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高尔基体在酿酒酵母vps33Delta液泡生物发生突变体的Ca2+稳态维持中发挥着重要作用。

The Golgi apparatus plays a significant role in the maintenance of Ca2+ homeostasis in the vps33Delta vacuolar biogenesis mutant of Saccharomyces cerevisiae.

作者信息

Miseta A, Fu L, Kellermayer R, Buckley J, Bedwell D M

机构信息

Department of Microbiology, the University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.

出版信息

J Biol Chem. 1999 Feb 26;274(9):5939-47. doi: 10.1074/jbc.274.9.5939.

Abstract

The vacuole is the major site of intracellular Ca2+ storage in yeast and functions to maintain cytosolic Ca2+ levels within a narrow physiological range. In this study, we examined how cellular Ca2+ homeostasis is maintained in a vps33Delta vacuolar biogenesis mutant. We found that growth of the vps33Delta strain was sensitive to high or low extracellular Ca2+. This strain could not properly regulate cytosolic Ca2+ levels and was able to retain only a small fraction of its total cellular Ca2+ in a nonexchangeable intracellular pool. Surprisingly, the vps33Delta strain contained more total cellular Ca2+ than the wild type strain. Because most cellular Ca2+ is normally found within the vacuole, this suggested that other intracellular compartments compensated for the reduced capacity to store Ca2+ within the vacuole of this strain. To test this hypothesis, we examined the contribution of the Golgi-localized Ca2+ ATPase Pmr1p in the maintenance of cellular Ca2+ homeostasis. We found that a vps33Delta/pmr1Delta strain was hypersensitive to high extracellular Ca2+. In addition, certain combinations of mutations effecting both vacuolar and Golgi Ca2+ transport resulted in synthetic lethality. These results indicate that the Golgi apparatus plays a significant role in maintaining Ca2+ homeostasis when vacuolar biogenesis is compromised.

摘要

液泡是酵母细胞内储存Ca2+的主要场所,其功能是将胞质Ca2+水平维持在狭窄的生理范围内。在本研究中,我们研究了vps33Delta液泡生物发生突变体中细胞Ca2+稳态是如何维持的。我们发现vps33Delta菌株的生长对高或低细胞外Ca2+敏感。该菌株不能正确调节胞质Ca2+水平,只能将其总细胞Ca2+的一小部分保留在不可交换的细胞内池中。令人惊讶的是,vps33Delta菌株的总细胞Ca2+含量比野生型菌株多。由于大多数细胞Ca2+通常存在于液泡中,这表明其他细胞内区室补偿了该菌株液泡中Ca2+储存能力的降低。为了验证这一假设,我们研究了高尔基体定位的Ca2+ ATPase Pmr1p在维持细胞Ca2+稳态中的作用。我们发现vps33Delta/pmr1Delta菌株对高细胞外Ca2+高度敏感。此外,影响液泡和高尔基体Ca2+转运的某些突变组合导致合成致死。这些结果表明,当液泡生物发生受损时,高尔基体在维持Ca2+稳态中起重要作用。

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