Mechanism of Dopamine 2-like Receptor Signaling in The Blood Brain Barrier that Regulates Male Courtship in Drosophila Melanogaster

dc.contributor.advisorDauwalder, Brigitte
dc.contributor.committeeMemberGunaratne, Preethi H.
dc.contributor.committeeMemberBawa-Khalfe, Tasneem
dc.contributor.committeeMemberBond, Richard A.
dc.creatorGautam, Sumit
dc.date.accessioned2024-01-26T19:32:33Z
dc.date.createdDecember 2023
dc.date.issued2023-12
dc.date.updated2024-01-26T19:32:34Z
dc.description.abstractIn Drosophila melanogaster, courtship behavior and the brain circuits that mediate it are well characterized. Blood Brain Barrier (BBB) is an important part of the brain. It is purely glial in Drosophila and produces sex-specific modulators of male courtship behavior. One of the sex-specific BBB transcripts encodes a dopamine receptor, D2R, a G protein coupled receptor. D2R plays a major role in many central nervous system functions in both invertebrates and vertebrates. In Drosophila, we have previously found that D2R is preferentially expressed in the SPG cells of the adult male BBB and plays an important role in the regulation of male courtship. However, the molecular pathways downstream of D2R that modulate courtship behavior were unknown. D2R is a member of the family of G protein-coupled receptors (GPCRs) that can signal through two transducers: G proteins and β-arrestin. This study aims to characterize the role of G protein or arrestin signaling of D2R in the BBB for proper male courtship. The question was addressed by employing a genetic and a pharmacological approach. Two unique molecular genetic tools were generated by site-directed mutagenesis, a G protein-biased and a β-arrestin-biased version of D2R. These receptor versions, which can preferentially activate either the G protein or the β-arrestin downstream pathways were examined for their ability to rescue the courtship defects of D2R mutants. In a complementary pharmacological approach, well-known synthetic agonists, the G protein-biased agonist, MLS1547 and the β-arrestin-biased agonist, UNC9994 were administered to flies to examine their potential to rescue the courtship defects of D2R hypomorphic flies. The results from the genetic approach demonstrate that arrestin-mediated, but not G protein-mediated, signaling downstream of D2R is essential for normal male courtship. In agreement with this finding, the courtship defect of D2R hypomorphic flies was rescued by the administration of the arrestin-biased agonist, UNC9994. Together, these findings demonstrate that arrestin-mediated signaling through the D2R receptor in the BBB is required for normal male courtship behavior.
dc.description.departmentBiology and Biochemistry, Department of
dc.format.digitalOriginborn digital
dc.format.mimetypeapplication/pdf
dc.identifier.citationPortions of this document appear in: Love, C. R., Gautam, S., Lama, C., Le, N. H., & Dauwalder, B. (2023). The Drosophila dopamine 2-like receptor D2R (Dop2R) is required in the blood brain barrier for male courtship. Genes, Brain and Behavior, 22(1), e12836.
dc.identifier.urihttps://hdl.handle.net/10657/16190
dc.language.isoeng
dc.rightsThe author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. UH Libraries has secured permission to reproduce any and all previously published materials contained in the work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s).
dc.subjectDopamine 2-like receptor, Courtship, Blood brain barrier, Drosophila melanogaster
dc.titleMechanism of Dopamine 2-like Receptor Signaling in The Blood Brain Barrier that Regulates Male Courtship in Drosophila Melanogaster
dc.type.dcmitext
dc.type.genreThesis
dcterms.accessRightsThe full text of this item is not available at this time because the student has placed this item under an embargo for a period of time. The Libraries are not authorized to provide a copy of this work during the embargo period.
local.embargo.lift2025-12-01
local.embargo.terms2025-12-01
thesis.degree.collegeCollege of Natural Sciences and Mathematics
thesis.degree.departmentBiology and Biochemistry, Department of
thesis.degree.disciplineBiochemistry
thesis.degree.grantorUniversity of Houston
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy

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