Scott Holley, PhD
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Professor of Molecular, Cellular and Developmental Biology
Biography
I am Professor and Chair of the Department of Molecular, Cellular and Developmental Biology. My doctoral research at the University of Chicago with Chip Ferguson demonstrated the conservation of dorsal-ventral patterning mechanisms between insects and vertebrates, identified noggin as a BMP inhibitor and originated concept of facilitated morphogen diffusion. I was a Damon Runyon Cancer Research Foundation Postdoctoral Fellow with Nobel Laureate Christiane Nüsslein-Volhard at the Max Planck Institute for Developmental Biology in Tübingen, Germany. As a postdoc, I discovered the zebrafish segmentation clock, a genetic mechanism that leads to vertebral defects such as scoliosis when perturbed in humans. My lab studies the systems developmental biology, biophysics and biomechanics of vertebral column development in zebrafish. We combine in vivo single molecule biophysics, embryology, genetics, live imaging and systems level data analysis and computer modeling to study pattern formation and morphogenesis. We discovered roles for regulated tissue fluidity, self-organized ECM assembly and ECM-mediated inter-tissue adhesion in early spinal column development. My lab’s research has been supported by grants from the NIH, NSF, the American Cancer Society and the March of Dimes.
Education & Training
- PhD
- University of Chicago
- Postdoctoral Fellow
- Max Planck Institut für Entwicklungsbiologie, Tübingen, Germany
Research
Links & Media
Media
Figure 1[4]
Figure 1. To the left is a photograph of a live zebrafish embryo during the first day of development. Somites are the repeated structures that give rise to the vertebral column and skeletal muscle. New somites are created in the tailbud, which is also the leading edge of the extending trunk and tail. The schematic to the right summarizes differences in the flow of migrating cells in the blue, green and cyan regions of the tailbud.Figure 2
Figure 2. Cell movement within the tailbud was imaged, cells were tracked and average cell velocities over a 10 micron radius were calculated in 3D and projected onto a 2-D surface. The warmer colors indicate regions of higher cell velocities. The arrows indicate 2-D projection of the averaged 3-D velocity vectors.Triple.tif (RGB)
Figure 3. High-resolution fluorescent in situ hybridization of the oscillating expression of two segmentation clock genes her1 (green) and deltaC (red). Nuclei are blue. These stripes of gene expression sweep though the tissue in a reiterated, wave-like fashion from posterior (right) to anterior (left). This striped pattern created by the “segmentation clock†presages the segmental pattern of morphological somites and, ultimately, the vertebral column.
News
- February 03, 2016
Research in the news: Straight spines depend upon sawtooth protein pattern
- April 15, 2005
Lessons from the depths
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Locations
Yale Science Building
Academic Office
Kline Biology Tower
Lab