首页> 外文OA文献 >Inositol transport in Saccharomyces cerevisiae is regulated by transcriptional and degradative endocytic mechanisms during the growth cycle that are distinct from inositol-induced regulation.
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Inositol transport in Saccharomyces cerevisiae is regulated by transcriptional and degradative endocytic mechanisms during the growth cycle that are distinct from inositol-induced regulation.

机译:酿酒酵母中的肌醇运输受生长周期中转录和降解内吞机制的调节,这与肌醇诱导的调节不同。

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摘要

Regulation of inositol uptake activity in Saccharomyces cerevisiae during the growth cycle was examined. Activity increased as the cell population transited from lag phase to exponential growth, and continued to increase until late exponential phase. The increase in activity was due to increased transcription of the ITR1 gene and synthesis of the Itr1 permease. When the culture reached stationary phase, uptake activity decreased and dropped to a minimum within 4 h. The decrease was due to repression of ITR1 transcription, independent of the negative regulator Opi1p, and degradation of the existing permease. Degradation depended on delivery of the permease to the vacuole through the END3/END4 endocytic pathway. During exponential growth in inositol-containing medium the permease is also rapidly degraded, whereas in inositol-free medium the permease is highly stable. Rapid degradation of the permease at stationary phase occurred in inositol-free medium, indicating that there are two distinct mechanisms that trigger endocytosis and degradation in response to different physiological stimuli. In addition, the level of the enzyme required for inositol biosynthesis, inositol-1-phosphate synthase, encoded by INO1, is not reduced in stationary-phase cells, and this contrast in the regulation of inositol supply is discussed.
机译:检查了酿酒酵母在生长周期中肌醇摄取活性的调节。活性随着细胞群体从滞后阶段过渡到指数增长而增加,并持续增加直到指数后期。活性的增加归因于ITR1基因的转录增加和Itr1通透酶的合成。当培养物达到固定相时,摄取活性降低,并在4小时内降至最低。减少归因于ITR1转录的抑制(独立于负调控因子Opi1p)和现有通透酶的降解。降解取决于渗透酶通过END3 / END4内吞途径向液泡的传递。在含肌醇的培养基中指数增长期间,渗透酶也迅速降解,而在无肌醇的培养基中,渗透酶高度稳定。固定相上通透酶的快速降解发生在无肌醇的培养基中,表明存在两种不同的机制可触发内吞和响应不同的生理刺激而降解。另外,由INO1编码的肌醇生物合成所需的酶,肌醇-1-磷酸合酶的水平在固定相细胞中并未降低,并讨论了肌醇供应调节中的这种对比。

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