Abstract

The long term goal of this proposal is to elucidate the molecular mechanisms governing the tissue specific gene expression during development and differentiation of ocular lens. The primary focus is to understand the regulation of gamma-crystallin gene expression which will be subsequently extended to the other crystallin genes. The proposed study will be pursued in the following manner: The gamma-crystallin protein(s) will be isolated from Xenopus lens and polyclonal antibodies will be prepared. These antibodies will be employed for the proposed studies. The genomic clones containing the gamma 1 crystallin gene will be subcloned into a plasmid vector and characterized by DNA sequence analysis, gene copy number and hybrid-select translation. The DNA region(s) essential for the tissue specific expression will be identified by preparing a series of deleted, mutated and insertion genes. These will be introduced into either homologous or heterologous lens cells to assay for the specific expression. The developmental expression of gamma-crystallin gene will be undertaken both at the RNA and protein level and the results will be compared with the morphological changes associated with lens development. A tissue culture system will be developed from Xenopus eye lens epithelial cells to provide a homologous cell culture system which will subsequently be used for the transfection assay.

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY007498-03
Application #
3264415
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1988-05-01
Project End
1992-04-30
Budget Start
1990-05-01
Budget End
1992-04-30
Support Year
3
Fiscal Year
1990
Total Cost
Indirect Cost

  Institution

Name
Oakland University
Department
Type
Organized Research Units
DUNS #
City
Rochester
State
MI
Country
United States
Zip Code
48309