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Nature communications. 2019 Mar 29;10(1):1408. doi: 10.1038/s41467-019-09391-8 Q115.72025

Structure mapping of dengue and Zika viruses reveals functional long-range interactions

登革病毒和寨卡病毒的结构映射揭示了功能性的长程相互作用 翻译改进

Roland G Huber  1, Xin Ni Lim  2, Wy Ching Ng  3, Adelene Y L Sim  1, Hui Xian Poh  2, Yang Shen  4, Su Ying Lim  2, Karin B Sundstrom  3, Xuyang Sun  5  6, Jong Ghut Aw  2, Horng Khit Too  7  8, Peng Hee Boey  7  8, Andreas Wilm  4, Tanu Chawla  3, Milly M Choy  9  10, Lu Jiang  11  12, Paola Florez de Sessions  13, Xian Jun Loh  11  12, Sylvie Alonso  7  8, Martin Hibberd  9  10, Niranjan Nagarajan  4, Eng Eong Ooi  3  7  14, Peter J Bond  15, October M Sessions  16  17  18, Yue Wan  19  20  21

作者单位 +展开

作者单位

  • 1 Bioinformatics Institute (A*STAR), 30 Biopolis Street #07-01, Matrix, Singapore, 138671, Singapore.
  • 2 Stem Cell and Regenerative Biology, Genome Institute of Singapore, Singapore, 138672, Singapore.
  • 3 Program in Emerging Infectious Diseases, Duke-NUS Graduate Medical School, 8 College Road, Singapore, 169857, Singapore.
  • 4 Computational Biology, Genome Institute of Singapore, Singapore, 138672, Singapore.
  • 5 Department of Neurology, National Neuroscience Institute, 20 College Road, Singapore, 169856, Singapore.
  • 6 Stem Cell and Regenerative Biology, Genome Institute of Singapore, 60 Biopolis Street, Singapore, 138672, Singapore.
  • 7 Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117545, Singapore.
  • 8 Immunology programme, Life Sciences Institute, National University of Singapore, Singapore, 119077, Singapore.
  • 9 Infectious Diseases, Genome Institute of Singapore, Singapore, 138672, Singapore.
  • 10 London School of Hygiene & Tropical Medicine, London, WC1E 7HT, UK.
  • 11 Institute of Materials Research and Engineering (IMRE), A*STAR, Singapore, 138634, Singapore.
  • 12 Department of Materials Science and Engineering, National University of Singapore, Singapore, 117575, Singapore.
  • 13 GERMS Platform, Genome Institute of Singapore, Singapore, 138672, Singapore.
  • 14 Saw Swee Hock School of Public Health, National University of Singapore, Singapore, 117549, Singapore.
  • 15 Bioinformatics Institute (A*STAR), 30 Biopolis Street #07-01, Matrix, Singapore, 138671, Singapore. peterjb@bii.a-star.edu.sg.
  • 16 Program in Emerging Infectious Diseases, Duke-NUS Graduate Medical School, 8 College Road, Singapore, 169857, Singapore. october.sessions@duke-nus.edu.sg.
  • 17 Saw Swee Hock School of Public Health, National University of Singapore, Singapore, 117549, Singapore. october.sessions@duke-nus.edu.sg.
  • 18 Department of Pharmacy, National University of Singapore, Singapore, 117559, Singapore. october.sessions@duke-nus.edu.sg.
  • 19 Stem Cell and Regenerative Biology, Genome Institute of Singapore, Singapore, 138672, Singapore. wany@gis.a-star.edu.sg.
  • 20 School of Biological Sciences, Nanyang Technological University, Singapore, 637551, Singapore. wany@gis.a-star.edu.sg.
  • 21 Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117597, Singapore. wany@gis.a-star.edu.sg.
  • DOI: 10.1038/s41467-019-09391-8 PMID: 30926818

    摘要 Ai翻译

    Dengue (DENV) and Zika (ZIKV) viruses are clinically important members of the Flaviviridae family with an 11 kb positive strand RNA genome that folds to enable virus function. Here, we perform structure and interaction mapping on four DENV and ZIKV strains inside virions and in infected cells. Comparative analysis of SHAPE reactivities across serotypes nominates potentially functional regions that are highly structured, conserved, and contain low synonymous mutation rates. Interaction mapping by SPLASH identifies many pair-wise interactions, 40% of which form alternative structures, suggesting extensive structural heterogeneity. Analysis of shared interactions between serotypes reveals a conserved macro-organization whereby interactions can be preserved at physical locations beyond sequence identities. We further observe that longer-range interactions are preferentially disrupted inside cells, and show the importance of new interactions in virus fitness. These findings deepen our understanding of Flavivirus genome organization and serve as a resource for designing therapeutics in targeting RNA viruses.

    Keywords:dengue viruses; zika viruses; structure mapping

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    期刊名:Nature communications

    缩写:NAT COMMUN

    ISSN:N/A

    e-ISSN:2041-1723

    IF/分区:15.7/Q1

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