The goal of this research is to elucidate the mechanisms of eucaryotic gene regulation. The system chosen for study is the yeast transcriptional activator ADR1 in its control of glucose repressible alcohol dehydrogenase (ADH2). Particular emphasis will be placed on defining the mechanisms by which ADR1 is regulated, the functional regions of ADr1, the factors which mediate or influence ADr1 functions, and the means by which these factors and ADR1 control ADH2 transcription. A combination of biochemical, recombinant DNA, and genetic analyses will be used. The activation/repression domains of ADR1 will be precisely identified and their interactions will be analyzed. The mechanism by which an ADR1 mutation enhances the function of ADR1 activation domains will be examined by determining its effect on dimerization, ADR1 conformation, and binding of other proteins. The proteins which co-immuneprecipitate with ADR1 will be purified and characterized. %%%% The goal of this research is to understand how cells respond to the environment and control when and which genes the expression will be characterized by identifying their important regions. These regions include segments that respond to the environmental signals, that contact other proteins, and that turn on or off the express of genes. A combination of genetic, recombinant DNA, and biochemical techniques will be used.

Agency
National Science Foundation (NSF)
Institute
Division of Molecular and Cellular Biosciences (MCB)
Application #
9218728
Program Officer
karen kindle-hartsuyker
Project Start
Project End
Budget Start
1993-04-01
Budget End
1997-03-31
Support Year
Fiscal Year
1992
Total Cost
$270,000
Indirect Cost
Name
University of New Hampshire
Department
Type
DUNS #
City
Durham
State
NH
Country
United States
Zip Code
03824