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Title: Structure mapping of dengue and Zika viruses reveals functional long-range interactions
Authors: Huber, R.G.
Lim, X.N.
Ng, W.C.
Sim, A.Y.L.
Poh, H.X.
Shen, Y.
Lim, S.Y.
Sundstrom, K.B.
Sun, X.
Aw, J.G.
Too, H.K. 
Boey, P.H. 
Wilm, A.
Chawla, T.
Choy, M.M.
Jiang, L.
de Sessions, P.F.
Loh, X.J. 
Alonso, S. 
Hibberd, M.
Nagarajan, N.
Ooi, E.E. 
Bond, P.J.
Sessions, O.M. 
Wan, Y. 
Issue Date: 2019
Publisher: Nature Publishing Group
Citation: Huber, R.G., Lim, X.N., Ng, W.C., Sim, A.Y.L., Poh, H.X., Shen, Y., Lim, S.Y., Sundstrom, K.B., Sun, X., Aw, J.G., Too, H.K., Boey, P.H., Wilm, A., Chawla, T., Choy, M.M., Jiang, L., de Sessions, P.F., Loh, X.J., Alonso, S., Hibberd, M., Nagarajan, N., Ooi, E.E., Bond, P.J., Sessions, O.M., Wan, Y. (2019). Structure mapping of dengue and Zika viruses reveals functional long-range interactions. Nature Communications 10 (1) : 1408. ScholarBank@NUS Repository.
Rights: Attribution 4.0 International
Abstract: 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. © 2019, The Author(s).
Source Title: Nature Communications
ISSN: 2041-1723
DOI: 10.1038/s41467-019-09391-8
Rights: Attribution 4.0 International
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