Date Approved

8-2021

Document Type

Dissertation

Degree Name

PhD in Cell & Molecular Biology

Department

Cell Biology and Neuroscience

College

Graduate School of Biomedical Sciences

First Advisor

Natalia Shcherbik, PhD

Committee Member 1

Dimitri Pestov, PhD

Committee Member 2

Mikhail Anikin, PhD

Committee Member 3

Randy Strich, PhD

Committee Member 4

Anton Komar, PhD

Subject(s)

Protein Biosynthesis; Saccharomyces cerevisiae; Ribosomes; Eukaryotic Initiation Factors

Disciplines

Cell Biology | Fungi | Laboratory and Basic Science Research | Life Sciences | Medicine and Health Sciences | Molecular Biology | Molecular Genetics

Abstract

Synthesis of proteins, or translation, is a complex biological process requiring the coordinated effort of numerous protein and RNA factors. Central to translation is the ribosome, a complex macromolecular complex consisting of both ribosomal RNA (rRNA) and ribosomal protein (r-protein). Ribosomes are essential and are one of the oldest and most abundant biomolecules across all forms of life. In addition to the ribosome, translation requires messenger RNA (mRNA), transfer-RNA conjugated to an amino acid (aa-tRNA), translation factors, and energy in the form of ATP and GTP. Translation universally occurs in four major stages, initiation, elongation, termination, and recycling, with initiation serving as the key regulatory and rate-limiting step. The goal of this thesis was to investigate key factors regulating this step. First, a cell-free translation system from the budding yeast Saccharomyces cerevisiae was developed, allowing fine-tuned control of mRNA elements such as the 5’ cap structure. This method was used to uncover a previously undescribed cap-independent translation enhancer from the Black Beetle Virus. Secondly, this method was developed further to utilize purified ribosomes to assay the effect of chemical stress on the ribosome and translation efficiency. This method is a powerful alternative to in vivo approaches since ribosomes can be selectively damaged and assayed without risking contamination of other key molecules like tRNA, mRNA, and translation factors.

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