首页> 美国卫生研究院文献>Journal of Bacteriology >Analysis of Phosphorylated Sphingolipid Long-Chain Bases Reveals Potential Roles in Heat Stress and Growth Control in Saccharomyces
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Analysis of Phosphorylated Sphingolipid Long-Chain Bases Reveals Potential Roles in Heat Stress and Growth Control in Saccharomyces

机译:磷酸化的鞘脂长链碱基的分析揭示了在酿酒酵母中热应激和生长控制中的潜在作用

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摘要

Sphingolipid long-chain bases and their phosphorylated derivatives, for example, sphingosine-1-phosphate in mammals, have been implicated as signaling molecules. The possibility that Saccharomyces cerevisiae cells also use long-chain-base phosphates to regulate cellular processes has only recently begun to be examined. Here we present a simple and sensitive procedure for analyzing and quantifying long-chain-base phosphates in S. cerevisiae cells. Our data show for the first time that phytosphingosine-1-phosphate (PHS-1-P) is present at a low but detectable level in cells grown on a fermentable carbon source at 25°C, while dihydrosphingosine-1-phosphate (DHS-1-P) is only barely detectable. Shifting cells to 37°C causes transient eight- and fivefold increases in levels of PHS-1-P and DHS-1-P, respectively, which peak after about 10 min. The amounts of both compounds return to the unstressed levels by 20 min after the temperature shift. These data are consistent with PHS-1-P and DHS-1-P being signaling molecules. Cells unable to break down long-chain-base phosphates, due to deletion of DPL1 and LCB3, show a 500-fold increase in PHS-1-P and DHS-1-P levels, grow slowly, and survive a 44°C heat stress 10-fold better than parental cells. These and other data for dpl1 or lcb3 single-mutant strains suggest that DHS-1-P and/or PHS-1-P act as signals for resistance to heat stress. Our procedure should expedite experiments to determine how the synthesis and breakdown of these compounds is regulated and how the compounds mediate resistance to elevated temperature.
机译:鞘脂脂长链碱基及其磷酸化衍生物,例如哺乳动物中的鞘氨醇-1-磷酸,已被认为是信号分子。酿酒酵母细胞也使用长链磷酸酯调节细胞过程的可能性只是最近才开始研究。在这里,我们提出了一种简单而灵敏的程序,用于分析和定量酿酒酵母细胞中的长链碱基磷酸盐。我们的数据首次显示,在25°C的可发酵碳源上生长的细胞中,植物磷酸鞘氨醇1-磷酸(PHS-1-P)的含量较低,但可检测到,而磷酸二氢鞘氨醇1-磷酸酯(DHS- 1-P)几乎无法检测到。将细胞移至37°C会导致PHS-1-P和DHS-1-P的水平分别瞬时升高8倍和5倍,在约10分钟后达到峰值。在温度变化后20分钟,两种化合物的量都恢复到未加应力的水平。这些数据与作为信号分子的PHS-1-P和DHS-1-P一致。由于DPL1和LCB3缺失,无法分解长链磷酸根的细胞显示PHS-1-P和DHS-1-P水平增加500倍,生长缓慢,并在44°C的高温下存活压力比亲代细胞好10倍。 dpl1或lcb3单突变株的这些数据和其他数据表明DHS-1-P和/或PHS-1-P充当了抗热胁迫的信号。我们的程序应加快实验速度,以确定如何调节这些化合物的合成和分解,以及这些化合物如何介导对高温的抵抗力。

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