Functional Consequences of Rna Exosome Complex Alteration By Conformational Changes and Cofactor Binding

<p>The RNA exosome is an essential 3’-5 ribonuclease that processes or degrades a variety of RNA species in eukaryotes. It is composed of nine structural cores and one catalytic subunit, Rrp44. Structural studies captured two different conformations of Rrp44, Rrp44^ch (channel) and Rrp44^da (direct-access). The Rrp44^ch appears to recruit RNA substrates from the central channel formed by the core subunits, while the substrate is directly recruited to Rrp44^da bypassing the central channel. Although in vivo function of the Rrp44^ch-exosome is extensively studied, the function or even the presence of the Rrp44^da-exosome in cell has not been tested. In this study, I show the first i<em>n vivo</em> evidence that the Rrp44^da is important for the RNA exosome function. I also found that the Rrp44^da and Rrp44^ch have distinct substrates, indicating that the RNA exosome alternates its conformation to exert specific functions. Furthermore, RNA sequencing analysis suggests that Rrp44^ch-exosome indirectly regulates expression of genes encoding ribosomal proteins.</p> <p>The substrate specificity of the RNA exosome is partly determined by its cofactors that bind substrates. Rrp6 is a ribonuclease that interacts with the RNA exosome in the nucleus. It functions not only as a nuclease but also as an adaptor protein that bridges the RNA exosome to other cofactors such as an RNA helicase, Mtr4. In this study, I found that Rrp6 and Mtr4 function beyond known biochemical and structural interactions. Mtr4 seems to interact with the RNA exosome independent of the Rrp6 N- terminus. In addition, the C-terminal domain of Rrp6 has functions other than the exosome interaction. Moreover, another exosome cofactor, Mpp6, appears to mediate the interaction of the RNA exosome with other nuclear cofactors, and this function is redundant with Rrp6.</p> <p>This work demonstrates that there are two different RNA exosome conformations present <em>in vivo</em>, and they have specific functions. Additionally, I show that there are multiple dynamic interactions among the RNA exosome with its cofactors, which ensures proper processing or degradation of transcripts.</p>

Name thesis:degree_name

Doctor of Philosophy (PhD)

Level thesis:degree_level

Dissertation (PhD)

Year dc:date.available

2017

Authors dc:creator

• Han, Jaeil
• <p>0000-0003-3115-4566</p>

Contributors dc:contributor

• Ambro van Hoof
• Swathi Arur
• Theresa M. Koehler

• RNA exosome
• Rrp6
• RNA decay
• Mpp6
• RNA processing
• Dis3
• Rrp44
• Genetics
• Molecular Genetics
• Other Microbiology

Repository record dc:identifier

https://digitalcommons.library.tmc.edu/utgsbs_dissertations/791

OAI identifier oai:identifier

oai:digitalcommons.library.tmc.edu:utgsbs_dissertations-1833