Abstract

BackgroundSaccharomyces cerevisiae ScGdt1 and mammalian TMEM165 are two members of the UPF0016 membrane protein family that is likely to form a new group of Ca2+/H+ antiporter and/or a Mn2+ transporter in the Golgi apparatus. We have previously shown that Candida albicans CaGDT1 is a functional ortholog of ScGDT1 in the response of S. cerevisiae to calcium stress. However, how CaGdt1 together with the Golgi calcium pump CaPmr1 regulate calcium homeostasis and cell wall integrity in this fungal pathogen remains unknown.MethodsChemical sensitivity was tested by dilution assay. Cell survival was examined by measuring colony-forming units and staining with Annexin V-FITC and propidium iodide. Calcium signaling was examined by expression of downstream target gene CaUTR2, while cell wall integrity signaling was revealed by detection of phosphorylated Mkc1 and Cek1. Subcellular localization of CaGdt1 was examined through direct and indirect immunofluorescent approaches. Transcriptomic analysis was carried out with RNA sequencing.ResultsThis study shows that Candida albicans CaGDT1 is also a functional ortholog of ScGDT1 in the response of S. cerevisiae to cell wall stress. CaGdt1 is localized in the Golgi apparatus but at distinct sites from CaPmr1 in C. albicans. Loss of CaGDT1 increases the sensitivity of cell lacking CaPMR1 to cell wall and ER stresses. Deletion of CaGDT1 and/or CaPMR1 increases calcium uptake and activates the calcium/calcineurin signaling. Transcriptomic profiling reveals that core functions shared by CaGdt1 and CaPmr1 are involved in the regulation of cellular transport of metal ions and amino acids. However, CaGdt1 has distinct functions from CaPmr1. Chitin synthase gene CHS2 is up regulated in all three mutants, while CHS3 is only up regulated in the pmr1/pmr1 and the gdt1/gdt1 pmr1/pmr1 mutants. Five genes (DIE2, STT3, OST3, PMT1 and PMT4) of glycosylation pathway and one gene (SWI4) of the cell wall integrity (CWI) pathway are upregulated due to deletion of CaGDT1 and/or CaPMR1. Consistently, deletion of either CaPMR1 or CaGDT1 activates the CaCek1-mediated CWI signaling in a cell wall stress-independent fashion. Calcineurin function is required for the integrity of the cell wall and vacuolar compartments of cells lacking both GDT1 and CaPMR1.ConclusionsCaPmr1 is the major player in the regulation of calcium homeostasis and cell wall stress, while CaGdt1 plays a compensatory role for CaPmr1 in the Golgi compartment in C. albicans.

Highlights

  • Saccharomyces cerevisiae ScGdt1 and mammalian transmembrane protein 165 (TMEM165) are two members of the uncharacterized protein family UPF0016 (UPF0016) membrane protein family that is likely to form a new group of Ca2+/H+ antiporter and/or a Mn2+ transporter in the Golgi apparatus

  • This study provides evidence that the functional ortholog of ScGdt1, Candida albicans CaGdt1 plays a compensatory role for CaPmr1, the Ca2+/Mn2+ ATPase that is required for Ca2+ and Mn2+ transport into the Golgi and involved in Ca2+ dependent protein sorting processing

  • S. cerevisiae cells lacking ScGDT1 were not sensitive to 5 mM EGTA, 0.4 M CaCl2, 100 μg ml− 1 Congo red (CR) and 50 μg ml− 1 Calcofluor white (CFW) [7], we found that deletion of ScGDT1 increased the sensitivity of cells lacking ScPMR1 to all these reagents (Additional file 1: Figure S1A)

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Summary

Introduction

Saccharomyces cerevisiae ScGdt and mammalian TMEM165 are two members of the UPF0016 membrane protein family that is likely to form a new group of Ca2+/H+ antiporter and/or a Mn2+ transporter in the Golgi apparatus. We have previously shown that Candida albicans CaGDT1 is a functional ortholog of ScGDT1 in the response of S. cerevisiae to calcium stress. How CaGdt together with the Golgi calcium pump CaPmr regulate calcium homeostasis and cell wall integrity in this fungal pathogen remains unknown. Functional counterparts of yeast calcium channels, pumps and exchangers exist and function in similar fashions in mammalian cells [2]. In Saccharomyces cerevisiae, calcium homeostasis is regulated through calcium transporters and sequestrates in the plasma and organelle membranes [2,3,4]. Rch is a novel negative regulator of calcium uptake in the plasma membrane of S. cerevisiae and C. albicans [12,13,14,15]

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