Undergraduate Honors Theses

Thesis Defended

Spring 2013

Document Type

Thesis

Department

Integrative Physiology

First Advisor

Thomas E. Johnson, Ph.D.

Abstract

In Caenorhabditis elegans expression of the fluorescent reporter (Phsp-16.2::GFP) is driven by transcription of a stress-responsive promoter sequence and has been shown to predict subsequent stress resistance (thermotolerance) and lifespan of individual animals within an isogenic population (Rea et al., 2005). The mechanism behind the predictive nature of this reporter is poorly understood. To better understand how this reporter works, stress-responsive genes were examined to determine if they were required for the ability of the reporter to predict thermotolerance or lifespan. Animals that had low or high expression of the Phsp-16.2::GFP reporter and contained loss-of-function mutations in select stress-responsive genes were tested to determine whether the animals with higher expression of the reporter still had improved thermotolerance or lifespan. The results revealed that none of the tested stress-responsive genes were necessary for the predictive power of the reporter. In some mutants, the reporter maintained its predictive ability even though the overall thermotolerance was greatly reduced. This implies that the predictive ability of the reporter is not linked to the stress resistance (thermotolerance) of the animal, as originally expected.

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