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      Dengue virus strain 2 capsid protein switches the annealing pathway and reduces intrinsic dynamics of the conserved 5’ untranslated region

      research-article
      a , b , c , c , b , c , b , c
      RNA Biology
      Taylor & Francis
      RNA chaperone, FRET-FCS, genome circularization, RNA replication, kissing loop

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          ABSTRACT

          The capsid protein of dengue virus strain 2 (DENV2C) promotes nucleic acid structural rearrangements using chaperone activity. However, the role of DENV2C during the interaction of RNA elements in the conserved 5’ untranslated region (5’UTR) to the 3’ untranslated region (3’UTR) is still unclear. Thus, we investigated the effect of DENV2C on the annealing mechanism of two RNA hairpin elements from the 5’UTR to their complementary sequences during (+)/(-) ds-RNAformation and (+) RNA circularization. DENV2C was found to switch the annealing pathway for RNA elements involved in (+)/(-) ds-RNA formation, but not for RNA elements related to (+) RNA circularization. In addition, we also determined that DENV2C modulates intrinsic dynamics and reduces kinetically trapped unfavourable conformations of the 5’UTR sequence. Thus, our results provide mechanistic insights by which DENV2C chaperones the interactions between RNA elements at the 5’ and 3’ ends during genome recombination, a prerequisite for DENV replication.

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          Dengue virus pathogenesis: an integrated view.

          Much remains to be learned about the pathogenesis of the different manifestations of dengue virus (DENV) infections in humans. They may range from subclinical infection to dengue fever, dengue hemorrhagic fever (DHF), and eventually dengue shock syndrome (DSS). As both cell tropism and tissue tropism of DENV are considered major determinants in the pathogenesis of dengue, there is a critical need for adequate tropism assays, animal models, and human autopsy data. More than 50 years of research on dengue has resulted in a host of literature, which strongly suggests that the pathogenesis of DHF and DSS involves viral virulence factors and detrimental host responses, collectively resulting in abnormal hemostasis and increased vascular permeability. Differential targeting of specific vascular beds is likely to trigger the localized vascular hyperpermeability underlying DSS. A personalized approach to the study of pathogenesis will elucidate the basis of individual risk for development of DHF and DSS as well as identify the genetic and environmental bases for differences in risk for development of severe disease.
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            The role of structural disorder in the function of RNA and protein chaperones.

            Chaperones are highly sophisticated protein machines that assist the folding of RNA molecules or other proteins. Their function is generally thought to require a fine-tuned and highly conserved structure: despite the recent recognition of the widespread occurrence of structural disorder in the proteome, this structural trait has never been generally considered in molecular chaperones. In this review we give evidence for the prevalence of functional regions without a well-defined 3-D structure in RNA and protein chaperones. By considering a variety of individual examples, we suggest that the structurally disordered chaperone regions either function as molecular recognition elements that act as solubilizers or locally loosen the structure of the kinetically trapped folding intermediate via transient binding to facilitate its conformational search. The importance of structural disorder is underlined by a predictor of natural disordered regions, which shows an extremely high proportion of such regions, unparalleled in any other protein class, within RNA chaperones: 54.2% of their residues fall into disordered regions and 40% fall within disordered regions longer than 30 consecutive residues. Structural disorder also prevails in protein chaperones, for which frequency values are 36.7% and 15%, respectively. In keeping with these and other details, a novel "entropy transfer" model is presented to account for the mechanistic role of structural disorder in chaperone function.
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              RNA chaperones and the RNA folding problem.

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                Author and article information

                Journal
                RNA Biol
                RNA Biol
                RNA Biology
                Taylor & Francis
                1547-6286
                1555-8584
                7 January 2021
                2021
                7 January 2021
                : 18
                : 5 , Special Issue: RNA in immunity, infection and immune diseases
                : 718-731
                Affiliations
                [a ]NUS Graduate School for integrative Sciences and Engineering Programme, National University of Singapore; , Singapore
                [b ]Centre for Bioimaging Sciences, National University of Singapore; , Singapore, Singapore
                [c ]Department of Biological Sciences, National University of Singapore; , Singapore, Singapore
                Author notes
                CONTACT Kamal K. Sharma dbskks@ 123456nus.edu.sg
                Thorsten Wohland twohland@ 123456nus.edu.sg Centre for Bioimaging Sciences, National University of Singapore; , Singapore117557, Singapore
                Author information
                https://orcid.org/0000-0002-4235-0071
                Article
                1860581
                10.1080/15476286.2020.1860581
                8078513
                33406991
                62ea2658-734a-4aed-a23b-a94ae8652a48
                © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                Page count
                Figures: 7, Tables: 2, References: 64, Pages: 14
                Categories
                Research Article
                Research Paper

                Molecular biology
                rna chaperone,fret-fcs,genome circularization,rna replication,kissing loop
                Molecular biology
                rna chaperone, fret-fcs, genome circularization, rna replication, kissing loop

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