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Sequential membrane- and protein-bound organelles compartmentalize genomes during phage infection

Eukaryotic viruses assemble compartments required for genome replication, but no such organelles are known to be essential for prokaryotic viruses. Bacteriophages of the family Chimalliviridae sequester their genomes within a phage-generated organelle, the phage nucleus, which is enclosed by a latti...

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Detalles Bibliográficos
Autores principales: Armbruster, Emily G., Lee, Jina, Hutchings, Joshua, VanderWal, Arica R., Enustun, Eray, Adler, Benjamin A., Aindow, Ann, Deep, Amar, Rodriguez, Zaida K., Morgan, Chase J., Ghassemian, Majid, Charles, Emeric, Cress, Brady F., Savage, David F., Doudna, Jennifer A., Pogliano, Kit, Corbett, Kevin D., Villa, Elizabeth, Pogliano, Joe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541120/
https://www.ncbi.nlm.nih.gov/pubmed/37781618
http://dx.doi.org/10.1101/2023.09.20.558163
Descripción
Sumario:Eukaryotic viruses assemble compartments required for genome replication, but no such organelles are known to be essential for prokaryotic viruses. Bacteriophages of the family Chimalliviridae sequester their genomes within a phage-generated organelle, the phage nucleus, which is enclosed by a lattice of viral protein ChmA. Using the dRfxCas13d-based knockdown system CRISPRi-ART, we show that ChmA is essential for the E. coli phage Goslar life cycle. Without ChmA, infections are arrested at an early stage in which the injected phage genome is enclosed in a membrane-bound vesicle capable of gene expression but not DNA replication. Not only do we demonstrate that the phage nucleus is essential for genome replication, but we also show that the Chimalliviridae early phage infection (EPI) vesicle is a transcriptionally active, phage-generated organelle.