We propose to investigate the role of intracellular proteinases in the metabolism and differentiation of yeast cells. Mutants defective in known proteinases or in proteolytic processes have been and will be isolated and characterized. The effects of deficiency for the proteinase or proteolytic system on the biological and biochemical characteristics of the cells will be determined. Cellular processes to be scrutinized include cell growth and division, meiosis and sporulation, and protein degradation induced by starvation, sporulation or medium change. Mutants unable to degrade unstable proteins will be characterized for the spectrum of proteins rendered stable by the mutations (nonsense fragments, thermolabile enzymes, gluconeogenic enzymes upon medium shifts, etc.) The pep4-3 mutant will be examined further to see whether larger, inactive forms (possible precursors) of vacuolar enzymes accumulate in the mutant as has been found for proteinase C (carboxypeptidase Y). Similar studies will be conducted on a mutant of a new complementation group with properties similar to pep4-3.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases (NIADDK)
Type
Research Project (R01)
Project #
5R01AM018090-12
Application #
3151116
Study Section
Genetics Study Section (GEN)
Project Start
1977-08-01
Project End
1987-07-31
Budget Start
1985-08-01
Budget End
1986-07-31
Support Year
12
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Carnegie-Mellon University
Department
Type
Schools of Arts and Sciences
DUNS #
052184116
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
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Lemmon, S; Lemmon, V P; Jones, E W (1988) Characterization of yeast clathrin and anticlathrin heavy-chain monoclonal antibodies. J Cell Biochem 36:329-40
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