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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...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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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 |
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author | 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 |
author_facet | 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 |
author_sort | Armbruster, Emily G. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10541120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105411202023-10-01 Sequential membrane- and protein-bound organelles compartmentalize genomes during phage infection 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 bioRxiv Article 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. Cold Spring Harbor Laboratory 2023-09-21 /pmc/articles/PMC10541120/ /pubmed/37781618 http://dx.doi.org/10.1101/2023.09.20.558163 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article 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 Sequential membrane- and protein-bound organelles compartmentalize genomes during phage infection |
title | Sequential membrane- and protein-bound organelles compartmentalize genomes during phage infection |
title_full | Sequential membrane- and protein-bound organelles compartmentalize genomes during phage infection |
title_fullStr | Sequential membrane- and protein-bound organelles compartmentalize genomes during phage infection |
title_full_unstemmed | Sequential membrane- and protein-bound organelles compartmentalize genomes during phage infection |
title_short | Sequential membrane- and protein-bound organelles compartmentalize genomes during phage infection |
title_sort | sequential membrane- and protein-bound organelles compartmentalize genomes during phage infection |
topic | Article |
url | 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 |
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