Use this URL to cite or link to this record in EThOS:
Title: Knots and crosses : the roles of RNA structure and the 3B protein in foot-and-mouth disease virus replication
Author: Ward, Joseph Charles James
Awarding Body: University of Leeds
Current Institution: University of Leeds
Date of Award: 2018
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Thesis embargoed until 01 Mar 2024
Access from Institution:
Foot-and-mouth disease virus (FMDV) is a single stranded RNA virus in the picornavirus family. It is the causative agent of foot-and-mouth disease, globally the most important a�iction of cloven hoofed animals. The FMDV genome has several features that are not found amongst other viruses within the Picornaviridae. These include a large 50 untranslated region (UTR), almost twice the length of that found in enteroviruses, containing highly structured RNA elements unique to FMDV, such as the S-fragment and several tandemly repeated pseudoknots. Unique aspects are also found within the coding region, where FMDV is the only picornavirus reported to contain multiple copies of the 3B gene. The reasons behind possession of these unusual deviations from the dogma of the picornaviral genome is so far unknown and therefore poses an attractive target for further research. The S-fragment is a predicted 360 nucleotide stem-loop at the 50 end of the FMDV genome. The better studied poliovirus (PV) has a well characterised 80 nucleotide clover leaf structure in the equivalent position which is used as a model for potential S-fragment function. In close proximity to the S-fragment are a series of tandemly repeated pseudoknots, these pseudoknots are maintained across all sequenced isolates of FMDV, however, the number of pseudoknots varies between two and four depending on the specifc isolate. As with the S-fragment, no function is yet assigned to these pseudoknots and the reason behind the variation in number remains unknown. Here, biochemical probing of the S-fragment and pseudoknots has been used to confirm the secondary structures of these elements and helped inform mutagenesis experiments to disrupt conformations. Sub-genomic FMDV replicons are used in tandem with infectious virus to help dissect the roles of these elements in distinct areas of the viral lifecycle. Alongside RNA structure in the 50 UTR, this thesis also investigates the nonstructural P3 region and how the 3B protein plays a key role in correct polyprotein processing. The complex dynamics of picornavirus polyprotein processing generates intermediate products which expand the repertoire of functions encoded in the genome. Dissecting these processes is therefore key for understanding the details of virus replication. As the polyprotein of FMDV uniquely includes three tandem functional copies of the 3B primer peptide, the manipulation of P3 cleavage sites is used here to further uncover the roles of the 3B protein in replication. The importance of the C-terminal region of 3B3 for correct polyprotein processing is described as well as the capabilities for 3B proteins to accept C-terminal fusions, providing a novel set of molecular tools and approaches to further analyse the complexities of picornavirus genome replication in the future.
Supervisor: Stonehouse, Nicola J. ; Rowlands, Dave J. Sponsor: BBSRC
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available