The compartmentalization of metabolic enzymes into membraneless filaments termed cytoophidia represents a conserved regulatory mechanism, exemplified by cytidine triphosphate synthase (CTPS), which assembles into pH-sensitive cytoophidia in the cytosol. In Saccharomyces cerevisiae, nutritional deprivation both triggers CTPS cytoophidia assembly and disassembles the vacuolar H⁺-ATPase (V-ATPase) that acidifies vacuoles (lysosomes), yet whether these processes are functionally linked remains unknown. We demonstrate spatial proximity between the yeast CTPS homologues Ura7/Ura8, the V-ATPase, and the AP-3 adaptor complex that mediates vesicular transport to vacuoles. We show that Ura7, the major CTPS isoform in yeast, localizes to vacuoles under both nutrient-rich and starvation conditions. Genetic disruption of AP-3 function altered Ura7 assembly dynamics in starved cells, reducing total structures yet dramatically enhancing Ura7 cytoophidia elongation (∼five-fold), suggesting a dual regulatory role for AP-3 that both promotes Ura7 assembly and restrains elongation. Moreover, combining nutritional and pharmacological V-ATPase inhibition triggered massive Ura7 cytoophidia formation. These findings reveal a previously unrecognized spatial coupling between metabolic enzyme compartmentalization, vacuolar trafficking, and the pH regulation machinery, suggesting a new organizational principle whereby CTPS assembly dynamics respond to vacuolar function.

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Journal Article

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McCright M, Leih M, Nack A, Angers CG, Merz AJ, Odorizzi G

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