| Literature DB >> 29052214 |
Sophie Desset1, Axel Poulet1,2, Christophe Tatout3.
Abstract
Image analysis is a classical way to study nuclear organization. While nuclear organization used to be investigated by colorimetric or fluorescent labeling of DNA or specific nuclear compartments, new methods in microscopy imaging now enable qualitative and quantitative analyses of chromatin pattern, and nuclear size and shape. Several procedures have been developed to prepare samples in order to collect 3D images for the analysis of spatial chromatin organization, but only few preserve the positional information of the cell within its tissue context. Here, we describe a whole mount tissue preparation procedure coupled to DNA staining using the PicoGreen® intercalating agent suitable for image analysis of the nucleus in living and fixed tissues. 3D Image analysis is then performed using NucleusJ, an open source ImageJ plugin, which allows for quantifying variations in nuclear morphology such as nuclear volume, sphericity, elongation, and flatness as well as in heterochromatin content and position in respect to the nuclear periphery.Entities:
Keywords: 3D nuclear morphology; Chromocenters; Heterochromatin; ImageJ; Nucleus; NucleusJ
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Year: 2018 PMID: 29052214 DOI: 10.1007/978-1-4939-7318-7_33
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745