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Assistant Professor, Molecular Genetics and Cell
Biology,
Committees on Genetics, Genomics and Systems Biology and on Developmental Biology
BS Chemistry, University of Oregon, 1996
PhD Genetics, University of California, San Francisco, 2003
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During development, discrete organs
and entire body plans emerge from the coordinate actions of individual
cells. These complex morphogenetic events require dynamic regulation
of cell shape, polarity and adhesion across cell populations. Our
lab seeks to understand how these cellular behaviors are orchestrated
to produce an organ’s final shape.
To address this question we are investigating
the morphogenetic mechanisms that create the elliptical shape of
the Drosophila egg. Each fly egg arises from a multi-cellular
follicle, in which the germ cells are surrounded by a somatic epithelium.
Initially spherical, follicles lengthen dramatically along their
A-P axes during oogenesis. We have identified a large collection
of mutations that disrupt follicle elongation, thus providing an
unprecedented opportunity to dissect the molecular mechanisms governing
this poorly understood process. Two questions in which we are particularly
interested are outlined below.
How is planar polarity
established in the follicular epithelium?
Follicle elongation depends on the precise, planar arrangement of
cytoskeletal and extracellular matrix molecules at the basal surface
of the follicular epithelium. Interestingly, this example of planar
polarity does not depend on the well studied Frizzled-PCP signaling
pathway, suggesting that an unconventional regulatory mechanism
operates in this tissue. We are using genetic, cell biological and
biochemical approaches to investigate the molecular mechanisms controlling
this novel planar polarity system.
What are the cellular
behaviors that drive follicle elongation?
Planar polarity is used to coordinate individual cellular behaviors
within the epithelium during follicle elongation, but the nature
of these cellular behaviors is mysterious. We are employing dynamic
live imaging techniques, in both wild-type and mutant contexts,
to better understand the polarized cell behaviors that drive this
morphogenesis.
Horne-Badovinac, S. and Bilder, D.
(2008). Dynein regulates epithelial polarity and the apical localization
of stardust A mRNA. PLoS Genetics, 4(1), 40-51. (PubMed)
Horne-Badovinac, S. and Bilder, D.
(2005). Mass Transit: epithelial morphogenesis in the Drosophila
egg chamber. Developmental Dynamics, 232(3), 559-574. (PubMed)
Horne-Badovinac, S., Rebagliati,
M. and Stainier, D.Y. (2003). A cellular framework for gut looping
morphogenesis in zebrafish. Science, 302(5645), 662-665. (PubMed)
Horne-Badovinac, S., Lin, D., Waldron,
S., Schwarz, M., Mbamalu, G., Pawson, T., Jan, Y.N., Stainier, D.Y.R.,
Abdelilah-Seyfried, S. (2001). Positional cloning of heart and soul
reveals multiple roles for PKC-gamma in zebrafish organogenesis.
Current Biology 11, 1492-1502. (PubMed)
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