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 i ). Since P i is an essential macronutrient but excess P i 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 i 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 i . Product inhibition by this P i pool silences the polyphosphatases, caps P i accumulation, and favours vacuolar polyP storage. Upon cytosolic P i scarcity, the declining inositol pyrophosphate levels activate the vacuolar P i exporter Pho91 to replenish cytosolic P i . In this way, acidocalcisome-like vacuoles constitute a feedback-regulated buffering system for cytosolic P i , which the cells can switch between P i accumulation, P i release, and high-capacity phosphate storage through polyP.

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Journal
eLife
Published
2025-12-01
DOI
https://doi.org/10.7554/elife.108181.3
Primary Topic
Coagulation, Bradykinin, Polyphosphates, and Angioedema
Type
article
Field-Weighted Citation Impact
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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.
eLife
Coagulation, Bradykinin, Polyphosphates, and Angioedema
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

Abstract

Cells experience strong variations in the consumption and availability of inorganic phosphate (P i ). Since P i is an essential macronutrient but excess P i 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 i 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 i . Product inhibition by this P i pool silences the polyphosphatases, caps P i accumulation, and favours vacuolar polyP storage. Upon cytosolic P i scarcity, the declining inositol pyrophosphate levels activate the vacuolar P i exporter Pho91 to replenish cytosolic P i . In this way, acidocalcisome-like vacuoles constitute a feedback-regulated buffering system for cytosolic P i , which the cells can switch between P i accumulation, P i release, and high-capacity phosphate storage through polyP.

eLifeVol. 14
University of Freiburg (DE), Universitat Internacional de Catalunya (ES), University of Lausanne (CH)
Openalex Percentile: Top 46%
Coagulation, Bradykinin, Polyphosphates, and Angioedema
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