Observational analysis reveals polyphosphate regulates cytosolic phosphate levels in cells, indicating a feedback mechanism for phosphate storage and release.
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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Bru et al. (2025) studied this question.
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