sq-23377 and prostratin

Viral-host interactomes map the complex architecture of an evolved arms race during host cell invasion. mRNA and protein interactomes reveal elaborate targeting schemes, yet evidence is lacking for genetic coupling that results in the co-regulation of promoters. Here we compare viral and human promoter sequences and expression to test whether genetic coupling exists and investigate its phenotypic consequences. We show that viral-host co-evolution is imprinted within promoter gene sequences before transcript or protein interactions. Co-regulation of human immunodeficiency virus (HIV) and human C-X-C chemokine receptor-4 (CXCR4) facilitates migration of infected cells. Upon infection, HIV can actively replicate or remain dormant. Migrating infected cells reactivate from dormancy more than non-migrating cells and exhibit differential migration-reactivation responses to drugs. Cells producing virus pose a risk for reinitiating infection within niches inaccessible to drugs, and tuning viral control of migration and reactivation improves strategies to eliminate latent HIV. Viral-host genetic coupling establishes a mechanism for synchronizing transcription and guiding potential therapies.

Topics: CD4-Positive T-Lymphocytes; Cell Movement; Depsipeptides; Gene Expression Regulation; HIV Long Terminal Repeat; HIV-1; HL-60 Cells; Host-Pathogen Interactions; Humans; Hydroxamic Acids; Indoles; Ionomycin; Jurkat Cells; Panobinostat; Phorbol Esters; Primary Cell Culture; Promoter Regions, Genetic; Receptors, CXCR4; Tamoxifen; tat Gene Products, Human Immunodeficiency Virus; Transcription, Genetic; Tumor Necrosis Factor-alpha; Virus Activation; Virus Latency; Vorinostat