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Biology subjects

Regensburger, K.

Publications and source records attributed to Regensburger, K..

2 recordsLinked to original sources

Human regnases are evolutionarily diversified antiviral restriction factors targeting viral RNA

Regnases regulate immune gene expression by degrading cellular mRNAs. Regnase-1 also targets viral RNA, but whether this activity is shared among other human Regnases remains unknown. Here, we systematically compared the antiviral properties of all four Regnases. Expression of Regnases-1-4 inhibited RNA viruses HIV-1, HIV-2, MLV, RSV, OC43 and SARS-CoV-2, but not DNA virus HSV-1. Depletion experiments demonstrated that endogenous Regnases restrict HIV-1 replication in a cell-type-dependent manner, with Regnase-1 and Regnase-4 exerting the strongest effects in T-cells and monocytes, and Regnase-2 and Regnase-3 in primary macrophages. All Regnases displayed signatures of positive selection, consistent with their roles as antiviral restriction factors, but only Regnase-1 and -4 were induced by interferons. Mechanistically, the antiviral activity of Regnases required an intact catalytic core, a CCCH zinc finger, and, in the case of Regnase-1, -2 and -3, a dimerisation motif (P/R). Chimeric Regnase-1 and Regnase-3 constructs suggested that differences in antiviral potency primarly reflect differences in RNA recognition rather than catalytic activity. Bicistronic reporter assays suggested that Regnase-1 and -4 exhibit broad targeting, whereas Regnases-2 and -3 display greater substrate selectivity and correlate in target specificity. Collectively, our findings establish Regnases as antiviral restriction factors with distinct viral RNA targeting specificities.

immunology↗

Traitor-virus-guided discovery of novel antiviral factors

Complex pathogen-host interactions govern the outcome of viral exposures but remain poorly understood because current methods to elucidate antiviral mechanisms are prone to artefacts and lack sensitivity. Here, we developed a virus-guided technology platform where the pathogen itself reveals its cellular opponents. To accomplish this, we engineered replication-competent HIV-1 expressing sgRNAs targeting potential antiviral genes in Cas9-expressing CD4+ T cells. Simultaneous analysis of HIV-1 constructs targeting >500 candidate genes revealed that sgRNAs against GRN, CIITA, EHMT2, CEACAM3, CC2D1B, RHOA and HMOX1 are strongly enriched over several rounds of replication. Overexpression and knock-out studies confirmed the antiretroviral activity of most factors but failed for some. Finally, we show that lack of the accessory nef gene increased enrichment of sgRNAs targeting SERINC5 and IFI16 demonstrating that this method allows identification of targets of accessory proteins. The versatile and effective HIV-guided CRISPR technology offers numerous possibilities for clarification of virus-host interactions and innate defense mechanisms.

microbiology↗