Keywords
Chlamydia trachomatis; Hippo pathway; Translocated Actin Recruiting Phosphoprotein; N-Tarp; Drosophila melanogaster; Epistasis
Abstract
Chlamydia trachomatis causes the most prevalent bacterial sexually transmitted infection in the world, affecting millions of people annually. Chlamydia secretes protein effectors to assist in infection, yet many of these effectors are uncharacterized. One effector, the translocated actin-recruiting phosphoprotein (Tarp), is important for efficient host cell entry. Tarp has a well-characterized C-terminus, but its N-terminus remains relatively uncharacterized. Recent studies into the N-terminus of Tarp reveal that it interacts with the Hippo signaling pathway, which regulates cell proliferation and death. Interestingly, Chlamydial infection delay host cell death, allowing the pathogen time to complete its intracellular replication cycle. Thus, the interaction between this effector and the Hippo signaling pathway warrants further investigation. Determining the location of this interaction can help establish a molecular mechanism by which the N-terminus of Tarp (N-Tarp) interacts with the Hippo signaling pathway. This thesis investigates where N-Tarp interacts with the Hippo signaling pathway by testing epistatic interactions. To test for these epistatic interactions, we used Drosophila melanogaster as a model organism. Expression of N-Tarp in Drosophila wings results in tissue overgrowth while overexpression of Hippo pathway core signaling proteins results in a reduction or complete absence of wings. By co-expressing N-Tarp and Hippo pathway components, we were able to observe whether N-Tarp was able to rescue the wing-reduction phenotypes observed with Hippo expression alone. The results can point to where the interaction takes place along the Hippo pathway. We found mixed results, with the strongest evidence consistent with N-Tarp interacting downstream of the core kinase cascade of the signaling pathway. Given the recently discovered role of N-Tarp in contributing to overgrown wings, our study extends these findings and characterizes the effect of Hippo pathway expression and coexpression with N-Tarp.
Thesis Completion Year
2026
Thesis Completion Semester
Spring
Thesis Chair
Aranjuez, George
College
College of Medicine
Department
Burnett School of Biomedical Sciences
Thesis Discipline
Burnett School of Biomedical Sciences
Language
English
Access Status
Campus Access
Length of Campus Access
5 years
Campus Location
Orlando (Main) Campus
STARS Citation
Patel, Dev S., "Determining The Location Of Interaction Between The Hippo Signaling Pathway And The Chlamydia Trachomatis Tarp N-Terminal Region Using Drosophila Melanogaster As An In Vivo Model" (2026). Honors Undergraduate Theses. 512.
https://stars.library.ucf.edu/hut2024/512
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