Literature DB >> 32188627

Structural Biology of the Enterovirus Replication-Linked 5'-Cloverleaf RNA and Associated Virus Proteins.

Steven M Pascal1, Ravindranath Garimella2, Meghan S Warden2, Komala Ponniah2.   

Abstract

Although enteroviruses are associated with a wide variety of diseases and conditions, their mode of replication is well conserved. Their genome is carried as a single, positive-sense RNA strand. At the 5' end of the strand is an approximately 90-nucleotide self-complementary region called the 5' cloverleaf, or the oriL. This noncoding region serves as a platform upon which host and virus proteins, including the 3B, 3C, and 3D virus proteins, assemble in order to initiate replication of a negative-sense RNA strand. The negative strand in turn serves as a template for synthesis of multiple positive-sense RNA strands. Building on structural studies of individual RNA stem-loops, the structure of the intact 5' cloverleaf from rhinovirus has recently been determined via nuclear magnetic resonance/small-angle X-ray scattering (NMR/SAXS)-based methods, while structures have also been determined for enterovirus 3A, 3B, 3C, and 3D proteins. Analysis of these structures, together with structural and modeling studies of interactions between host and virus proteins and RNA, has begun to provide insight into the enterovirus replication mechanism and the potential to inhibit replication by blocking these interactions.
Copyright © 2020 American Society for Microbiology.

Keywords:  SAXS; X-ray crystallography; enterovirus; nuclear magnetic resonance; picornavirus; structure; viral replication

Mesh:

Substances:

Year:  2020        PMID: 32188627      PMCID: PMC7399744          DOI: 10.1128/MMBR.00062-19

Source DB:  PubMed          Journal:  Microbiol Mol Biol Rev        ISSN: 1092-2172            Impact factor:   11.056


  128 in total

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Journal:  J Mol Biol       Date:  2013-04-11       Impact factor: 5.469

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Journal:  J Biomol NMR       Date:  2008-09-12       Impact factor: 2.835

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Journal:  J Virol       Date:  1992-04       Impact factor: 5.103

9.  Rhinovirus 3C protease facilitates specific nucleoporin cleavage and mislocalisation of nuclear proteins in infected host cells.

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Journal:  PLoS One       Date:  2013-08-07       Impact factor: 3.240

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  2 in total

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Authors:  Hailan Meng; Qi Wang; Meiling Liu; Ziwei Li; Xiaojing Hao; Di Zhao; Yaqin Dong; Shuang Liu; Feng Zhang; Jin Cui; Bo Ni; Hu Shan; Fuxiao Liu
Journal:  Front Microbiol       Date:  2022-08-17       Impact factor: 6.064

Review 2.  Rhinovirus Inhibitors: Including a New Target, the Viral RNA.

Authors:  Antonio Real-Hohn; Dieter Blaas
Journal:  Viruses       Date:  2021-09-07       Impact factor: 5.048

  2 in total

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