THE PROTEINASE YSCA-INHIBITOR, IA3, GENE - STUDIES OF CYTOPLASMIC PROTEINASE-INHIBITOR DEFICIENCY ON YEAST PHYSIOLOGY

被引:14
作者
SCHU, P
WOLF, DH
机构
[1] UNIV STUTTGART,INST BIOCHEM,PFAFFENWALDRING 55,W-7000 STUTTGART 80,GERMANY
[2] UNIV FREIBURG,INST BIOCHEM,W-7800 FREIBURG,GERMANY
关键词
PROTEOLYSIS; PROTEINASE INHIBITOR; IA3; IB2; NULL MUTANT; SACCHAROMYCES-CEREVISIAE;
D O I
10.1016/0014-5793(91)80558-K
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gene of the proteinase yscA inhibitor I(A)3, PAI3, of the yeast Saccharomyces cerevisiae was isolated by oligonucleotide screening of a genomic DNA library and sequenced. The gene codes for a single protein of 68 amino acids. The structural PAI3 gene was deleted in vitro by oligonucleotide-site-directed mutagenesis. The mutated allele was introduced via homologous recombination into the genome of wild-type yeast and into the genome of a yeast mutant, which lacks the second cytoplasmic proteinase-inhibitor, I(B)2. The deficiency of either or of both inhibitors has no effect on the cell viability under various physiological conditions. The inhibitor mutants, however, show an increase in the general in vivo protein degradation rate. The I(A)3 mutant has a 2-3-fold increased protein degradation rate in the first 6 h after a shift from rich medium onto starvation-medium, whereas the I(B)2 mutant shows a constantly increased degradation rate of 20-50% under the same conditions. The inhibitor double null mutant has the same protein degradation rate as the I(A)3 null mutant. These results suggest an in vivo interaction between the vacuolor endopeptidases and their cytoplasmic inhibitors.
引用
收藏
页码:78 / 84
页数:7
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