The CCCTC Binding Factor, CTRL2, Modulates Heterochromatin Deposition and the Establishment of Herpes Simplex Virus 1 Latency In Vivo

• Published in: Journal of virology Vol. 93; no. 13
• Main Authors: Washington, Shannan D, Singh, Pankaj, Johns, Richard N, Edwards, Terri G, Mariani, Michael, Frietze, Seth, Bloom, David C, Neumann, Donna M
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01-07-2019
• Subjects: Animals; CCCTC-Binding Factor - genetics; CCCTC-Binding Factor - metabolism; Chromatin - metabolism; Chromatin Assembly and Disassembly; Chromatin Immunoprecipitation; Disease Models, Animal; Epigenomics; Eye Infections - virology; Ganglia - virology; Gene Expression Regulation, Viral; Gene Silencing; Genome and Regulation of Viral Gene Expression; Genome, Viral; Herpes Simplex - virology; Herpesvirus 1, Human - genetics; Herpesvirus 1, Human - metabolism; Herpesvirus 4, Human - physiology; Herpesvirus 8, Human - physiology; Heterochromatin - metabolism; Mice; Mice, Inbred BALB C; Mice, Knockout; Virus Activation; Virus Latency - physiology; Virus Replication; CTRL2; HSV-1; latency; chromatin remodeling; CTCF; insulator; epigenetics; mouse ocular model
• ISSN: 0022-538X; 1098-5514
• DOI: 10.1128/JVI.00415-19

The cellular insulator protein CTCF plays a role in herpes simplex virus 1 (HSV-1) latency through the establishment and regulation of chromatin boundaries. We previously found that the CTRL2 regulatory element downstream from the latency-associated transcript (LAT) enhancer was bound by CTCF during latency and underwent CTCF eviction at early times postreactivation in mice latently infected with 17
+ virus. We also showed that CTRL2 was a functional enhancer-blocking insulator in both epithelial and neuronal cell lines. We hypothesized that CTRL2 played a direct role in silencing lytic gene expression during the establishment of HSV-1 latency. To test this hypothesis, we used a recombinant virus with a 135-bp deletion spanning only the core CTRL2 insulator domain (ΔCTRL2) in the 17
+ background. Deletion of CTRL2 resulted in restricted viral replication in epithelial cells but not neuronal cells. Following ocular infection, mouse survival decreased in the ΔCTRL2-infected cohort, and we found a significant decrease in the number of viral genomes in mouse trigeminal ganglia (TG) infected with ΔCTRL2, indicating that the CTRL2 insulator was required for the efficient establishment of latency. Immediate early (IE) gene expression significantly increased in the number of ganglia infected with ΔCTRL2 by 31 days postinfection relative to the level with 17
+ infection, indicating that deletion of the CTRL2 insulator disrupted the organization of chromatin domains during HSV-1 latency. Finally, chromatin immunoprecipitation with high-throughput sequencing (ChIP-seq) analyses of TG from ΔCTRL2-infected mice confirmed that the distribution of the repressive H3K27me3 (histone H3 trimethylated at K27) mark on the ΔCTRL2 recombinant genomes was altered compared to that of the wild type, indicating that the CTRL2 site modulates the repression of IE genes during latency.
It is becoming increasingly clear that chromatin insulators play a key role in the transcriptional control of DNA viruses. The gammaherpesviruses Epstein-Barr virus (EBV) and Kaposi's sarcoma-associated herpesvirus (KSHV) utilize chromatin insulators to order protein recruitment and dictate the formation of three-dimensional DNA loops that spatially control transcription and latency. The contribution of chromatin insulators in alphaherpesvirus transcriptional control is less well understood. The work presented here begins to bridge that gap in knowledge by showing how one insulator site in HSV-1 modulates lytic gene transcription and heterochromatin deposition as the HSV-1 genome establishes latency.