EMD-21260

Single-particle
3.1 Å
EMD-21260 Deposition: 30/01/2020
Map released: 20/05/2020
Last modified: 06/03/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links

EMD-21260

icosahedral symmetry reconstruction of brome mosaic virus (RNA 3+4)

EMD-21260

Single-particle
3.1 Å
EMD-21260 Deposition: 30/01/2020
Map released: 20/05/2020
Last modified: 06/03/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Sample Organism: Brome mosaic virus
Sample: Brome mosaic virus
Fitted models: 6voc (Avg. Q-score: 0.417)

Deposition Authors: Beren C , Cui YX
Genome organization and interaction with capsid protein in a multipartite RNA virus.
Beren C , Cui Y , Chakravarty A , Yang X, Rao ALN , Knobler CM , Zhou ZH , Gelbart WM
(2020) PNAS , 117 , 10673 - 10680
PUBMED: 32358197
DOI: doi:10.1073/pnas.1915078117
ISSN: 1091-6490
ASTM: PNASA6
Abstract:
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.