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Replication competent HIV-guided CRISPR screen identifies antiviral factors including targets of the accessory protein Nef

Title: Replication competent HIV-guided CRISPR screen identifies antiviral factors including targets of the accessory protein Nef
Authors: Prelli Bozzo, Caterina; Laliberté, Alexandre; De Luna, Aurora; Pastorio, Chiara; Regensburger, Kerstin; Krebs, Stefan; Graf, Alexander; Blum, Helmut; Volcic, Meta; Sparrer, Konstantin M. J.; Kirchhoff, Frank
Publisher Information: Universität Ulm
Publication Year: 2024
Collection: OPARU (OPen Access Repository of Ulm University)
Subject Terms: Innate immunity; Virology
Description: Innate antiviral factors are essential for effective defense against viral pathogens. However, the identity of major restriction mechanisms remains elusive. Current approaches to discover antiviral factors usually focus on the initial steps of viral replication and are limited to a single round of infection. Here, we engineered libraries of >1500 replication-competent HIV-1 constructs each expressing a single gRNAs to target >500 cellular genes for virus-driven discovery of antiviral factors. Passaging in CD4 + T cells robustly enriched HIV-1 encoding sgRNAs against GRN , CIITA , EHMT2 , CEACAM3 , CC2D1B and RHOA by >50-fold. Using an HIV-1 library lacking the accessory nef gene, we identified IFI16 as a Nef target. Functional analyses in cell lines and primary CD4 + T cells support that the HIV-driven CRISPR screen identified restriction factors targeting virus entry, transcription, release and infectivity. Our HIV-guided CRISPR technique enables sensitive discovery of physiologically relevant cellular defense factors throughout the entire viral replication cycle.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
DOI: 10.18725/OPARU-56409
Availability: https://doi.org/10.18725/OPARU-56409; http://nbn-resolving.de/urn:nbn:de:bsz:289-oparu-56484-0
Rights: http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.11E163AD
Database: BASE