How much DNA is too much?
Name
barker-julietb-phd-biology-2024-thesis.pdf
Description
Thesis PDF
Size
13.1 MB
Format
Adobe PDF
Checksum (MD5)
e9bb2e8e8e5fec3194a4785ebf893519
Author(s)
Barker, Juliet C.
Advisor(s)
Bell, Stephen
Date Issued
May 2024
Publisher
Massachusetts Institute of Technology
Abstract
Cells exhibit great diversity in the amount of DNA that they contain, and whole genome duplication events explain much of this diversity. But, whole genome duplication typically obstructs the proliferation of cells in which it occurs. How cells survive and proliferate after DNA content is increased is unknown, and fundamental to understanding the evolutionary success of organisms and cancers. I address this unknown by identifying determinants of cell survival immediately upon whole genome duplication, using budding yeast as a model. I identify the range in number of whole genome duplications (ploidies) that cells can survive. I demonstrate that cell growth accompanies increased ploidy across this range, and that physical determinants alleviating and exacerbating cell surface stress increase and decrease the limit to viable ploidy, respectively. I also identify gene expression changes characteristic of whole genome duplication, immediately as it occurs. In part because recapitulating physiologic effects implied by this signature does not impact the range of ploidies with which cells survive, I propose that ploidy is inherently limited by the impacts of growth in size, which accompany whole genome duplication, to the integrity of the cell surface.
MIT Department
Massachusetts Institute of Technology. Department of Biology
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