4.7 Article

Transcriptional response of Saccharomyces cerevisiae to potassium starvation

Journal

BMC GENOMICS
Volume 15, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/1471-2164-15-1040

Keywords

Saccharomyces cerevisiae; Cation homeostasis; SAGE tag sequencing; RNAseq; PHO84; Antisense RNA; Potassium starvation

Funding

  1. Netherlands Organization for Scientific Research (NWO) - Earth and Life Sciences (ALW) (SYSMO) [826.06.004, 826.09.006]

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Background: Ion homeostasis is essential for every cell and aberrant cation homeostasis is related to diseases like Alzheimer's disease and epilepsy. The mechanisms responsible for cation homeostasis are only partly understood. The yeast Saccharomyces cerevisiae is an excellent organism to study fundamental aspects of cation homeostasis. In this study we investigated the transcriptional response of this yeast to potassium starvation by using Serial Analysis of Gene Expression (SAGE)-tag sequencing. Results: Comparison of transcript levels in cells grown for 60 min in media without potassium with those in cells grown under standard potassium concentrations showed that the mRNA levels of 105 genes were significantly (P < 0.01) up-regulated more than 2.0-fold during potassium starvation and the mRNA levels of 172 genes significantly down-regulated. These genes belong to several functional categories. Genes involved in stress response including HSP30, YRO2 and TPO2 and phosphate metabolism including PHO84, PHO5 and SPL2 were highly up-regulated. Analysis of the promoter of PHO84 encoding a high affinity phosphate transporter, revealed that increased PHO84 RNA levels are caused by both increased Pho4-dependent transcription and decreased RNA turnover. In the latter process antisense transcription may be involved. Many genes involved in cell cycle control, and to a lesser extent genes involved in amino acid transport, were strongly down-regulated. Conclusions: Our study showed that yeast cells respond to potassium starvation in a complex way and reveals a direct link between potassium homeostasis and phosphate metabolism.

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