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酿酒酵母中的肌醇转运在生长周期中受转录和降解性内吞机制调控,这些机制不同于肌醇诱导的调控。

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

作者信息

Robinson K S, Lai K, Cannon T A, McGraw P

机构信息

Department of Biological Sciences, University of Maryland at Baltimore County, Catonsville, Maryland 21228, USA.

出版信息

Mol Biol Cell. 1996 Jan;7(1):81-9. doi: 10.1091/mbc.7.1.81.

Abstract

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.

摘要

研究了酿酒酵母生长周期中肌醇摄取活性的调控。随着细胞群体从延迟期过渡到指数生长期,活性增加,并持续增加直至指数生长期后期。活性的增加是由于ITR1基因转录增加和Itr1通透酶的合成。当培养物达到稳定期时,摄取活性下降并在4小时内降至最低。这种下降是由于ITR1转录的抑制,独立于负调节因子Opi1p,以及现有通透酶的降解。降解依赖于通透酶通过END3/END4内吞途径输送到液泡。在含肌醇培养基中指数生长期间,通透酶也迅速降解,而在无肌醇培养基中通透酶高度稳定。在无肌醇培养基中,稳定期通透酶迅速降解,表明存在两种不同的机制,可响应不同的生理刺激触发内吞作用和降解。此外,由INO1编码的肌醇生物合成所需的酶肌醇-1-磷酸合酶的水平在稳定期细胞中并未降低,并讨论了肌醇供应调控中的这种差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d93/278614/ab4a815c34ce/mbc00008-0090-a.jpg

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