Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.596569
Title: The role of p2 in protein-RNA interactions of HIV
Author: Bennett, N.
Awarding Body: University of Cambridge
Current Institution: University of Cambridge
Date of Award: 2004
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Abstract:
The two subtypes of the Human Immunodeficiency Virus, HIV-1 and HIV-2, differ in the way that they package their genomic RNA with the structural Gag protein. HIV-1 packages its genomic RNA predominantly in a trans manner, and can cross-package HIV-2 RNA in co-transfections. Conversely, HIV-2 is not capable of packaging HIV-1 RNA reciprocally, and packages its own RNA using a co-translational mechanism. Chimeric viruses where the RNA-binding domain of HIV-1 is substituted into the structural of Gag protein of HIV-2 appear to transfer the trans packaging phenotype, but this function is only maximally present when the adjacent p2 peptide is also included. The aim of the work presented here was to investigate possible direct and indirect effects of the p2 domain in RNA-protein capture in HIV-1 and HIV-2. Chimeric Gag proteins were expressed using bacterial systems and their interaction with in vitro transcribed RNA of the HIV leader sequences investigated using GST-Pulldown assays, UV-crosslinking and mobility shift assays. Evidence is presented that is consistent with a complex and possibly cooperative binding interaction occurring between Gag and the packaged RNA, which correlates to some extent with the presence of the p2 domain. The subcellular location of the Gag protein was investigated using transfection with Gag-expressing and viral constructs, following by confocal microscopy of the immunostained cells, and no difference was found that could be attributed to the p2 domain. Additionally, the replication characteristics of the chimeric viruses were examined in short and long term culture. All chimeric viruses were defective in short term culture, but one culture did produce a replication-competent strain on long-term passage. This strain had wild type replication kinetics, and sequencing of the revertant virus revealed a single-base substitution in the highly basic region of the MA domain of Gag.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.596569  DOI: Not available
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