Theses and Dissertations
Date of Award
5-1-2026
Document Type
Thesis
Degree Name
Master of Science (MS)
Department
Biochemistry and Molecular Biology
First Advisor
Megan Keniry
Second Advisor
Robert Gilkerson
Third Advisor
Sue Anne Chew
Abstract
Forkhead box O (Foxo) transcription factors are key regulators of stem cell identity and tumor aggressiveness. Prior work from our group and others demonstrates that Foxo factors maintain stem-like states across diverse biological systems; however, the mechanisms by which Foxo1 suppresses differentiation remain poorly defined.
Using C2C12 myoblasts as a model, we investigated whether Foxo1 preserves stem-like programs through regulation of the nuclear pore protein Nup210. RNA interference was used to generate Foxo1 knockdown cells, followed by qRT-PCR, RNA-sequencing, and fluorescence microscopy. Transcriptomic analysis revealed widespread gene expression changes involving metabolic, mitochondrial, and transcriptional pathways. Notably, Nup210 expression was significantly altered following Foxo1 knockdown, accompanied by distinct changes in nuclear morphology.
These findings support a model in which Foxo1 coordinates transcriptional programs and nuclear architecture to maintain stem-like states, potentially through Nup210, providing insight into conserved mechanisms of stem cell regulation and cancer progression.
Recommended Citation
Rios, S. A. (2026). Investigating the Ability of Foxo1 to Maintain Stem Cells [Master's thesis, The University of Texas Rio Grande Valley]. ScholarWorks @ UTRGV. https://scholarworks.utrgv.edu/etd/1943

Comments
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