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University of Illinois at Urbana-Champaign

The nidogen-domain protein DEX-1 is necessary for the Caenorhabditis elegans dauer morphology and behavior

Abstract

dc:description

The ability to modify a given phenotype to adapt to the external environment (i.e. phenotypic plasticity) is a critical component of an organism’s ability to survive unfavorable conditions. The free-living nematode, Caenorhabditis elegans is an excellent example of phenotypic plasticity. When exposed to unfavorable conditions, C. elegans halts reproductive development and enters an alternative developmental stage called dauer. Dauer larvae undergo extensive tissue remodeling, including changes to the outer cuticle, muscle, and nervous system. Although several morphological and behavioral traits of the dauer larvae have been described, the molecular mechanisms underlying dauer-specific tissue remodeling have remained poorly understood. This work provides evidence that the nidogen domain-containing protein DEX-1 facilitates the stage-specific tissue remodeling observed during dauer morphogenesis. DEX-1 was previously shown to function as a secreted extracellular matrix protein that regulates sensory dendrite formation during embryogenesis. However, we found an alternative developmental role for DEX-1. Specifically, we show that DEX-1 is also required for remodeling of the stem-cell like hypodermal seam cells and formation of the cuticular lateral alae. Further, we found that DEX-1 is necessary for proper dauer mobility, and may function as a component of the neuromuscular system to facilitate dauer locomotion behaviors. We show that dex-1 is secreted from the seam cells, but functions locally in a cell-autonomous manner to facilitate dauer morphogenesis. dex-1 expression during dauer is also regulated through DAF-16/FOXO-mediated transcriptional activation. Finally, we show that dex-1 genetically interacts with a family of zona pellucida-domain genes to regulate seam cell remodeling and alae formation. Taken together, this work shows that DEX-1 is an extracellular matrix component that plays a critical role in C. elegans tissue plasticity during dauer formation.

Degree

thesis:*
Name thesis:degree_name
Ph.D.
Level thesis:degree_level
Dissertation
Discipline thesis:degree_discipline
Neuroscience
Grantor
University of Illinois at Urbana-Champaign
Year dc:date
2020

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Flatt, Kristen M.
Contributors dc:contributor
  • Schroeder, Nathan
  • Juraska, Janice
  • Brieher, William
  • Vidal-Gadea, Adres

Subjects

dc:subject × 6

Rights

dc:rights
Statement dc:rights
  • Copyright 2019 Kristen Flatt
Language dc:language
en

Identifiers

dc:identifier.*
Handle dc:identifier
http://hdl.handle.net/2142/106193
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/106193

Chain of custody

source
Harvested from
University of Illinois - Urbana-Champaign
Base URL
www.ideals.illinois.edu/oai-pmh
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Flatt, Kristen M.. The nidogen-domain protein DEX-1 is necessary for the Caenorhabditis elegans dauer morphology and behavior. Dissertation thesis, University of Illinois at Urbana-Champaign, 2020. http://hdl.handle.net/2142/106193