Skip navigation
Please use this identifier to cite or link to this item: http://arks.princeton.edu/ark:/88435/dsp01pk02cd11n
Full metadata record
DC FieldValueLanguage
dc.contributor.advisorGavis, Elizabeth Ren_US
dc.contributor.authorHughes, Kelseyen_US
dc.contributor.otherMolecular Biology Departmenten_US
dc.date.accessioned2015-12-07T19:52:12Z-
dc.date.available2015-12-07T19:52:12Z-
dc.date.issued2015en_US
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/dsp01pk02cd11n-
dc.description.abstractThe coupling of mRNA localization and translational control is an effective means of establishing spatiotemporal control over gene expression. These controls are established through the combined action of cis-acting elements within the transcript, trans-acting factors that bind them, and the factors that are subsequently recruited to the transcript. Together, the full complement of regulatory elements determines where and when the target mRNA will be translated into protein. A powerful model for the study of mRNA localization and translational control is the tight control of nanos (nos) mRNA during early Drosophila development. Translation of nos mRNA must be restricted to the embryo posterior, and defects in nos localization and translational control significantly impact the formation of the anterior-posterior axis. This thesis presents the identification of novel cis-acting elements and trans-acting factors in translational regulation of nos; in particular, elements in the distal nos 3' untranslated region and Igf-II mRNA-binding protein (Imp). Additionally, this thesis describes the analysis of Imp function in post-transcriptional regulation of oskar (osk), another developmentally important mRNA that functions in germ cell formation and acts upstream of nos in anterior-posterior axis development. Together, these newly identified roles for Imp provide a foundation for future studies aimed at gaining further insight into the regulation of nos and osk, how multiple post-transcriptional regulatory mechanisms are layered to regulate a given transcript, and how one protein regulates multiple transcripts.en_US
dc.language.isoenen_US
dc.publisherPrinceton, NJ : Princeton Universityen_US
dc.relation.isformatofThe Mudd Manuscript Library retains one bound copy of each dissertation. Search for these copies in the library's main catalog: http://catalog.princeton.edu/en_US
dc.subject.classificationMolecular biologyen_US
dc.titleNew Roles for Igf-II mRNA-binding Protein During Early Drosophila Developmenten_US
dc.typeAcademic dissertations (Ph.D.)en_US
pu.projectgrantnumber690-2143en_US
Appears in Collections:Molecular Biology

Files in This Item:
File Description SizeFormat 
Hughes_princeton_0181D_11492.pdf46.9 MBAdobe PDFView/Download


Items in Dataspace are protected by copyright, with all rights reserved, unless otherwise indicated.