The zinc finger antiviral protein (ZAP) is a broad inhibitor of virus replication. Its best-characterized function is to bind CpG dinucleotides present in viral RNAs and, through the recruitment of TRIM25, KHNYN and other cofactors, target them for degradation or prevent their translation. The long and short isoforms of ZAP (ZAP-L and ZAP-S) have different intracellular localization and it is unclear how this regulates their antiviral activity against viruses with different sites of replication. Using ZAP-sensitive and ZAP-insensitive human immunodeficiency virus type I (HIV-1), which transcribe the viral RNA in the nucleus and assemble virions at the plasma membrane, we show that the catalytically inactive poly-ADP-ribose polymerase (PARP) domain in ZAP-L is essential for CpG-specific viral restriction. Mutation of a crucial cysteine in the C-terminal CaaX box that mediates S-farnesylation and, to a lesser extent, the residues in place of the catalytic site triad within the PARP domain, disrupted the activity of ZAP-L. Addition of the CaaX box to ZAP-S partly restored antiviral activity, explaining why ZAP-S lacks antiviral activity for CpG-enriched HIV-1 despite conservation of the RNA-binding domain. Confocal microscopy confirmed the CaaX motif mediated localization of ZAP-L to vesicular structures and enhanced physical association with intracellular membranes. Importantly, the PARP domain and CaaX box together jointly modulate the interaction between ZAP-L and its cofactors TRIM25 and KHNYN, implying that its proper subcellular localisation is required to establish an antiviral complex. The essential contribution of the PARP domain and CaaX box to ZAP-L antiviral activity was further confirmed by inhibition of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) replication, which replicates in double-membrane vesicles derived from the endoplasmic reticulum. Thus, compartmentalization of ZAP-L on intracellular membranes provides an essential effector function in ZAP-L-mediated antiviral activity against divergent viruses with different subcellular replication sites. Author summary Cell-intrinsic antiviral factors, such as the zinc finger antiviral protein (ZAP), provide the first line of defence against viral pathogens. ZAP acts by selectively binding CpG dinucleotides in viral RNAs, leading to their degradation or translation inhibition. Here, we show that the ability to target these foreign elements is not only dependent on ZAP’s N-terminal RNA-binding domain, but additional determinants in the central and C-terminal regions also regulate this process. The PARP domain and its associated CaaX box, are crucial for ZAP’s CpG-specific activity and required for optimal binding to the ZAP cofactors TRIM25 and KHNYN. Furthermore, a CaaX box, known to mediate post-translational modification by a hydrophobic S-farnesyl group, caused re-localization of ZAP from the cytoplasm and increased its association with intracellular membranes. The distribution of the long isoform of ZAP to intracellular membranes was essential for inhibition of both a ZAP-sensitized HIV-1 and SARS-CoV-2. Our work unveils how the determinants outside the RNA-binding domain assist ZAP’s antiviral activity and highlights the role of S-farnesylation and membrane association in this process.
【초록키워드】 Structure, SARS-CoV-2, coronavirus, Antiviral, translation, antiviral activity, virus, RNAs, RNA, Endoplasmic reticulum, Replication, Protein, Microscopy, HIV-1, Factors, membrane, ZAP, virus replication, PARP, Viral RNA, Degradation, recruitment, Human immunodeficiency virus, distribution, binding, CpG, association, Interaction, regulate, cytoplasm, cysteine, cofactor, determinant, post-translational modification, acute respiratory syndrome, type I, complex, residue, domain, catalytic site, hydrophobic, plasma membrane, virion, nucleus, viral pathogens, membranes, element, motif, polymerase, TRIM25, dinucleotide, isoform, Vesicle, Prevent, physical, highlight, lack, caused, required, replicate, provide, in viral, modulate, dependent on, restored, C-terminal, inactive, assist, subcellular, broad inhibitor, C-terminal region, catalytically, KHNYN, N-terminal RNA-binding domain, 【제목키워드】 antiviral activity, Replication, ZAP, RNA virus, isoform,