a preserved nucleus shape and nucleoli. Moreover, we were able to detect chromatin domains, invisible in unexpanded nuclei. However, by applying SIM, we observed that the preservation of the chromatin ultrastructure after the expansion was not complete and that the majority of the tested conditions failed to keep the ultrastructure. Nevertheless, using expanded nuclei, we localized successfully centromere repeats by fluorescence in situ hybridization (FISH) and the centromere-specific histone H3 variant CENH3 by indirect immunolabelling. However, although these repeats and proteins were localized at the correct position within the nuclei (indicating a Rabl orientation), their ultrastructural arrangement was impaired.

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          The online version of this article (10.1007/s10577-020-09637-y) contains supplementary material, which is available to authorized users.

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          Optical imaging. Expansion microscopy.

          In optical microscopy, fine structural details are resolved by using refraction to magnify images of a specimen. We discovered that by synthesizing a swellable polymer network within a specimen, it can be physically expanded, resulting in physical magnification. By covalently anchoring specific labels located within the specimen directly to the polymer network, labels spaced closer than the optical diffraction limit can be isotropically separated and optically resolved, a process we call expansion microscopy (ExM). Thus, this process can be used to perform scalable superresolution microscopy with diffraction-limited microscopes. We demonstrate ExM with apparent ~70-nanometer lateral resolution in both cultured cells and brain tissue, performing three-color superresolution imaging of ~10(7) cubic micrometers of the mouse hippocampus with a conventional confocal microscope.
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            Estimation of nuclear DNA content in plants using flow cytometry.

            Flow cytometry (FCM) using DNA-selective fluorochromes is now the prevailing method for the measurement of nuclear DNA content in plants. Ease of sample preparation and high sample throughput make it generally better suited than other methods such as Feulgen densitometry to estimate genome size, level of generative polyploidy, nuclear replication state and endopolyploidy (polysomaty). Here we present four protocols for sample preparation (suspensions of intact cell nuclei) and describe the analysis of nuclear DNA amounts using FCM. We consider the chemicals and equipment necessary, the measurement process, data analysis, and describe the most frequent problems encountered with plant material such as the interference of secondary metabolites. The purpose and requirement of internal and external standardization are discussed. The importance of using a correct terminology for DNA amounts and genome size is underlined, and its basic principles are explained.
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              Imaging cellular ultrastructures using expansion microscopy (U-ExM)

              The attribution of a protein to an ultrastructural element by optical microscopy represents a major challenge in biology. Here, we report a method of near-native expansion microscopy (U-ExM), enabling the visualization of preserved ultrastructures of macromolecules by optical microscopy. Combined with super-resolution, U-ExM unveiled the centriolar chirality, only visualizable by electron microscopy. We demonstrate the general applicability of U-ExM by imaging different cellular structures including microtubules and mitochondria in cellulo.
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                Author and article information

                Contributors
                schubertv@ipk-gatersleben.de
                Journal
                Chromosome Res
                Chromosome Res
                Chromosome Research
                Springer Netherlands (Dordrecht )
                0967-3849
                1573-6849
                17 September 2020
                17 September 2020
                2020
                : 28
                : 3
                : 355-368
                Affiliations
                [1 ]GRID grid.418934.3, ISNI 0000 0001 0943 9907, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, ; 06466 Seeland, Germany
                [2 ]GRID grid.418095.1, ISNI 0000 0001 1015 3316, Laboratory of Adaptive Immunity, Institute of Molecular Genetics,, , Academy of Sciences of the Czech Republic, ; Prague, Czech Republic
                [3 ]GRID grid.424549.a, ISNI 0000 0004 0379 7801, Carl Zeiss Microscopy GmbH, ; 07745 Jena, Germany
                Author notes

                Responsible Editor: Jiming Jiang

                Author information
                http://orcid.org/0000-0002-3072-0485
                Article
                9637
                10.1007/s10577-020-09637-y
                7691311
                32939606
                5fba36b2-9bb7-4325-9fca-e80142bd661b
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 1 June 2020
                : 28 July 2020
                : 5 August 2020
                Funding
                Funded by: Deutsche Forschungsgemeinschaft
                Award ID: Schu 762/11-1
                Award Recipient :
                Funded by: Czech Science Foundation
                Award ID: 17-20613Y
                Award Recipient :
                Categories
                Original Article
                Custom metadata
                © Springer Nature B.V. 2020

                Genetics
                chromatin,expansion microscopy,nucleus,structured illumination microscopy,hordeum vulgare
                Genetics
                chromatin, expansion microscopy, nucleus, structured illumination microscopy, hordeum vulgare

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