Julia Oxford. PH.D (BSU)

Project Information

Name: Julia Oxford. PH.D

Institution: Boise State University

Department: Biological Sciences


Multiplicity of Col11a1 function during development; structure and signaling

Extracellular matrix molecules play determining roles in development of complex structures such as the vertebrate eye and skeleton.  Mutations in genes that encode proteins of the extracellular matrix demonstrate the importance of individual molecular constituents in the case of Stickler and Marshall syndromes in which a mutation in the Col11a1 gene causes both eye and bone manifestations in a given individual.  The proposed work will address the hypothesis that Col11a1 acts to control cellular differentiation by interacting with regulatory signaling pathways.  Alternatively, Col11a1 could act as a signaling molecule itself.  Similarities exist between the phenotypes resulting from mutations in the BMP, Wnt, and PTHrP signaling pathways and mutations in Col11a1.  The experimental approach proposed to address this hypothesis will combine three levels of analysis—a zebrafish model system for the analysis of vertebrate development, analysis of signaling pathways at the cellular level using cell culture, and molecular structure and interaction studies using biochemical and biophysical techniques to investigate molecular mechanisms of complex events during development and differentiation.   The results of these studies will provide a more thorough understanding of the molecular and cellular mechanism of cell-matrix interactions and how such interactions influence signaling events.  Moreover, we anticipate an increased understanding of how single molecules may be used for multiple purposes in a variety of contexts within a vertebrate organism, as well as the fundamental molecular events that are common to multiple unique outcomes during organogenesis.  With an increase in understanding, we anticipate an improved ability to design new diagnostic approaches and therapeutic strategies to address the challenges introduced by mutations that affect eye and skeletal development.

Team Members: 
Julia Thom Oxford, Ph.D., Cheryl Jorcyk, Ph.D., Owen McDougal, Ph.D.,
and Sara Heggland, Ph.D.

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