Date of Award
Summer 8-20-2023
Degree Type
Thesis
Degree Name
Master of Science (MS)
Department
Biological Science
First Advisor
William Gilliland, PhD
Second Advisor
Joanna Brooke, PhD
Third Advisor
Philip Funk, PhD
Abstract
Organisms can defend against pathogens by significantly increasing the diversity of their progeny, so that some progeny are more likely to survive infection. This led to the prediction that infection should cause an increase in recombination rates which was seen in a previous study. However, the mechanism that regulates recombination rates in response to infection is not understood and in that study they did not provide a mechanism for how that can occur. In an RNAi screen, our lab found the gene mustard (mtd) is required for normal recombination rates. This gene was previously shown to be part of the Immune Deficiency Pathway. When mtd was knocked down by RNAi, we saw an ~95% reduction in recombination rates. This suggests that the IMD pathway may be part of the mechanism that modulates recombination rates in response to bacterial infection. We tested this by measuring if the recombination rate changes caused by P. rettgeri infection depends on mtd function. We found that infecting female flies with the bacteria did not have any change in recombination rates between the control groups and the experimental groups.
Recommended Citation
Mashburn, Sarah, "Characterization of the Immune Deficiency Pathway during female meiosis in Drosophila melanogaster" (2023). College of Science and Health Theses and Dissertations. 502.
https://via.library.depaul.edu/csh_etd/502
SLP Collection
no