Abstract

Seeking to better understand how membrane trafficking is coordinated with phospholipid synthesis in yeast, we investigated lipid synthesis in several Sec(-) temperature-sensitive mutants, including sec13-1. Upon shift of sec13-1 cells to the restrictive temperature of 37 degrees C, phospholipid synthesis decreased dramatically relative to the wild type control, whereas synthesis of neutral lipids, especially triacylglycerol (TAG), increased. When examined by fluorescence microscopy, the number of lipid droplets appeared to increase and formed aggregates in sec13-1 cells shifted to 37 degrees C. Electron microscopy confirmed the increase in lipid droplet number and revealed that many were associated with the vacuole. Analysis of lipid metabolism in strains lacking TAG synthase genes demonstrated that the activities of the products of these genes contribute to accumulation of TAG in sec13-1 cells after the shift to 37 degrees C. Furthermore, the permissive temperature for growth of the sec13-1 strain lacking TAG synthase genes was 3 degrees C lower than sec13-1 on several different growth media, indicating that the synthesis of TAG has physiological significance under conditions of secretory stress. Together these results suggest that following a block in membrane trafficking, yeast cells channel lipid metabolism from phospholipid synthesis into synthesis of TAG and other neutral lipids to form lipid droplets. We conclude that this metabolic switch provides a degree of protection to cells during secretory stress.

Highlights

  • 2 The abbreviations used are: ER, endoplasmic reticulum; TAG, triacylglycerol; DAG, diacylglycerol; PA, phosphatidic acid; PI, phosphatidylinositol; PS, phosphatidylserine; PC, phosphatidylcholine; PE, phosphatidylethanolamine; UPR, unfolded protein response; cytidine diphosphate-diacylglycerol (CDP-DAG), cytidine diphosphatediacylglycerol; YPD, yeast extract/peptone/dextrose; TPL, total 32P associated with the sum of the following phospholipids: PA, PI, PS, PE, PC; FACS, fluorescence-activated cell sorter; PBS, phosphate-buffered saline; Carboxypeptidase Y (CPY), carboxypeptidase Y

  • Tute the entire endomembrane system. Following their synthesis and insertion into the ER, proteins destined for the secretory pathway are folded and sorted into COPII vesicles that are delivered to their ultimate cellular locations via cellular membrane trafficking pathways

  • Seeking to better understand how membrane trafficking pathways are coordinated with phospholipid synthesis, we investigated the status of membrane lipid synthesis in several SecϪ mutants, including sec13-1, shifted to restrictive growth conditions

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Summary

List of yeast strains used in this study

MATa sec his leu ura MAT␣ sec13-1his ura leu MAT␣ lro1⌬::HIS3 his leu ura MAT␣ dga1⌬::kanMX his leu ura MAT␣ lro1⌬::HIS3 dga1⌬:: kanMX his.

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EXPERIMENTAL PROCEDURES
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