A novel role of the vaccinia virus mRNA capping enzyme in determining virus host range

dc.contributor.authorVarga, Jessie
dc.contributor.examiningcommitteeBooth, Stephanie (Medical Microbiology and Infectious Diseases) Kung, Sam (Immunology)en_US
dc.contributor.supervisorCao, Jingxin (Medical Microbiology and Infectious Diseases)en_US
dc.date.accessioned2019-01-08T18:38:59Z
dc.date.available2019-01-08T18:38:59Z
dc.date.issued2018-12-20en_US
dc.date.submitted2018-12-20T18:18:15Zen
dc.date.submitted2019-01-08T16:02:42Zen
dc.degree.disciplineMedical Microbiology and Infectious Diseasesen_US
dc.degree.levelMaster of Science (M.Sc.)en_US
dc.description.abstractE3 family proteins are a poxvirus defense gene that have a significant role in host range determination. Their biological function has largely been attributed to the ability of the protein to bind double-stranded RNA. Increasing evidence indicates this mechanism is more complex. For example, the ortholog, SPPV034, is unable to rescue replication of a recombinant virus even though it retains the ability to bind dsRNA. The Vaccinia virus capping enzyme (the D1-D12 heterodimer) is a cofactor for E3 protein in determining host range. A D1-G801S mutation rescued replication of the SPPV034 recombinant virus and inhibited activation of host responses. A D12-S131N partially rescue replication, but could not fully antagonize host responses. These results indicate that E3 proteins operate on a threshold mechanism determined by intrinsic properties. The D1-D12 heterodimer mutations altered the quantity of dsRNA produced during infections so that the upper limit of the SPPV034 protein was not reached.en_US
dc.description.noteFebruary 2019en_US
dc.identifier.urihttp://hdl.handle.net/1993/33660
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.subjectVaccinia Virusen_US
dc.titleA novel role of the vaccinia virus mRNA capping enzyme in determining virus host rangeen_US
dc.typemaster thesisen_US
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