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Cell cycle-linked vacuolar pH dynamics regulate amino acid homeostasis and cell growth

Amino acid homeostasis is critical for many cellular processes. It is well established that amino acids are compartmentalized using pH gradients generated between organelles and the cytoplasm; however, the dynamics of this partitioning has not been explored. Here we develop a highly sensitive pH rep...

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Autores principales: Okreglak, Voytek, Ling, Rachel, Ingaramo, Maria, Thayer, Nathaniel H., Millett-Sikking, Alfred, Gottschling, Daniel E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10590757/
https://www.ncbi.nlm.nih.gov/pubmed/37640943
http://dx.doi.org/10.1038/s42255-023-00872-1
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author Okreglak, Voytek
Ling, Rachel
Ingaramo, Maria
Thayer, Nathaniel H.
Millett-Sikking, Alfred
Gottschling, Daniel E.
author_facet Okreglak, Voytek
Ling, Rachel
Ingaramo, Maria
Thayer, Nathaniel H.
Millett-Sikking, Alfred
Gottschling, Daniel E.
author_sort Okreglak, Voytek
collection PubMed
description Amino acid homeostasis is critical for many cellular processes. It is well established that amino acids are compartmentalized using pH gradients generated between organelles and the cytoplasm; however, the dynamics of this partitioning has not been explored. Here we develop a highly sensitive pH reporter and find that the major amino acid storage compartment in Saccharomyces cerevisiae, the lysosome-like vacuole, alkalinizes before cell division and re-acidifies as cells divide. The vacuolar pH dynamics require the uptake of extracellular amino acids and activity of TORC1, the v-ATPase and the cycling of the vacuolar specific lipid phosphatidylinositol 3,5-bisphosphate, which is regulated by the cyclin-dependent kinase Pho85 (CDK5 in mammals). Vacuolar pH regulation enables amino acid sequestration and mobilization from the organelle, which is important for mitochondrial function, ribosome homeostasis and cell size control. Collectively, our data provide a new paradigm for the use of dynamic pH-dependent amino acid compartmentalization during cell growth/division.
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spelling pubmed-105907572023-10-24 Cell cycle-linked vacuolar pH dynamics regulate amino acid homeostasis and cell growth Okreglak, Voytek Ling, Rachel Ingaramo, Maria Thayer, Nathaniel H. Millett-Sikking, Alfred Gottschling, Daniel E. Nat Metab Article Amino acid homeostasis is critical for many cellular processes. It is well established that amino acids are compartmentalized using pH gradients generated between organelles and the cytoplasm; however, the dynamics of this partitioning has not been explored. Here we develop a highly sensitive pH reporter and find that the major amino acid storage compartment in Saccharomyces cerevisiae, the lysosome-like vacuole, alkalinizes before cell division and re-acidifies as cells divide. The vacuolar pH dynamics require the uptake of extracellular amino acids and activity of TORC1, the v-ATPase and the cycling of the vacuolar specific lipid phosphatidylinositol 3,5-bisphosphate, which is regulated by the cyclin-dependent kinase Pho85 (CDK5 in mammals). Vacuolar pH regulation enables amino acid sequestration and mobilization from the organelle, which is important for mitochondrial function, ribosome homeostasis and cell size control. Collectively, our data provide a new paradigm for the use of dynamic pH-dependent amino acid compartmentalization during cell growth/division. Nature Publishing Group UK 2023-08-28 2023 /pmc/articles/PMC10590757/ /pubmed/37640943 http://dx.doi.org/10.1038/s42255-023-00872-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Okreglak, Voytek
Ling, Rachel
Ingaramo, Maria
Thayer, Nathaniel H.
Millett-Sikking, Alfred
Gottschling, Daniel E.
Cell cycle-linked vacuolar pH dynamics regulate amino acid homeostasis and cell growth
title Cell cycle-linked vacuolar pH dynamics regulate amino acid homeostasis and cell growth
title_full Cell cycle-linked vacuolar pH dynamics regulate amino acid homeostasis and cell growth
title_fullStr Cell cycle-linked vacuolar pH dynamics regulate amino acid homeostasis and cell growth
title_full_unstemmed Cell cycle-linked vacuolar pH dynamics regulate amino acid homeostasis and cell growth
title_short Cell cycle-linked vacuolar pH dynamics regulate amino acid homeostasis and cell growth
title_sort cell cycle-linked vacuolar ph dynamics regulate amino acid homeostasis and cell growth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10590757/
https://www.ncbi.nlm.nih.gov/pubmed/37640943
http://dx.doi.org/10.1038/s42255-023-00872-1
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