Epitope tags are not created equal: disruption of cellular function of a translation factor by a short viral tag

dc.access.optionRestricted Campus Access Only
dc.contributor.advisorKeiper, Brett D
dc.contributor.authorBarker, Brooke K
dc.contributor.departmentBiochemistry and Molecular Bio
dc.date.accessioned2025-02-20T20:39:38Z
dc.date.created2024-12
dc.date.issued2024-12-04
dc.date.submittedDecember 2024
dc.date.updated2025-02-06T14:50:40Z
dc.degree.departmentBiochemistry and Molecular Bio
dc.degree.disciplineBiology
dc.degree.grantorEast Carolina University
dc.degree.levelUndergraduate
dc.degree.nameBS
dc.description.abstractCellular identity and fate are determined by the proteins synthesized. Initiation of mRNA translation requires an important translation factor eIF4G (ifg-1 in C elegans). Embryos use mRNA translation for spatial and temporal regulation of protein synthesis. Using CRISPR engineering, we added in-frame epitope and fluorescent tags (V5, Myc, Flag, GFP and mCherry) to IFG-1. Tagged forms containing the V5 epitope caused embryonic arrest. Internal disruption of the V5 tag restored viability at 25°C. This study demonstrates that the molecular nature of a small epitope tag is sufficient to disrupt C. elegans embryogenesis.
dc.embargo.lift2025-12-01
dc.embargo.terms2025-12-01
dc.format.mimetypeapplication/pdf
dc.identifier.urihttp://hdl.handle.net/10342/13939
dc.subjectembryogenesis, mRNA translation, protein tags
dc.titleEpitope tags are not created equal: disruption of cellular function of a translation factor by a short viral tag
dc.typeHonors Thesis
dc.type.materialtext

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