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Recent research
in the Wente laboratory has focused on using yeast and vertebrate
model systems to further understand the
mechanism of nucleocytoplasmic communication. Nuclear trafficking
is essential to proper cell growth and responses to extracellular signals
during cell cycle and developmental switches.
Trainees in Dr. Wente’s
laboratory have made recent breakthroughs in the understanding the
mechanisms of assembly, translocation through, and regulation of nuclear
pore complexes (NPCs). NPCs embedded in the nuclear envelope provide
the only sites for nuclear entry and exit of macromolecules. Her laboratory
has made insights into the basis of transport factor interactions with
the NPC proteins, and revealed information about protein import/export
pathways and steps in the mRNA export mechanism. Lab members
have also discovered a nuclear inositol polyphosphate pathway that
is required for efficient
mRNA export in both yeast and vertebrate cells. This signaling pathway
represents a new frontier for regulating gene expression and cell physiology.
Recent collaborative work
with trainees in the Bruce Appel
laboratory has revealed a role for this inositol
signaling pathway in zebrafish early development. The researchers have
linked proper inositide production to the establishment of left-right
asymmetry
and modulation of intracellular calcium fluxes during embryogenesis.
This research program illustrates how research on basic aspects of
cell biology impact the understanding of developmental biology, and
the synergy that can result from studying multiple developmental model
systems.
For
more information about Dr. Wente visit her Vanderbilt
Faculty Page or her Lab
Website
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