Date of Award
2018
Document Type
Dissertation/Thesis
Submission Date
October 2026
Thesis/Dissertation Advisor [Chair]
Moore, Jon
Abstract
The nuclear receptors REV-ERBα (NR1D1) and REV-ERBβ (NR1D2) play a major role in the regulation of the circadian rhythm. They work together with the nuclear receptor RORγt in gene activation and repression at RORE sites. These sites are found in TH17 cells that are known for their production of proinflammatory cytokines causing chronic inflammation, which is a prominent feature in many autoimmune diseases. In this study, the REVERBα/REVERBβ binding complex was examined for its role in the expression of a known target gene, BMAL1. Furthermore, additional investigations were conducted to elucidate the roles that REVERBα and REVERBβ have in the immune system and to identify protein binding partners in the REVERB complex.
Recommended Citation
Pelletier, Oliver, "A STUDY TO IDENTIFY THE TRANSCRIPTIONAL BINDING PARTNERS FOR THE NUCLEAR RECEPTORS REV-ERB α AND REV-ERB β IN THE REGULATION OF TH17 CELL DEVELOPMENT" (2018). Harriet L Wilkes Honors College Theses 2010 - 2019. 366.
https://digitalcommons.fau.edu/etd_honors_2/366
Extent
42 p.
Identifier
FAUHT00039
Comments
Includes bibliography.