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The Role and Molecular Mechanisms of Rex1 in Pluripotent Stem Cells

Pluripotent stem cells (PSCs) are unique in their capability to self-renew and
differentiate into cell types of all three embryonic germ layers. Since their discovery, PSCs
have become an indispensable tool for modeling development, disease onset/progression,
and drug discovery. The pluripotent state is known to be regulated by a core network of
transcription factors including Oct4, Sox2, and Nanog. However, the roles of other
contributing transcription factors remain understudied. Our research focused on defining
the roles and molecular mechanisms of Rex1, a zinc finger transcription factor whose
expression is strongly correlated with the pluripotent state. Attempts by our lab to elucidate
the role of Rex1 in embryonic stem cells (ESCs) revealed the presence of two smaller
protein products that result from the initiation of translation at downstream start codons
within the REX1 open reading frame. We hypothesized that the full-length Rex1 protein
and its shorter alternative translation isoforms were acting to regulate the expression of
lineage-determining genes in PSCs. To evaluate this hypothesis, we generated mouse
embryonic stem cell (mESC) lines expressing FLAG-tagged versions of the full-length
Rex1 protein, and its isoforms, from the endogenous locus. Through the use of these lines,
we demonstrated the formation of multiple Rex1 isoforms by alternative translation, a novel
observation that has yet to be reported. Furthermore, our results indicate that Rex1 is a
negative regulator of differentiation-related genes and endogenous retroviral elements,
suggesting Rex1 is acting to maintain the tightly regulated transcriptional network of
pluripotency, while also maintaining genomic integrity through the repression of repetitive
elements. / Thesis / Master of Science (MSc)

Identiferoai:union.ndltd.org:mcmaster.ca/oai:macsphere.mcmaster.ca:11375/22339
Date January 2017
CreatorsHrenczuk, Amanda
ContributorsDraper, Jonathan, Biochemistry and Biomedical Sciences
Source SetsMcMaster University
LanguageEnglish
Detected LanguageEnglish
TypeThesis

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