Abstract
The Saccharomyces cerevisiae PEP4 gene encodes proteinase A, an aspartyl protease. pep4 mutants are defective in the activation of many vacuolar hydrolases, including proteinase B. We have expressed a pep4 mutation which directs the accumulation of pro‐proteinase A with a defective active site. Co‐expression with PEP4 leads to normal processing, i.e. the mutant zymogen is functional as a substrate for the maturation reaction in trans. We conclude that wild‐type pro‐proteinase A has the ability to mediate its own activation. Elimination of the co‐expressed PEP4 gene did not effectively stop the processing of the mutant zymogen, owing to a strong, proteinase‐B‐dependent, phenotypic lag. In a proteinase‐B‐negative strain, processing of pro‐proteinase A led to an active form of a higher molecular mass than the normal mature form. Copyright © 1992, Wiley Blackwell. All rights reserved
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CITATION STYLE
van den HAZEL, H. B., KIELLAND‐BRANDT, M. C., & WINTHER, J. R. (1992). Autoactivation of proteinase A initiates activation of yeast vacuolar zymogens. European Journal of Biochemistry, 207(1), 277–283. https://doi.org/10.1111/j.1432-1033.1992.tb17048.x
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