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Asesino: a nucleus-forming phage that lacks PhuZ.
Prichard, Amy; Sy, Annika; Meyer, Justin; Villa, Elizabeth; Pogliano, Joe.
Afiliación
  • Prichard A; School of Biological Sciences, University of California San Diego, La Jolla, CA 92093, USA.
  • Sy A; School of Biological Sciences, University of California San Diego, La Jolla, CA 92093, USA.
  • Meyer J; School of Biological Sciences, University of California San Diego, La Jolla, CA 92093, USA.
  • Villa E; School of Biological Sciences, University of California San Diego, La Jolla, CA 92093, USA.
  • Pogliano J; Howard Hughes Medical Institute, University of California San Diego, La Jolla, CA 92093, USA.
bioRxiv ; 2024 May 11.
Article en En | MEDLINE | ID: mdl-38766163
ABSTRACT
As nucleus-forming phages become better characterized, understanding their unifying similarities and unique differences will help us understand how they occupy varied niches and infect diverse hosts. All identified nucleus-forming phages fall within the proposed Chimalliviridae family and share a core genome of 68 unique genes including chimallin, the major nuclear shell protein. A well-studied but non-essential protein encoded by many nucleus-forming phages is PhuZ, a tubulin homolog which aids in capsid migration, nucleus rotation, and nucleus positioning. One clade that represents 24% of all currently known chimalliviruses lacks a PhuZ homolog. Here we show that Erwinia phage Asesino, one member of this PhuZ-less clade, shares a common overall replication mechanism with other characterized nucleus-forming phages despite lacking PhuZ. We show that Asesino replicates via a phage nucleus that encloses phage DNA and partitions proteins in the nuclear compartment and cytoplasm in a manner similar to previously characterized nucleus-forming phages. Consistent with a lack of PhuZ, however, we did not observe active positioning or rotation of the phage nucleus within infected cells. These data show that some nucleus-forming phages have evolved to replicate efficiently without PhuZ, providing an example of a unique variation in the nucleus-based replication pathway.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos