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酿酒酵母中缺乏14-3-3蛋白会导致Pho4调控基因SPL2和PHO84表达的细胞间异质性。

Lack of 14-3-3 proteins in Saccharomyces cerevisiae results in cell-to-cell heterogeneity in the expression of Pho4-regulated genes SPL2 and PHO84.

作者信息

Teunissen Janneke H M, Crooijmans Marjolein E, Teunisse Pepijn P P, van Heusden G Paul H

机构信息

Institute of Biology, Leiden University, Sylviusweg 72, NL-2333BE, Leiden, the Netherlands.

出版信息

BMC Genomics. 2017 Sep 6;18(1):701. doi: 10.1186/s12864-017-4105-8.

Abstract

BACKGROUND

Ion homeostasis is an essential property of living organisms. The yeast Saccharomyces cerevisiae is an ideal model organism to investigate ion homeostasis at all levels. In this yeast genes involved in high-affinity phosphate uptake (PHO genes) are strongly induced during both phosphate and potassium starvation, indicating a link between phosphate and potassium homeostasis. However, the signal transduction processes involved are not completely understood. As 14-3-3 proteins are key regulators of signal transduction processes, we investigated the effect of deletion of the 14-3-3 genes BMH1 or BMH2 on gene expression during potassium starvation and focused especially on the expression of genes involved in phosphate uptake.

RESULTS

Genome-wide analysis of the effect of disruption of either BMH1 or BMH2 revealed that the mRNA levels of the PHO genes PHO84 and SPL2 are greatly reduced in the mutant strains compared to the levels in wild type strains. This was especially apparent at standard potassium and phosphate concentrations. Furthermore the promoter of these genes is less active after deletion of BMH1. Microscopic and flow cytometric analysis of cells with GFP-tagged SPL2 showed that disruption of BMH1 resulted in two populations of genetically identical cells, cells expressing the protein and the majority of cells with no detectible expression. Heterogeneity was also observed for the expression of GFP under control of the PHO84 promoter. Upon deletion of PHO80 encoding a regulator of the transcription factor Pho4, the effect of the BMH1 deletion on SPL2 and PHO84 promoter was lost, suggesting that the BMH1 deletion mainly influences processes upstream of the Pho4 transcription factor.

CONCLUSION

Our data indicate that that yeast cells can be in either of two states, expressing or not expressing genes required for high-affinity phosphate uptake and that 14-3-3 proteins are involved in the process(es) that establish the activation state of the PHO regulon.

摘要

背景

离子稳态是生物体的一项基本特性。酿酒酵母是在各个层面研究离子稳态的理想模式生物。在这种酵母中,参与高亲和力磷酸盐摄取的基因(PHO基因)在磷酸盐和钾饥饿期间均被强烈诱导,这表明磷酸盐和钾稳态之间存在联系。然而,所涉及的信号转导过程尚未完全明确。由于14-3-3蛋白是信号转导过程的关键调节因子,我们研究了14-3-3基因BMH1或BMH2缺失对钾饥饿期间基因表达的影响,尤其关注参与磷酸盐摄取的基因的表达。

结果

对BMH1或BMH2缺失效应的全基因组分析表明,与野生型菌株相比,突变菌株中PHO基因PHO84和SPL2的mRNA水平大幅降低。这在标准钾和磷酸盐浓度下尤为明显。此外,BMH1缺失后这些基因的启动子活性较低。对带有绿色荧光蛋白标记的SPL2的细胞进行显微镜和流式细胞术分析表明,BMH1缺失导致了两个基因相同的细胞群体,即表达该蛋白的细胞和大多数无法检测到表达的细胞。在PHO84启动子控制下的绿色荧光蛋白表达也观察到了异质性。缺失编码转录因子Pho4调节因子的PHO80后,BMH1缺失对SPL2和PHO84启动子的影响消失,这表明BMH1缺失主要影响Pho4转录因子上游的过程。

结论

我们的数据表明,酵母细胞可以处于两种状态之一,即表达或不表达高亲和力磷酸盐摄取所需的基因,并且14-3-3蛋白参与了建立PHO调节子激活状态的过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9a8/5588707/e2bacda6356f/12864_2017_4105_Fig1_HTML.jpg

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