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The molecular interactions of the Marek’s disease virus-encoded oncoprotein Meq

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Title: The molecular interactions of the Marek’s disease virus-encoded oncoprotein Meq
Authors: Green, James S.
Item Type: Thesis or dissertation
Abstract: Meq is a viral c-Jun analog and member of the AP-1 transcription factor family that acts as the primary oncoprotein encoded by Marek’s disease virus. Previous studies have shown that Meq interacts with a variety of proteins as part of its pivotal function in the development of Marek’s disease virus-induced lymphoma. The primary focus of this study was to identify the global interactome of the Meq oncoprotein. This was initially carried out by review of the Meq sequence and the subsequent identification of BATF and BATF3 as potential analogous partners. Interactions with novel proteins were also predicted based on the nature of charged interactions that mediate a leucine zipper dimerisation event. Furthermore, the Meq protein was used as bait in a yeast two-hybrid screen to produce a large data set of both known and novel interacting proteins. Interactions with JunB, JunD and CtBP1 were confirmed along with a set of novel proteins including Par-4, ATF3, RACK1, N4BP1 and Pin1. The chicken Par-4 and ATF3 genes were cloned and expressed to confirm co-localisation with Meq in the cell nucleus while further biochemical investigations for each interaction were carried out by co-immunoprecipitation. The Par-4 and ATF3 proteins have been shown to play a variety of key roles in cellular mechanisms such as apoptosis, cell cycle regulation and transformation but we failed to see expression of these proteins in either normal or transformed lymphocytes. However, Par-4 and ATF3 are expressed in the feather follicle epithelium of infected birds providing the potential for a role during lytic infection in the skin. It is clear that more work is required in order to explore this hypothesis further but this thesis describes a number of novel interactions made by Meq and in doing so we have contributed to the greater understanding of Marek’s disease virology.
Issue Date: 2011
Date Awarded: Jul-2012
URI: http://hdl.handle.net/10044/1/9861
DOI: https://doi.org/10.25560/9861
Supervisor: Baigent, Susan
Nair, Venugopal
Allday, Martin
Sponsor/Funder: Biotechnology and Biological Sciences Research Council (Great Britain)
Department: Medicine
Publisher: Imperial College London
Qualification Level: Doctoral
Qualification Name: Doctor of Philosophy (PhD)
Appears in Collections:Medicine PhD theses



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