Abstract

In Saccharomyces cerevisiae, mitochondrial morphology changes when cells are shifted between nonfermentative and fermentative carbon sources. Here, we show that cells of S. cerevisiae grown in different glucose concentrations display different mitochondrial morphologies. The morphology of mitochondria in the cells growing in 0.5% glucose was similar to that of mitochondria in respiring cells. However, the mitochondria of cells growing in higher glucose concentrations (2% and 4%) became fragmented after growth in these media, due to the production of acetic acid; however, the fragmentation was not due to intracellular acidification. From a screen of mutants involved in sensing and utilizing nutrients, cells lacking TOR1 had reduced mitochondrial fragmentation, and autophagy was found to be essential for this reduction. Mitochondrial fragmentation in cells grown in high glucose was reversible by transferring them into conditioned medium from a culture grown on 0.5% glucose. Similarly, the chronological lifespan of cells grown in high glucose medium was reduced, and this phenotype could be reversed when cells were transferred to low glucose conditioned medium. These data indicate that chronological lifespan seems correlated with mitochondrial morphology of yeast cells and that both phenotypes can be influenced by factors from conditioned medium of cultures grown in low glucose medium.

Highlights

  • Mitochondria are important organelles whose primary function is to synthesize ATP, but they play important roles in many cellular processes including apoptosis and aging [1,2,3,4]

  • In order to determine whether increasing glucose concentration has an effect on mitochondrial structure and how this correlates with cellular lifespan in S. cerevisiae, we monitored the changes in mitochondrial morphology in S. cerevisiae cells growing in calorierestricted (0.5%) and high glucose conditions (2% and 4%)

  • Since nutrient availability might play a greater role than mitochondrial fission processes in modulating mitochondrial fragmentation when cells were grown at high glucose concentration, we examined mutant strains lacking genes involved in glucose sensing (SNF3, RGT2), glucose metabolism (HXK2, GPA2, PDE1, and PDE2), and general nutrient sensing (TOR1)

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Summary

Introduction

Mitochondria are important organelles whose primary function is to synthesize ATP, but they play important roles in many cellular processes including apoptosis and aging [1,2,3,4]. Due to their dynamic nature, the number and shape of mitochondria in a cell are variable depending on the growth conditions of the cell [5,6,7]. Very small mitochondria known as promitochondria are observed These are devoid of respiratory pigments and import ATP to perform the remaining essential metabolic functions [8]. High glucose concentrations promote calcium and mitogen protein kinase-mediated activation of mitochondrial fission and stimulate reactive oxygen species production [11]

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