Wang X, Singh S, Jung HY, Yang G, Jun S, Sastry KJ, Park JI

Viral pathogens utilize host cell machinery for their benefits. Herein, we identify that HIV-1 viral protein R (Vpr) negatively modulates telomerase activity. Telomerase enables stem and cancer cells to evade cell senescence by adding telomeric sequences to the ends of chromosomes. We found that Vpr inhibited telomerase activity by downregulating ...

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TERT protein, a catalytic subunit of telomerase. As a molecular adaptor, Vpr enhanced the interaction between TERT and the VPRBP substrate receptor of DYRK2-associated EDD-DDB1-VPRBP E3 ligase complex, resulting in increased ubiquitination of TERT. In contrast, the Vpr mutant identified in HIV-1-infected long-term nonprogressors failed to promote TERT destabilization. Our results suggest that Vpr inhibits telomerase activity by hijacking the host E3 ligase complex, and propose the novel molecular mechanism of telomerase deregulation in possibly HIV-1 pathogenesis.

Date: Apr. 23, 2013

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