The objective of this grant request is to utilize molecular biological techniques for analyzing differences in the regulation of genetic information in normal and genetically-altered lenses leading to the formation of cataract and other disorders. In order to fully understand the mechanisms underlying lens diseases at molecular level, molecular cloning of crystallin genes and DNA sequencing of cloned fragments will be performed. Together with the cloning methods, cell culture techniques will be employed to generate sufficient genetic materials, from normal and genetically-linked lens systems. The molecular differentiation of normal and genetically-defected lens cells will be investigated through molecular induction of specific retinal and vitreous factors isolated from various developmental stages of the embryonic eye tissue.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY003173-07
Application #
3257446
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1979-03-01
Project End
1986-10-31
Budget Start
1984-12-01
Budget End
1986-10-31
Support Year
7
Fiscal Year
1985
Total Cost
Indirect Cost
Name
New York University
Department
Type
Schools of Dentistry/Oral Hygn
DUNS #
004514360
City
New York
State
NY
Country
United States
Zip Code
10012
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Gagna, C E; Mitchell, O G; Chen, J H (1991) Fixation and immunolocalization of left-handed Z-DNA sequences in the calf lens. Lens Eye Toxic Res 8:489-509
Chen, J H; Tong, T C; Zhang, L (1991) Rapid enhancement of ""MIP"" 26kDa protein phosphorylation by RF-36 nucleic acid binding protein in lens cells. Lens Eye Toxic Res 8:469-87
Gagna, C E; Chen, J H; Lavers, G C et al. (1991) The presence of Z-helical conformation in DNA of the calf lens. Lens Eye Toxic Res 8:27-42