Date of Award

Spring 2026

Language

English

Embargo Period

5-10-2028

Document Type

Master's Thesis

Degree Name

Master of Science (MS)

College/School/Department

Department of Biological Sciences

Program

Biology

First Advisor

Gabrielle Fuchs

Committee Members

Cara Pager, Hannah Shorrock, Thomas Begley

Keywords

programmed ribosomal frameshifting, noncanonical initiation

Subject Categories

Biology | Laboratory and Basic Science Research | Virology

Abstract

Programmed ribosomal frameshifting (PRF) is a process where the ribosome is stimulated by the RNA sequence to change into a different reading frame, resulting in a protein product with an alternative C-terminus. Many viruses and several cellular RNAs use PRF to express variant proteins through bypassing a stop codon. Typically, frameshifting stimulatory elements (FSEs) in cellular RNAs trigger +1 frameshifting, while those in viral RNAs cause -1 frameshifting. Because PRF is promoted by pauses in translation that increase the likelihood of tRNA realignment, we hypothesized that the rate of translation initiation may impact frameshifting efficiency. To test this hypothesis, we assayed the frameshifting efficiency of a firefly luciferase-SARS-CoV-2 FSE-NanoLuciferase reporter under different modes of initiation and in the presence or absence of cellular stress. Our results show this reporter system can be used successfully to examine this relationship, and that initiation mode may impact stop codon recognition and frameshifting efficiency.

License

This work is licensed under the University at Albany Standard Author Agreement.

Available for download on Wednesday, May 10, 2028

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