Date of Graduation

Summer 2026

Degree

Master of Science in Biomedical Sciences

Department

School of Heath Sciences

Committee Chair

Randi Ulbricht

Abstract

Adenosine-to-inosine (A-to-I) RNA editing is a post-transcriptional mechanism mediated by ADAR enzymes that can alter RNA sequence, protein function, and gene regulation. Because ADAR1 is upregulated during inflammation and plays a critical role in innate immunity, previous studies investigated the effects of acute inflammation on RNA editing in male and female mice. Lipopolysaccharide (LPS) was used to induce inflammation, and RNA editing levels were examined in the heart, brain, and skeletal muscle. While editing levels in the heart and brain remained unchanged, skeletal muscle exhibited tissue- and sex-specific differences in editing. In this thesis, LPS treatment affected selective editing, increasing editing of RPA1 in females and decreasing RPA1 editing in males, indicating that inflammation can influence RNA editing in a sex-dependent manner. In contrast, hyperediting of the ADAR1 target AZIN1 was not significantly affected by inflammation. Attempts to measure ADAR1 protein expression were unsuccessful, due to sample age and/or antibody limitations. Overall, these findings demonstrate that the effects of acute inflammation on RNA editing are both tissue- and sex-specific, highlighting the complex interactions between immune activation, RNA processing, and biological sex.

Keywords

MDA5, ADAR1, RIG-I, Innate Immunity, Sex, RNA, adenosine deaminase acting on RNA, retinoic acid-inducible gene I, melanoma differentiation-associated protein 5, RNA editing

Subject Categories

Biology | Cell Biology | Immunity

Copyright

© Skyler LEE

Open Access

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