Date of Award:

5-2024

Document Type:

Dissertation

Degree Name:

Doctor of Philosophy (PhD)

Department:

Chemistry and Biochemistry

Committee Chair(s)

Sean J. Johnson

Committee

Sean J. Johnson

Committee

Joan Hevel

Committee

Ryan N. Jackson

Committee

Nicholas E. Dickenson

Committee

Abby D. Benninghoff

Abstract

RNA, known as ribonucleic acid, is indispensable in every facet of life. RNAs participate in key processes such as transcription, translation, post-translational modification, and cell signaling. Remarkably, certain RNAs exhibit catalytic activity. Given RNA's diverse roles, it is unsurprising that defects in RNA metabolism can cause cancer and neurodegenerative diseases. Therefore, cells employ various mechanisms to regulate and manage their RNA population.

In the nucleus, the RNA exosome is the major 3'→5' machinery that processes and degrades RNA. Various diseases have been associated with mutations in RNA exosome subunits. Some of these diseases are associated with impaired interactions with the RNA exosome cofactor, Mtr4. Mtr4 is an essential RNA helicase that serves as a bridge between upstream RNA targeting and downstream RNA decay. To better understand the role Mtr4 plays in these processes and diseases, we investigate Mtr4 by biochemically characterizing the conserved C-terminus and its interactions with the RNA exosome, developing a FRET-based system to monitor protein dynamics, and exploring paralogs from the model system Arabidopsis thaliana.

Checksum

1bdcbc558450f65a045d3d69941ec37d

Available for download on Tuesday, May 01, 2029

Included in

Biochemistry Commons

Share

COinS