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Regulation of the Na+/K+-ATPase Ena1 Expression by Calcineurin/Crz1 under High pH Stress: A Quantitative Study

Authors: Silvia Petrezsélyová; María López-Malo; David Canadell; Alicia Roque; Albert Serra-Cardona; M. Carmen Marqués; Ester Vilaprinyó; +3 Authors

Regulation of the Na+/K+-ATPase Ena1 Expression by Calcineurin/Crz1 under High pH Stress: A Quantitative Study

Abstract

Regulated expression of the Ena1 Na+-ATPase is a crucial event for adaptation to high salt and/or alkaline pH stress in the budding yeast Saccharomyces cerevisiae. ENA1 expression is under the control of diverse signaling pathways, including that mediated by the calcium-regulatable protein phosphatase calcineurin and its downstream transcription factor Crz1. We present here a quantitative study of the expression of Ena1 in response to alkalinization of the environment and we analyze the contribution of Crz1 to this response. Experimental data and mathematical models substantiate the existence of two stress-responsive Crz1-binding sites in the ENA1 promoter and estimate that the contribution of Crz1 to the early response of the ENA1 promoter is about 60%. The models suggest the existence of a second input with similar kinetics, which would be likely mediated by high pH-induced activation of the Snf1 kinase.

Keywords

Alkaline pH stress, Saccharomyces cerevisiae Proteins, Science, Microfluidics, DNA transcription, Active Transport, Cell Nucleus, Saccharomyces cerevisiae, Protein accumulation, Cation homeostasis, Gene Expression Regulation, Enzymologic, mRNA levels, Investigació quantitativa, Stress, Physiological, Cations, Gene Expression Regulation, Fungal, Transcription rate, BIOQUIMICA Y BIOLOGIA MOLECULAR, Transcription factors, Regulation of gene expression, Regulatory Elements, Transcriptional, Quantitative analysis, Promoter Regions, Genetic, Crz1, Transcription factor, Recombinant proteins, Cell Nucleus, Binding Sites, Organisms, Genetically Modified, Messenger RNA, Calcineurin, Q, R, Hydrogen-Ion Concentration, Yeast, DNA-Binding Proteins, RNA denaturation, Protein Transport, Protein phosphatase, Medicine, Llevats, Sodium-Potassium-Exchanging ATPase, Research Article, Transcription Factors

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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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