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酿酒酵母MATa突变细胞在高浓度α-因子作用下,响应α-因子时形成尖状突起存在缺陷。

Saccharomyces cerevisiae MATa mutant cells defective in pointed projection formation in response to alpha-factor at high concentrations.

作者信息

Yorihuzi T, Ohsumi Y

机构信息

Department of Biology, College of Arts and Sciences, University of Tokyo, Japan.

出版信息

Yeast. 1994 May;10(5):579-94. doi: 10.1002/yea.320100503.

Abstract

We have isolated Saccharomyces cerevisiae MATa mutant cells that do not form a pointed projection but elongate in response to alpha-factor at high concentrations. Complementation tests defined three genes, PPF1, PPF2, and PPF3 (for pointed projection formation), necessary for pointed projection formation. Allelism tests with genes known to be needed for projection formation revealed that PPF1 is identical to SPA2, while PPF2 and PPF3 are not allelic to SST2, STE2, SPA2, BEM1 or SLK1/SSP31/BCK1. The morphology of MATa ppf mutants treated with high concentrations of alpha-factor is similar to that of MATa PPF cells treated with alpha-factor at low concentrations. Quantitative mating tests showed that PPF2 and PPF3 are not essential for mating in either MATa or MAT alpha background. Monitoring of division arrest and expression of an alpha-factor-inducible gene revealed that mutations in the PPF genes do not affect the responses of MATa cells to low concentrations of alpha-factor. Unlike wild-type cells, the ppf mutants exhibited early recovery from alpha-factor-induced division arrest. Furthermore, vegetatively growing ppf3-1 cells are slightly defective in cell separation of mother and daughter cells and in selection of the correct bud sites in all cell types. These results indicate that PPF2 and PPF3 are involved in the response to alpha-factor at high concentrations and that PPF3 is also required for proper establishment of polarity in vegetative growth.

摘要

我们分离出了酿酒酵母MATa突变体细胞,这些细胞不会形成尖状突起,而是在高浓度α因子作用下伸长。互补试验确定了三个基因,PPF1、PPF2和PPF3(用于尖状突起形成),它们是尖状突起形成所必需的。与已知参与突起形成的基因进行等位性测试表明,PPF1与SPA2相同,而PPF2和PPF3与SST2、STE2、SPA2、BEM1或SLK1/SSP31/BCK1不等位。用高浓度α因子处理的MATa ppf突变体的形态与用低浓度α因子处理的MATa PPF细胞的形态相似。定量交配试验表明,PPF2和PPF3在MATa或MATα背景下对交配都不是必需的。对分裂停滞和α因子诱导基因表达的监测表明,PPF基因的突变不会影响MATa细胞对低浓度α因子的反应。与野生型细胞不同,ppf突变体在α因子诱导的分裂停滞中表现出早期恢复。此外,营养生长的ppf3-1细胞在母细胞和子细胞的细胞分离以及所有细胞类型中正确芽位点的选择上略有缺陷。这些结果表明,PPF2和PPF3参与了对高浓度α因子的反应,并且PPF3在营养生长中正确建立极性方面也是必需的。

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