 
Assistant Professor
PO Box 980614
Richmond, VA 23298-0614
Email: kdbaker@vcu.edu
Telephone: 804-628-4498
Education
- B.A. , Baylor University
- PhD, University of Texas Southwestern Medical Center, 2002.
Post-Doc University of Utah School of Medicine
The role of nuclear receptors in Drosophila metabolism and
development.
Research: The role of nuclear receptors in Drosophila metabolism and
development.
Nuclear receptors are a superfamily of highly
conserved transcription factors that bind small
lipophilic compounds such as fatty acids, steroids, and
bile acids. Upon binding to these ligands, nuclear
receptors facilitate expression of genes involved in
diverse processes, including development, maturation,
reproduction, and metabolic homeostasis. Our long-term
goal is to elucidate the cellular and organism-wide
role(s) of nuclear receptors and their partner proteins.
Accordingly, we use the fruit fly,
/Drosophila
melanogaster/, as a
model organism to delineate fundamental aspects of
nuclear receptor-mediated transcription pathways under
varying developmental and environmental conditions. Our
current studies focus on the transcriptional regulation
of glycolytic pathways by the estrogen receptor-related
receptor (ERR). Mounting evidence suggests that ERR
significantly impacts nearly every aspect of
carbohydrate metabolism. Moreover, we have recently
discovered a direct link with ERR to the
hypoxia-inducible factor-1a (HIF-1)
HIF-1 sits at the top of a transcriptional hierarchy
that mediates a broad cellular adaptation program in
response to oxygen deprivation. It has been estimated
that 2-5% of all genes change their expression profile
in a HIF-dependent manner when subjected to hypoxia;
these changes often have a profound effect on cellular
‘character’ and decision-making. Among the processes
most affected are the stimulation angiogenesis,
erythropoiesis, and glycolysis. Importantly, ectopic and
unregulated activity of the HIF-1 pathway occurs in many
forms of human cancers, making HIF-1-mediated
transcription an attractive target for cancer therapy.
ERR’s unexpected role in the hypoxic response provides a
new avenue by which the HIF-1 pathway may be targeted.
In particular, we are interested in understanding the
circumstances that dictate ERR collaboration with HIF-1
and how this pairing influences energy expenditure
decisions.
Publications
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