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dc.contributor.advisorPeculis, Brenda A. (Brenda Ann), 1964-eng
dc.contributor.authorTaylor-Holou, Melissa J., 1983-eng
dc.date.issued2009eng
dc.date.submitted2009 Springeng
dc.descriptionTitle from PDF of title page (University of Missouri--Columbia, viewed on Sept 10, 2010).eng
dc.descriptionThe entire thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file; a non-technical public abstract appears in the public.pdf file.eng
dc.descriptionDissertation advisor: Dr. Brenda Peculis.eng
dc.descriptionVita.eng
dc.descriptionIncludes bibliographical references.eng
dc.descriptionPh. D. University of Missouri--Columbia 2009.eng
dc.descriptionDissertations, Academic -- University of Missouri--Columbia -- Biochemistry (Agriculture)eng
dc.description.abstractNudt16, previously called X29, is known to be a metal-dependent decapping enzyme expressed in mammals and Xenopus . Nudt16 has been proposed to be the catalytic component of a previously unknown nuclear RNA degradation pathway that degrades nuclear-limited RNAs. However, nothing was known about the function of the protein in other species. This work proposes to examine whether the sequence and, more importantly, the RNA decapping function of the Nudt16 protein is conserved across evolution. The hypothesis tested here is that if the protein and decapping function are conserved then the proposed in vivo role of a nuclear pathway for RNA degradation is more likely to be true. The experiments demonstrate that the sequence of the Nudt16 protein is evolutionarily conserved across metazoans. Additionally, there is evidence for a gene duplication that occurred at the level of tetrapods resulting in a cytoplasmic protein lacking RNA decapping function. Functional analysis of putative orthologs of Nudt16protein from several divergent organisms demonstrated that the ability to act as an RNA decapping protein is well conserved. More complete characterization of the Nudt16 protein from Xenopus as well we several of the other organisms demonstrated that the protein functions as homodimer with up to two RNA binding sites that may act independently of one another. While metal is a required co-factor, characterization of additional orthologs demonstrated that there is broad RNA substrate specificity for RNA decapping in the presence of both Mg⁺² and Mn⁺². Identification of putative in vivo interacting partners of Nudt16 was performed using co-immunoprecipitations. Three proteins were identified but still need to be verified. Collectively, these data demonstrate that Nudt16 is conserved both in sequence and in vitro function across evolution and support the existence of a nuclear RNA degradation pathway for nuclear-limited RNAs in Metazoans.eng
dc.format.extentxi, 237 pageseng
dc.identifier.oclc695114986eng
dc.identifier.urihttps://hdl.handle.net/10355/9560
dc.identifier.urihttps://doi.org/10.32469/10355/9560eng
dc.languageEnglisheng
dc.publisherUniversity of Missouri--Columbiaeng
dc.relation.ispartofcollectionUniversity of Missouri--Columbia. Graduate School. Theses and Dissertationseng
dc.source.originalSubmitted by University of Missouri--Columbia Graduate School.eng
dc.subject.lcshNucleotide sequenceeng
dc.subject.lcshMetazoaeng
dc.subject.lcshXenopuseng
dc.subject.lcshRNA -- Synthesiseng
dc.titleIn vitro characterization of Nudt16 orthologs by sequence and function provide evidence supporting a nuclear RNA degradation pathwayeng
dc.typeThesiseng
thesis.degree.disciplineBiochemistry (Agriculture) (MU)eng
thesis.degree.grantorUniversity of Missouri--Columbiaeng
thesis.degree.levelDoctoraleng
thesis.degree.namePh. D.eng


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