Genome organization and interaction with capsid protein in a multipartite RNA virus.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
19 05 2020
Historique:
pubmed: 3 5 2020
medline: 11 8 2020
entrez: 3 5 2020
Statut: ppublish

Résumé

We report the asymmetric reconstruction of the single-stranded RNA (ssRNA) content in one of the three otherwise identical virions of a multipartite RNA virus, brome mosaic virus (BMV). We exploit a sample consisting exclusively of particles with the same RNA content-specifically, RNAs 3 and 4-assembled in planta by agrobacterium-mediated transient expression. We find that the interior of the particle is nearly empty, with most of the RNA genome situated at the capsid shell. However, this density is disordered in the sense that the RNA is not associated with any particular structure but rather, with an ensemble of secondary/tertiary structures that interact with the capsid protein. Our results illustrate a fundamental difference between the ssRNA organization in the multipartite BMV viral capsid and the monopartite bacteriophages MS2 and Qβ for which a dominant RNA conformation is found inside the assembled viral capsids, with RNA density conserved even at the center of the particle. This can be understood in the context of the differing demands on their respective lifecycles: BMV must package separately each of several different RNA molecules and has been shown to replicate and package them in isolated, membrane-bound, cytoplasmic complexes, whereas the bacteriophages exploit sequence-specific "packaging signals" throughout the viral RNA to package their monopartite genomes.

Identifiants

pubmed: 32358197
pii: 1915078117
doi: 10.1073/pnas.1915078117
pmc: PMC7245085
doi:

Substances chimiques

Capsid Proteins 0
Qbeta ribonucleic acid 0
RNA, Viral 0

Banques de données

PDB
['6VOC']

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

10673-10680

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI094386
Pays : United States
Organisme : NIDCR NIH HHS
ID : R01 DE025567
Pays : United States
Organisme : NIDCR NIH HHS
ID : R01 DE028583
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM071940
Pays : United States

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

Christian Beren (C)

Department of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095.

Yanxiang Cui (Y)

California NanoSystems Institute, University of California, Los Angeles, CA 90095.

Antara Chakravarty (A)

Department of Microbiology and Plant Pathology, University of California, Riverside, CA 92521.

Xue Yang (X)

California NanoSystems Institute, University of California, Los Angeles, CA 90095.
Department of Microbiology, Immunology & Molecular Genetics, University of California, Los Angeles, CA 90095.

A L N Rao (ALN)

Department of Microbiology and Plant Pathology, University of California, Riverside, CA 92521; arao@ucr.edu Hong.Zhou@UCLA.edu gelbart@chem.ucla.edu.

Charles M Knobler (CM)

Department of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095.

Z Hong Zhou (ZH)

California NanoSystems Institute, University of California, Los Angeles, CA 90095; arao@ucr.edu Hong.Zhou@UCLA.edu gelbart@chem.ucla.edu.
Department of Microbiology, Immunology & Molecular Genetics, University of California, Los Angeles, CA 90095.

William M Gelbart (WM)

Department of Chemistry & Biochemistry, University of California, Los Angeles, CA 90095; arao@ucr.edu Hong.Zhou@UCLA.edu gelbart@chem.ucla.edu.
California NanoSystems Institute, University of California, Los Angeles, CA 90095.
Molecular Biology Institute, University of California, Los Angeles, CA 90095.

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Classifications MeSH