Theses and Dissertations

ORCID

https://orcid.org/0009-0002-3123-0725

Issuing Body

Mississippi State University

Advisor

Gout, Jean-Francois

Committee Member

Dapper, Amy

Committee Member

Gordon, Donna M.

Committee Member

Perkins, Andy

Date of Degree

12-8-2023

Document Type

Graduate Thesis - Open Access

Major

Computational Biology

Degree Name

Master of Science (M.S.)

College

Office of Academic Affairs

Department

Computational Biology Program

Abstract

tRNA genes are highly transcribed and perform one of the most fundamental cellular functions. Although a universal pattern observed across all three domains of life is that highly transcribed genes tend to evolve slowly, tRNA genes have been shown previously to evolve rapidly. This rapid sequence evolution could result from relaxed selection, increased mutation rate, or a combination of both. Here, we use mutation-accumulation line sequencing data to show that tRNA genes accumulate more mutations than other gene types. Our results indicate that this elevated mutation rate is a consequence of both elevated transcription-associated mutagenesis and a lack of transcription-coupled repair in tRNA genes. We also identify the gene MSH2 as being involved in transcription-coupled repair.

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