Protein degradation, meiosis and sporulation in proteinase-deficient mutants of Saccharomyces cerevisiae.
Protein degradation, meiosis and sporulation in proteinase-deficient mutants of Saccharomyces cerevisiae.
复制标题
酿酒酵母蛋白酶缺陷突变体的蛋白质降解、减数分裂和孢子形成。
DOI:
10.1093/genetics/97.1.45
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发表时间:
1981
期刊:
影响因子:
3.3
通讯作者:
Jones,EW
中科院分区:
文献类型:
--
作者:
Zubenko,GS;Jones,EW
During the process of sporulation,a/α diploids degrade about 50% of their vegetative proteins. This degradation is not sporulation specific, for asporogenous diploids ofa/amating type degrade their vegetative proteins in a fashion similar to that of theira/α counterparts. Diploids lacking carboxypeptidase Y activity,prc1/prc1, show about 80% of wild-type levels of protein degradation, but are unimpaired in the production of normal asci. Diploids lacking proteinase B activity,prb1/prb1, show about 50% of wild-type levels of protein degradation. The effect on degradation of the proteinase B deficiency is epistatic to the degradation deficit attributable to the carboxypeptidase Y deficiency. Theprb1homozygotes undergo meiosis and produce spores, but the asci and, possibly, the spores are abnormal. Diploids homozygous for the pleiotropicpep4-3mutation show only 30% of the wild-type levels of degradation when exposed to a sporulation regimen, and do not undergo meiosis or sporulation. Neither proteinase B nor carboxypeptidase Y is necessary for germination of spores. ——Approximately half of the colonies arising froma/aor α/α diploids exposed to the sporulation regiment that express an initially heterozygous drug-resistance marker (can1) appear to arise from mating-type switches followed by meiosis and sporulation.