PP2A1 Binding, Cell Transducing and Apoptotic Properties of Vpr77-92: A New Functional Domain of HIV-1 Vpr Proteins

23Citations
Citations of this article
20Readers
Mendeley users who have this article in their library.

Abstract

Background: The hallmark of HIV-1 pathogenesis is the progressive CD4+ T cell depletion and high propensity of CD4+ T cells to apoptosis. HIV-1 viral protein R (Vpr) is a major pro-apoptotic gene product. A first Vpr-mediated apoptotic mechanism that requires a physical interaction of HIV-1 Vpr71-82 mitochondriotoxic domain containing the conserved sequence 71-HFRIGCRHSRIG-82 with the Adenine Nucleotide Translocator (ANT) has been characterized. The family of Ser/Thr protein phosphatase PP2A interacts with several viral proteins to regulate cell growth and apoptotic pathways. Previous studies based on yeast two hybrid assays and mutational experiments indicated that PP2A1 is involved in the induction of G2 arrest by HIV-1 Vpr. Principal Findings: Experiments combining pull-down, cell penetration and apoptosis analyses in distinct human cells indicate that the PP2A1 binding sequence from Vpr77-92 is a new cell penetrating apoptotic sequence. We also found that the I84P mutation or the IIQ/VTR83-85 and T89A substitutions in the Vpr77-92 sequence prevent PP2A1 binding, cell penetration and apoptosis. In addition the double R77A and R80A mutation known to inactivate the mitochondriotoxic Vpr71-82 domain, has no effect on the biological properties of the Vpr77-92 domain. Conclusion: Together our data provide evidence for the first time that the Vpr77-92 sequence delineates a biological active domain of Vpr with PP2A1 binding and pro-apopototic capacities and, it is conceivable that this cell penetrating sequence may account for the Vpr internalization in uninfected cells. Finally, our data also implicate the existence of two partially overlapping pro-apoptotic domains in the Vpr C-terminal part, a redundancy that represents a new approach to address the question of biological relevance of HIV-1 Vpr. In this context, future studies will be required to determine the functional relevance of the Vpr77-92 domain in full length Vpr protein and also in entire HIV provirus. © 2010 Godet et al.

Cite

CITATION STYLE

APA

Godet, A. N., Guergnon, J., Croset, A., Cayla, X., Falanga, P. B., Colle, J. H., & Garcia, A. (2010). PP2A1 Binding, Cell Transducing and Apoptotic Properties of Vpr77-92: A New Functional Domain of HIV-1 Vpr Proteins. PLoS ONE, 5(11). https://doi.org/10.1371/journal.pone.0013760

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free