Project III: Vpr/GR (Aim lla)Project Leader: Velpandi Ayyavoo, PhDVpr is involved in nuclear localization and trafficking of the provirus into the nucleus of non-dividing cells,such as macrophages and dendritic cells244'245. Though Vpr is not absolutely essential for T cell infection, thepresence of Vpr enhances viral replication in T cells and activates latently infected and resting T cells. Vprenhances viral replication by altering transport into the nucleus and by facilitating changes in cellular functionsand the HIV-1 life cycle246. Virion-associated Vpr transactivates HIV-1 long terminal repeat sequences (LTR)and activates virus transcription prior to de novo synthesis of other viral proteins through an interaction withglucocorticoid receptor (GR). Recent studies using Vpr mutants by us and other investigators have clearlydemonstrated that Vpr interacts with GR through a highly conserved leucine-rich GR signature motif in Vpr,suggesting that the Vpr/GR interaction is specific129' . Furthermore, Vpr/GR interaction and its subsequentfunctional regulations are independent of other Vpr functions such as cell cycle arrest. This suggests apossible role for the GR pathway in Vpr-mediated virus replication. In work done by our laboratory, the cellulardysregulation by Vpr was found to relate to the ability of Vpr to suppress NF-kB activity through the induction ofIkB transcription in a manner similar to glucocorticoids248. The regulation of NF-kB by Vpr suggests a molecularbasis for the cellular effects of Vpr and supports the possibility that this gene product might mediate someaspects of viral pathogenesis. Taken together, these results suggest that Vpr, via the GR pathway, could, inpart, contribute to viral replication and disease progression. Toward accomplishing Aim Ha, Project III will workclosely with the Cellular and Single Particle Imaging Core to further characterize the interaction between Vprand GR in cells and will begin expression studies to identify methods and domains of the GR protein mostsuitable for structural determination.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Specialized Center (P50)
Project #
1P50GM082251-01
Application #
7507623
Study Section
Special Emphasis Panel (ZRG1-AARR-A (40))
Project Start
2007-08-27
Project End
2012-07-31
Budget Start
2007-08-27
Budget End
2008-07-31
Support Year
1
Fiscal Year
2007
Total Cost
$157,311
Indirect Cost
Name
University of Pittsburgh
Department
Type
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
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