Acidocalcisome-like vacuoles constitute a feedback-controlled phosphate buffering system for the cytosol

Cells experience strong variations in the consumption and availability of inorganic phosphate (P<sub>i</sub>). Since P<sub>i</sub> is an essential macronutrient but excess P<sub>i</sub> has negative impacts on nucleotide hydrolysis and metabolism, its concentration must be maintained in a suitable range. Conserved storage organelles, acidocalcisomes, provide this buffering function. We used acidocalcisome-like yeast vacuoles to study how such organelles are set up to perform this task. Our combined in vitro and in vivo analyses revealed that their ATP-driven polyphosphate polymerase VTC converts cytosolic P<sub>i</sub> into inorganic polyphosphates (polyP), which it transfers into the vacuole lumen. Luminal polyphosphatases immediately hydrolyse this polyP to establish a growing reservoir of vacuolar P<sub>i</sub>. Product inhibition by this P<sub>i</sub> pool silences the polyphosphatases, caps P<sub>i</sub> accumulation, and favours vacuolar polyP storage. Upon cytosolic P<sub>i</sub> scarcity, the declining inositol pyrophosphate levels activate the vacuolar P<sub>i</sub> exporter Pho91 to replenish cytosolic P<sub>i</sub>. In this way, acidocalcisome-like vacuoles constitute a feedback-regulated buffering system for cytosolic P<sub>i</sub>, which the cells can switch between P<sub>i</sub> accumulation, P<sub>i</sub> release, and high-capacity phosphate storage through polyP.

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Journal
eLife
Published
2025-08-22
DOI
https://doi.org/10.7554/elife.108181
Citations
1
Primary Topic
Cellular transport and secretion
Type
article
Field-Weighted Citation Impact
1.15

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article

Acidocalcisome-like vacuoles constitute a feedback-controlled phosphate buffering system for the cytosol

Henning Jacob Jessen, Lydie Michaillat Mayer, Geun-Don Kim, Danye Qiu et al.
1 citations
eLife
Cellular transport and secretion
1.15
article

Acidocalcisome-like vacuoles constitute a feedback-controlled phosphate buffering system for the cytosol

Henning Jacob Jessen, Lydie Michaillat Mayer, Geun-Don Kim, Danye Qiu, Andreas Mayer, Samuel Bru
article en
1 citations

Abstract

Cells experience strong variations in the consumption and availability of inorganic phosphate (P<sub>i</sub>). Since P<sub>i</sub> is an essential macronutrient but excess P<sub>i</sub> has negative impacts on nucleotide hydrolysis and metabolism, its concentration must be maintained in a suitable range. Conserved storage organelles, acidocalcisomes, provide this buffering function. We used acidocalcisome-like yeast vacuoles to study how such organelles are set up to perform this task. Our combined in vitro and in vivo analyses revealed that their ATP-driven polyphosphate polymerase VTC converts cytosolic P<sub>i</sub> into inorganic polyphosphates (polyP), which it transfers into the vacuole lumen. Luminal polyphosphatases immediately hydrolyse this polyP to establish a growing reservoir of vacuolar P<sub>i</sub>. Product inhibition by this P<sub>i</sub> pool silences the polyphosphatases, caps P<sub>i</sub> accumulation, and favours vacuolar polyP storage. Upon cytosolic P<sub>i</sub> scarcity, the declining inositol pyrophosphate levels activate the vacuolar P<sub>i</sub> exporter Pho91 to replenish cytosolic P<sub>i</sub>. In this way, acidocalcisome-like vacuoles constitute a feedback-regulated buffering system for cytosolic P<sub>i</sub>, which the cells can switch between P<sub>i</sub> accumulation, P<sub>i</sub> release, and high-capacity phosphate storage through polyP.

eLifeVol. 14
University of Freiburg (DE), Universitat Internacional de Catalunya (ES), University of Lausanne (CH)
Deutsche Forschungsgemeinschaft, Volkswagen Foundation, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Openalex Percentile: Top 21%
Cellular transport and secretion
1.15
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