Numerous noncoding RNAs (ncRNAs) exist in organisms in all three domains of life. In recent years, there has been an explosion in the discovery of novel ncRNAs and their implications in human disease. These ncRNAs are responsible for a remarkable variety of biological functions, including essential roles in the most fundamental aspects of metabolism. In bacteria, ncRNAs perform a diverse array of regulatory functions in controlling genetic signaling and cellular homeostasis. A number of ncRNA classes with extraordinary structural complexity that are among the largest known bacterial ncRNAs have recently been discovered. Of these, OLE (ornate, large, extremophilic) is a conserved, exceptionally structured RNA class that exists almost exclusively in anaerobic extremophiles, including many species of human gut bacteria, human pathogens and organisms with industrial uses. Previous studies have made significant advances toward determining the biological role of the OLE RNA class. However, the function of OLE RNA remains unknown. Therefore, the overall goal of this proposal is to establish its function using several approaches. Specifically, this will be accomplished by (1) identifying the OLE RNA interaction network with crosslinking and co-purification experiments, (2) investigating the cellular localization of OLE RNAs in response to stress with fluorescence microscopy, and (3) applying bioinformatics and biochemical assays to identify ligands for OLE RNAs. Determining the function of this ncRNA class will undoubtedly have an impact on our knowledge about the capabilities of RNA and fundamental aspects of biology, as well as, have potential health-related applications.

Public Health Relevance

Pathogenic bacteria and microbial communities in the human gut are responsible for numerous human health concerns. The proposed research will investigate the role of a new class of biological molecules unique to bacteria. Results from these studies could lead to the development of novel antimicrobials and diagnostics for disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM116426-02
Application #
9206414
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Barski, Oleg
Project Start
2015-08-01
Project End
2017-07-31
Budget Start
2016-08-01
Budget End
2017-07-31
Support Year
2
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Yale University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
Harris, Kimberly A; Zhou, Zhiyuan; Peters, Michelle L et al. (2018) A second RNA-binding protein is essential for ethanol tolerance provided by the bacterial OLE ribonucleoprotein complex. Proc Natl Acad Sci U S A 115:E6319-E6328
Greenlee, Etienne B; Stav, Shira; Atilho, Ruben M et al. (2018) Challenges of ligand identification for the second wave of orphan riboswitch candidates. RNA Biol 15:377-390
Harris, Kimberly A; Breaker, Ronald R (2018) Large Noncoding RNAs in Bacteria. Microbiol Spectr 6:
Li, Sanshu; Lünse, Christina E; Harris, Kimberly A et al. (2015) Biochemical analysis of hatchet self-cleaving ribozymes. RNA 21:1845-51
Harris, Kimberly A; Lünse, Christina E; Li, Sanshu et al. (2015) Biochemical analysis of pistol self-cleaving ribozymes. RNA 21:1852-8