Files in this item

FilesDescriptionFormat

application/pdf

application/pdfANDROWSKI-DISSERTATION-2020.pdf (5MB)Restricted to U of Illinois
(no description provided)PDF

Description

Title:Stress-induced remodeling of the caenorhabditis elegans dauer
Author(s):Androwski, Rebecca Joann
Director of Research:Schroeder, Nathan E
Doctoral Committee Chair(s):Schroeder, Nathan E
Doctoral Committee Member(s):Gillette, Martha; Gillette, Rhanor; Vidal-Gadea, Andres
Department / Program:Neuroscience Program
Discipline:Neuroscience
Degree Granting Institution:University of Illinois at Urbana-Champaign
Degree:Ph.D.
Genre:Dissertation
Subject(s):C. elegans
dendrite
stress
TOR
Insulin signaling
Abstract:Dendrite morphology is critical to the proper function of the nervous system. Stress-induced changes to the dendritic architecture of neurons has been demonstrated in numerous mammalian and invertebrate systems; however, stress-induced remodeling of dendrites varies among neuron types. During the stress-induced dauer stage of Caenorhabditis elegans, the IL2 neurons arborize to cover the anterior body wall. In contrast, the FLP neurons arborize to cover an identical receptive field in favorable conditions. How coordinated branching is established between these two neuronal subtypes is unknown. Additionally, the molecular mechanisms that underlie stress-induced dendrite morphology are poorly understood. Therefore, the goal of my dissertation is to identify effectors of IL2 dendritic morphology and determine how branching is differentially regulated between IL2 and FLP neurons. In Chapter 2, I describe the neuronal architecture of the FLPs, identify a neighborhood effect on IL2 and FLP dendrites, and characterize new alleles of branching regulators kpc-1 and dma-1. Chapter 3 shows that both the IL2s and FLPs use an identical downstream effector complex comprising of the L1CAM homolog SAX-7 to control branching. Chapter 4 compares regulation of this complex between stress-induced IL2 branching and FLP branching. Here I find a previously unknown genotype by environment interaction within the UPR, demonstrating temperature-dependent regulation of neuronal, pharyngeal, and cuticular remodeling in the dauer. In Chapter 5, I show that several aspects of the dauer formation pathway are necessary for the neuron to remodel, including the FOXO transcription factor/DAF-16, phosphatase PTEN/DAF-18 and Cytochrome P450/DAF-9. Finally, we find that the TOR associated protein, RAPTOR/DAF-15 regulates mutually exclusive branching of the IL2 and FLP dendrites. Together, our results shed light on molecular processes that regulate stress-mediated remodeling of dendrites across neuron classes.
Issue Date:2020-09-28
Type:Thesis
URI:http://hdl.handle.net/2142/109469
Rights Information:Copyright 2020 Rebecca Androwski
Date Available in IDEALS:2021-03-05
Date Deposited:2020-12


This item appears in the following Collection(s)

Item Statistics