Cellular microRNA and P bodies modulate host-HIV-1 interactions
Department of Biochemistry and Molecular Pharmacology; Program in Gene Function and Expression
Life Sciences | Medicine and Health Sciences
MicroRNAs (miRNAs), approximately 22 nt noncoding RNAs, assemble into RNA-induced silencing complexes (RISCs) and localize to cytoplasmic substructures called P bodies. Dictated by base-pair complementarity between miRNA and a target mRNA, miRNAs specifically repress posttranscriptional expression of several mRNAs. Here we report that HIV-1 mRNA interacts with RISC proteins and that disrupting P body structures enhances viral production and infectivity. In HIV-1-infected human T lymphocytes, we identified a highly abundant miRNA, miR-29a, which specifically targets the HIV-1 3'UTR region. Inhibiting miR-29a enhanced HIV-1 viral production and infectivity, whereas expressing a miR-29 mimic suppressed viral replication. We also found that specific miR-29a-HIV-1 mRNA interactions enhance viral mRNA association with RISC and P body proteins. Thus we provide an example of a single host miRNA regulating HIV-1 production and infectivity. These studies highlight the significance of miRNAs and P bodies in modulating host cell interactions with HIV-1 and possibly other viruses.
DOI of Published Version
Mol Cell. 2009 Jun 26;34(6):696-709. Link to article on publisher's site
Nathans RS, Chu C, Serquina AK, Lu C, Cao H, Rana TM. (2009). Cellular microRNA and P bodies modulate host-HIV-1 interactions. Morningside Graduate School of Biomedical Sciences Student Publications. https://doi.org/10.1016/j.molcel.2009.06.003. Retrieved from https://escholarship.umassmed.edu/gsbs_sp/1619