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Thesis Defense Announcement
To:  The George Mason University Community
Candidate: Yao Akpamagbo

Program: M.S. in Biology



Date:   Wednesday August 24, 2016

Time:   11:00 am

Place:  George Mason University
             Science & Technology Campus<http://www.gmu.edu/resources/welcome/Directions-to-GMU.html>

             Bull Run Hall, Room 246



Title: "Transcription and Chromatin Analysis of Human Retroviruses"

Thesis Director: Dr. Fatah Kashanchi
Thesis Committee:  Dr. Karl Fryxell, Dr. Yuntao Wu

A copy of the thesis will be available in the Gateway Library.  All are invited to attend the defense.

ABSTRACT
During HIV infection, a provirus is integrated into the host genome where it is protected from transcription activators resulting in viral latency. Cellular long non-coding RNAs (lncRNA) and chromatin remodeling complexes (CRC) have recently emerged as key regulators in inhibitory pathways of infected cells. Here, we studied the activity of transcription inhibitors in HIV-infected cells to demonstrate that a novel HIV-1 RNA transcript, TAR-gag, is involved in HIV-1 latency. We also described a PBAF complex found only in HIV cells.  Our results suggest that transcription inhibitors, CR8#13 and F07#13, independently regulate transcription machinery in infected cells via the pTEF-b complex. We also observed the presence of a BAF 170 complex only found in HIV-infected cells. The results indicate that a component of the pTEF-b complex, cdk9, phosphorylates both activator and inhibitor forms of BAF, and PBAF in the same cell. We then showed that TAR-gag is bound to the msin3A/HDAC CRC. Additionally, treatment of HIV-infected cells with F07#13 favored an interaction between TAR-gag, HDAC and PIWI proteins, whereas CR8#13 favored an interaction between TAR-gag, HDAC and mSin3A proteins. Given that TAR-gag is not translated and is increased by HIV transcription inhibitors in T-cells, the data suggest that it is a viral non-coding RNA that contributes to viral latency.

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