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      When 3D genome technology meets viral infection, including SARS‐CoV‐2

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          Abstract

          Mammalian chromosomes undergo varying degrees of compression to form three‐dimensional genome structures. These three‐dimensional structures undergo dynamic and precise chromatin interactions to achieve precise spatial and temporal regulation of gene expression. Most eukaryotic DNA viruses can invade their genomes into the nucleus. However, it is still poorly understood how the viral genome is precisely positioned after entering the host cell nucleus to find the most suitable location and whether it can specifically interact with the host genome to hijack the host transcriptional factories or even integrate into the host genome to complete its transcription and replication rapidly. Chromosome conformation capture technology can reveal long‐range chromatin interactions between different chromosomal sites in the nucleus, potentially providing a reference for viral DNA‐host chromatin interactions. This review summarized the research progress on the three‐dimensional interaction between virus and host genome and the impact of virus integration into the host genome on gene transcription regulation, aiming to provide new insights into chromatin interaction and viral gene transcription regulation, laying the foundation for the treatment of infectious diseases.

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          Most cited references109

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          Is Open Access

          An Integrated Encyclopedia of DNA Elements in the Human Genome

          Summary The human genome encodes the blueprint of life, but the function of the vast majority of its nearly three billion bases is unknown. The Encyclopedia of DNA Elements (ENCODE) project has systematically mapped regions of transcription, transcription factor association, chromatin structure, and histone modification. These data enabled us to assign biochemical functions for 80% of the genome, in particular outside of the well-studied protein-coding regions. Many discovered candidate regulatory elements are physically associated with one another and with expressed genes, providing new insights into the mechanisms of gene regulation. The newly identified elements also show a statistical correspondence to sequence variants linked to human disease, and can thereby guide interpretation of this variation. Overall the project provides new insights into the organization and regulation of our genes and genome, and an expansive resource of functional annotations for biomedical research.
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            A 3D map of the human genome at kilobase resolution reveals principles of chromatin looping.

            We use in situ Hi-C to probe the 3D architecture of genomes, constructing haploid and diploid maps of nine cell types. The densest, in human lymphoblastoid cells, contains 4.9 billion contacts, achieving 1 kb resolution. We find that genomes are partitioned into contact domains (median length, 185 kb), which are associated with distinct patterns of histone marks and segregate into six subcompartments. We identify ∼10,000 loops. These loops frequently link promoters and enhancers, correlate with gene activation, and show conservation across cell types and species. Loop anchors typically occur at domain boundaries and bind CTCF. CTCF sites at loop anchors occur predominantly (>90%) in a convergent orientation, with the asymmetric motifs "facing" one another. The inactive X chromosome splits into two massive domains and contains large loops anchored at CTCF-binding repeats. Copyright © 2014 Elsevier Inc. All rights reserved.
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              Comprehensive mapping of long-range interactions reveals folding principles of the human genome.

              We describe Hi-C, a method that probes the three-dimensional architecture of whole genomes by coupling proximity-based ligation with massively parallel sequencing. We constructed spatial proximity maps of the human genome with Hi-C at a resolution of 1 megabase. These maps confirm the presence of chromosome territories and the spatial proximity of small, gene-rich chromosomes. We identified an additional level of genome organization that is characterized by the spatial segregation of open and closed chromatin to form two genome-wide compartments. At the megabase scale, the chromatin conformation is consistent with a fractal globule, a knot-free, polymer conformation that enables maximally dense packing while preserving the ability to easily fold and unfold any genomic locus. The fractal globule is distinct from the more commonly used globular equilibrium model. Our results demonstrate the power of Hi-C to map the dynamic conformations of whole genomes.
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                Author and article information

                Contributors
                zheng.alan@hotmail.com
                Journal
                J Med Virol
                J Med Virol
                10.1002/(ISSN)1096-9071
                JMV
                Journal of Medical Virology
                John Wiley and Sons Inc. (Hoboken )
                0146-6615
                1096-9071
                10 August 2022
                10 August 2022
                : 10.1002/jmv.28040
                Affiliations
                [ 1 ] Central Laboratory The First Affiliated Hospital of Hebei North University Zhangjiakou China
                [ 2 ] Department of Immunology, School of Basic Medical Sciences Fujian Medical University Fuzhou China
                [ 3 ] Department of Neurology Shenzhen University General Hospital, Shenzhen University Shenzhen, Guangdong Province China
                [ 4 ] Department of Obstetrics and Gynecology Shenzhen University General Hospital Shenzhen, Guangdong China
                [ 5 ] Guangdong Key Laboratory for Biomedical Measurements and Ultrasound Imaging, School of Biomedical Engineering Shenzhen University Health Science Center Shenzhen, Guangdong China
                [ 6 ] Shenzhen Key Laboratory Shenzhen University General Hospital Shenzhen, Guangdong China
                [ 7 ] Department of Mathematics and Computer Science Free University Berlin Berlin Germany
                [ 8 ] Department of Microbiology, Immunology and Infectious Diseases University of Calgary Calgary Alberta Canada
                [ 9 ] The State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, School of Life Sciences Inner Mongolia University Hohhot China
                Author notes
                [*] [* ] Correspondence Chunfu Zheng, Department of Immunology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, China.

                Email: zheng.alan@ 123456hotmail.com

                Author information
                http://orcid.org/0000-0002-8797-1322
                Article
                JMV28040
                10.1002/jmv.28040
                9538846
                35916043
                af978aa4-0ccb-459d-9e2e-327d405ed032
                © 2022 Wiley Periodicals LLC.

                This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

                History
                : 09 July 2022
                : 29 March 2022
                : 30 July 2022
                Page count
                Figures: 3, Tables: 1, Pages: 13, Words: 8638
                Funding
                Funded by: Shenzhen Science and Technology Innovation Program
                Funded by: Shenzhen Key Laboratory Foundation
                Categories
                Review
                Reviews
                Custom metadata
                2.0
                corrected-proof
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.0 mode:remove_FC converted:07.10.2022

                Microbiology & Virology
                3d genome,chromatin interaction,hbv,hi‐c,sars‐cov‐2,viral infection
                Microbiology & Virology
                3d genome, chromatin interaction, hbv, hi‐c, sars‐cov‐2, viral infection

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