Author Type

Graduate Student

Date of Award

2023

Document Type

Dissertation

Publication Status

Version of Record

Submission Date

October 2026

Thesis/Dissertation Advisor [Chair]

Murphey, Rodney

Abstract

Proper formation of synapses in the developing nervous system is critical to the expected function and behavior of an adult organism. Neurons must project neurites, in the form of axons or dendrites, to target areas to complete synaptic circuits. The biochemical tool that cells use to interact with the external environment and direct the guidance of developing neurites are guidance receptors. One such guidance receptor that is extensively studied to uncover its roles in developmental disorders and disease is DSCAM (Down-Syndrome Cell Adhesion Molecule). To better understand the role of DSCAM in humans, a fly homolog Dscam1 was extensively characterized in the giant fiber system (GFS) of Drosophila to further explore its roles in axon guidance, synapse formation, and synapse function. The UAS-Gal4 system was used to alter the protein levels of Dscam1 within the giant fiber interneurons (GFs). A UAS-RNAi construct against Dscam1 was used to knockdown translation of all possible isoforms within the GFs. A UAS-Dscam1(TM2) construct was used to overexpress a single isoform of Dscam1 that is specifically trafficked to the axons. Confocal microscopy was used to determine the morphological changes associated with dysregulated Dscam1 levels. Visualization via fluorescent markers was accomplished of both pre- and post-synaptic cells, the GFs and tergotrochanteral motorneurons (TTMns), respectively, and synapse interface was determined as colocalization of the two cells. Additionally, the functional components of the GF-TTMn synapse, both gap-junctions, and presynaptic chemical active zones were tagged via fluorescent antibodies and quantified.

Extent

116 p.

Comments

Includes bibliography.|Dissertation (PhD)--Florida Atlantic University, 2023.|FAU Electronic Theses and Dissertations Collection|Includes bibliography.

Identifier

FA00014364

Format

pdf

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