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      Reconstituted TAD-size chromatin fibers feature heterogeneous nucleosome clusters

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          Abstract

          Large topologically associated domains (TADs) contain irregularly spaced nucleosome clutches, and interactions between such clutches are thought to aid the compaction of these domains. Here, we reconstituted TAD-sized chromatin fibers containing hundreds of nucleosomes on native source human and lambda-phage DNA and compared their mechanical properties at the single-molecule level with shorter ‘601’ arrays with various nucleosome repeat lengths. Fluorescent imaging showed increased compaction upon saturation of the DNA with histones and increasing magnesium concentration. Nucleosome clusters and their structural fluctuations were visualized in confined nanochannels. Force spectroscopy revealed not only similar mechanical properties of the TAD-sized fibers as shorter fibers but also large rupture events, consistent with breaking the interactions between distant clutches of nucleosomes. Though the arrays of native human DNA, lambda-phage and ‘601’ DNA featured minor differences in reconstitution yield and nucleosome stability, the fibers’ global structural and mechanical properties were similar, including the interactions between nucleosome clutches. These single-molecule experiments quantify the mechanical forces that stabilize large TAD-sized chromatin domains consisting of disordered, dynamically interacting nucleosome clutches and their effect on the condensation of large chromatin domains.

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          For the past twenty five years the NIH family of imaging software, NIH Image and ImageJ have been pioneers as open tools for scientific image analysis. We discuss the origins, challenges and solutions of these two programs, and how their history can serve to advise and inform other software projects.
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            Epigenetics and aging

            Researchers review how random changes and our environment (for example, diet) determines our life span.
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              Determinants of nucleosome organization in primary human cells

              Nucleosomes are the basic packaging units of chromatin, modulating accessibility of regulatory proteins to DNA and thus influencing eukaryotic gene regulation. Elaborate chromatin remodeling mechanisms have evolved that govern nucleosome organization at promoters, regulatory elements, and other functional regions in the genome 1 . Analyses of chromatin landscape have uncovered a variety of mechanisms, including DNA sequence preferences, that can influence nucleosome positions 2–4 . To identify major determinants of nucleosome organization in the human genome, we utilized deep sequencing to map nucleosome positions in three primary human cell types and in vitro. A majority of the genome exhibited substantial flexibility of nucleosome positions while a small fraction showed reproducibly positioned nucleosomes. Certain sites that position in vitro can anchor the formation of nucleosomal arrays that have cell type-specific spacing in vivo. Our results unveil an interplay of sequence-based nucleosome preferences and non-nucleosomal factors in determining nucleosome organization within mammalian cells.
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                Author and article information

                Contributors
                noort@physics.leidenuniv.nl
                larsnor@ntu.edu.sg
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                16 September 2022
                16 September 2022
                2022
                : 12
                : 15558
                Affiliations
                [1 ]GRID grid.59025.3b, ISNI 0000 0001 2224 0361, School of Biological Sciences, , Nanyang Technological University, ; 60 Nanyang Drive, Singapore, 637551 Singapore
                [2 ]GRID grid.27476.30, ISNI 0000 0001 0943 978X, Graduate School of Environmental Studies, , Nagoya University, ; Furo-Cho, Chikusa-Ku, Nagoya, 464-8601 Japan
                [3 ]GRID grid.4280.e, ISNI 0000 0001 2180 6431, Department of Physics, , National University of Singapore, ; Singapore, 117542 Singapore
                [4 ]GRID grid.5132.5, ISNI 0000 0001 2312 1970, Huygens-Kamerlingh Ohnes Laboratory, , Leiden University, ; Niels Bohrweg 2, 2333 CA Leiden, The Netherlands
                [5 ]GRID grid.428397.3, ISNI 0000 0004 0385 0924, Present Address: Department of Emerging Infectious Diseases, , Duke-NUS Medical School, ; Singapore, 169857 Singapore
                Article
                19471
                10.1038/s41598-022-19471-3
                9481575
                36114220
                bf5b17fa-43a0-4d19-b39e-d7e2f6db1f41
                © The Author(s) 2022

                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
                : 28 May 2022
                : 30 August 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001459, Ministry of Education - Singapore;
                Award ID: R-144-000-451-114
                Award ID: 2018-T1-001-114
                Award Recipient :
                Categories
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                © The Author(s) 2022

                Uncategorized
                single-molecule biophysics,biophysics,biochemistry,dna
                Uncategorized
                single-molecule biophysics, biophysics, biochemistry, dna

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