生物
噬菌体
基因组
DNA
病毒学
噬菌体展示
清脆的
噬菌体
分子生物学
细胞生物学
遗传学
基因
大肠杆菌
抗体
作者
Deepto Mozumdar,Andrea Fossati,Erica Stevenson,Jingwen Guan,Eliza Nieweglowska,Sanjana Rao,David A. Agard,Danielle L. Swaney,Joseph Bondy‐Denomy
标识
DOI:10.1016/j.chom.2024.05.016
摘要
Viral genomes are most vulnerable to cellular defenses at the start of the infection. A family of jumbo phages related to phage ΦKZ, which infects Pseudomonas aeruginosa, assembles a protein-based phage nucleus to protect replicating phage DNA, but how it is protected prior to phage nucleus assembly is unclear. We find that host proteins related to membrane and lipid biology interact with injected phage protein, clustering in an early phage infection (EPI) vesicle. The injected virion RNA polymerase (vRNAP) executes early gene expression until phage genome separation from the vRNAP and the EPI vesicle, moving into the nascent proteinaceous phage nucleus. Enzymes involved in DNA replication and CRISPR/restriction immune nucleases are excluded by the EPI vesicle. We propose that the EPI vesicle is rapidly constructed with injected phage proteins, phage DNA, host lipids, and host membrane proteins to enable genome protection, early transcription, localized translation, and to ensure faithful genome transfer to the proteinaceous nucleus.
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