Melinda K. Duncan, Ph.D.

Assistant Professor
Department of Biological Sciences
Laboratory: 340 Wolf Hall    Office: 331 Wolf Hall
The University of Delaware
Newark, DE 19716-2590 USA
Phone (302) 831-0533
FAX (302) 831-2281
E-mail: Duncanm@udel.edu

Course page for BISC667: "Developmental Biology"
 

Research opportunities:
 
    Research opportunities exist in my laboratory for both graduate and undergraduate students interested in the molecular control of vertebrate development. Please e-mail me if you're interested in starting a research project in vertebrate eye development.
 


Research Interests:

INTRODUCTION
    The laboratory investigates the molecular mechanisms responsible for the terminal differentiation of cells and organs and how the disruption of these pathways leads to disease.  Over the past several years,  these questions have been studied in the developing eye and more specifically the lens.  The lens is a good model to study organogenesis since it, like many other tissues, requires early inductive events between different germinative layers for its development. In addition, the lens is a relatively simple organ, consisting only of a proliferative epithelial layer overlying terminally differentiated fiber cells.  As cells leave the germinative zone of the epithelium, they begin to elongate, express terminal differentiation markers and finally degrade their nuclei and cellular organelles in preparation for lens transparency.  Lens development and physiology can be easily perturbed in vivo  by targeted gene expression since the disruption of lens development does not affect survival.  Also, numerous spontaneous mouse mutations with abnormal eyes and lenses are known and can be used as tools to help understand normal development and as models of human eye diseases.

     Crystallins, the major water soluble proteins of the lens, are a diverse group of proteins whose expression either commences or sharply upregulates during the elongation of lens fiber cells.  The ability of the lens to focus light is a direct result of the refractive index formed by the high levels of these proteins found in the lens.  Each crystallin gene has its own temporal and spatial expression pattern during development resulting in a refractive index gradient which prevents spherical aberration in the short focal length vertebrate lens.  I have investigated the developmental pathways responsible for the formation of a functional lens by studying the mechanisms responsible for the high level of crystallin expression in the lens, the genes involved in the early specification of the lens, as well as the role of crystallins in the maintenance of lens transparency.
 

More Details:

CRYSTALLINS AS MARKERS OF LENS DIFFERENTIATION

STRUCTURE AND EXPRESSION OF BETA-CRYSTALLINS
 

    Finally, I would be greatly interested in collaborating with both clinical and basic scientists to develop other projects related to development and disease in vertebrates.

 

Recent publications:

Other Links of Interest:

Mouse genome informatics:



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Last updated 11/10/97