Abstract
Nonsense-mediated mRNA decay (NMD) is an evolutionarily conserved RNA decay mechanism that has emerged as a potent cell-intrinsic restriction mechanism of retroviruses and positive-strand RNA viruses. However, whether NMD is capable of restricting DNA viruses is not known. The DNA virus Kaposi’s sarcoma-associated herpesvirus (KSHV) is the etiological agent of Kaposi’s sarcoma and primary effusion lymphoma (PEL). Here, we demonstrate that NMD restricts KSHV lytic reactivation. Leveraging high-throughput transcriptomics we identify NMD targets transcriptome-wide in PEL cells and identify host and viral RNAs as substrates. Moreover, we identified an NMD-regulated link between activation of the unfolded protein response and transcriptional activation of the main KSHV transcription factor RTA, itself an NMD target. Collectively, our study describes an intricate relationship between cellular targets of an RNA quality control pathway and KSHV lytic gene expression, and demonstrates that NMD can function as a cell intrinsic restriction mechanism acting upon DNA viruses.
Highlights
Nonsense-mediated mRNA decay (NMD) is an evolutionarily conserved RNA decay mechanism that has emerged as a potent cell-intrinsic restriction mechanism of retroviruses and positive-strand RNA viruses
We have determined that NMD is a potent restriction mechanism against the DNA virus Kaposi’s sarcoma-associated herpesvirus (KSHV)
We find that siRNA-mediated silencing of the NMD factors UPF1 and UPF3X significantly enhances KSHV lytic reactivation in both iSLK.[219] and TRExBCBL1-RTA cells
Summary
Nonsense-mediated mRNA decay (NMD) is an evolutionarily conserved RNA decay mechanism that has emerged as a potent cell-intrinsic restriction mechanism of retroviruses and positive-strand RNA viruses. Our study describes an intricate relationship between cellular targets of an RNA quality control pathway and KSHV lytic gene expression, and demonstrates that NMD can function as a cell intrinsic restriction mechanism acting upon DNA viruses. The best-characterized substrates of NMD are mRNAs that harbor normal or premature termination codons (PTCs) located 50–55 nucleotides (nt) upstream of an exon–exon junction[4]. Additional substrates such as mRNAs that contain upstream open read frames (uORFs) and long 3′-untranslated regions (UTRs) can be targeted[5,6,7,8]. Whether NMD functions as an antiviral defense mechanism against DNA viruses is not known
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