Yu Ai-Qun, Shi Tong-Lei, Zhang Biao, Xing Lai-Jun, Li Ming-Chun
Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, Department of Microbiology, Nankai University, Tianjin 300071, People's Republic of China.
Lipids. 2012 Nov;47(11):1099-108. doi: 10.1007/s11745-012-3712-z. Epub 2012 Sep 8.
Here we investigated the regulation of Pichia pastoris desaturase genes by low temperature and exogenous fatty acids in the late-exponential phase at the transcriptional level. Time-course studies of gene expression showed that mRNA levels of four desaturase genes were rapidly and transiently enhanced by low temperature and suppressed by exogenous oleic acid. Stearic acid showed no obvious repression of mRNA levels of Fad12 and Fad15 and a slight increase in Fad9A and Fad9B mRNA levels. Using a promoter-reporter gene construct, we demonstrated that the pFAD15 promoter activity was induced by low temperature in a time-dependent manner and reduced in a dose- and time-dependent manner by unsaturated fatty acids. Also, there was no absolute correlation between mRNA abundance and production of corresponding fatty acids. Disruption of Spt23 resulted in a decrease in transcript levels of Fad9A and Fad9B, but had little effect on the other desaturase genes. Consistent with these observations, a decrease in the relative amount of oleic acid (OLA) and an increase in the relative content of linoleic acid and ALA with different degrees were clearly observed in the stationary phase cells of ΔSpt23 mutant. Further analysis showed that the effect of low-temperature activation and OLA inhibition on expression of Fad9A and Fad9B seemed to disappear after disruption of the Spt23 gene, which indicated that Spt23p is essential for the expression of two Δ9-desaturase genes internally and probably involved in the regulation of Δ9-desaturase genes transcription in response to external stimuli, and thereby plays a role in the synthesis of OLA.
在此,我们在转录水平上研究了低温和外源脂肪酸对毕赤酵母去饱和酶基因在指数生长后期的调控。基因表达的时间进程研究表明,4个去饱和酶基因的mRNA水平在低温下迅速且短暂地增强,而在外源油酸作用下受到抑制。硬脂酸对Fad12和Fad15的mRNA水平没有明显的抑制作用,对Fad9A和Fad9B的mRNA水平有轻微的增加作用。利用启动子 - 报告基因构建体,我们证明pFAD15启动子活性在低温下呈时间依赖性诱导,而在不饱和脂肪酸作用下呈剂量和时间依赖性降低。此外,mRNA丰度与相应脂肪酸的产生之间没有绝对的相关性。Spt23的缺失导致Fad9A和Fad9B的转录水平下降,但对其他去饱和酶基因影响不大。与这些观察结果一致,在ΔSpt23突变体的稳定期细胞中,明显观察到油酸(OLA)相对含量降低,亚油酸和ALA相对含量不同程度增加。进一步分析表明,在Spt23基因缺失后,低温激活和OLA抑制对Fad9A和Fad9B表达的影响似乎消失了,这表明Spt23p对于两个Δ9 - 去饱和酶基因的内部表达至关重要,并且可能参与了响应外部刺激的Δ9 - 去饱和酶基因转录调控,从而在OLA的合成中发挥作用。