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Identification of a modulator of the actin cytoskeleton, mitochondria, nutrient metabolism and lifespan in yeast

In yeast, actin cables are F-actin bundles that are essential for cell division through their function as tracks for cargo movement from mother to daughter cell. Actin cables also affect yeast lifespan by promoting transport and inheritance of higher-functioning mitochondria to daughter cells. Here,...

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Autores principales: Sing, Cierra N., Garcia, Enrique J., Lipkin, Thomas G., Huckaba, Thomas M., Tsang, Catherine A., Coughlin, Arielle C., Yang, Emily J., Boldogh, Istvan R., Higuchi-Sanabria, Ryo, Pon, Liza A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110415/
https://www.ncbi.nlm.nih.gov/pubmed/35577788
http://dx.doi.org/10.1038/s41467-022-30045-9
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author Sing, Cierra N.
Garcia, Enrique J.
Lipkin, Thomas G.
Huckaba, Thomas M.
Tsang, Catherine A.
Coughlin, Arielle C.
Yang, Emily J.
Boldogh, Istvan R.
Higuchi-Sanabria, Ryo
Pon, Liza A.
author_facet Sing, Cierra N.
Garcia, Enrique J.
Lipkin, Thomas G.
Huckaba, Thomas M.
Tsang, Catherine A.
Coughlin, Arielle C.
Yang, Emily J.
Boldogh, Istvan R.
Higuchi-Sanabria, Ryo
Pon, Liza A.
author_sort Sing, Cierra N.
collection PubMed
description In yeast, actin cables are F-actin bundles that are essential for cell division through their function as tracks for cargo movement from mother to daughter cell. Actin cables also affect yeast lifespan by promoting transport and inheritance of higher-functioning mitochondria to daughter cells. Here, we report that actin cable stability declines with age. Our genome-wide screen for genes that affect actin cable stability identified the open reading frame YKL075C. Deletion of YKL075C results in increases in actin cable stability and abundance, mitochondrial fitness, and replicative lifespan. Transcriptome analysis revealed a role for YKL075C in regulating branched-chain amino acid (BCAA) metabolism. Consistent with this, modulation of BCAA metabolism or decreasing leucine levels promotes actin cable stability and function in mitochondrial quality control. Our studies support a role for actin stability in yeast lifespan, and demonstrate that this process is controlled by BCAA and a previously uncharacterized ORF YKL075C, which we refer to as actin, aging and nutrient modulator protein 1 (AAN1).
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spelling pubmed-91104152022-05-18 Identification of a modulator of the actin cytoskeleton, mitochondria, nutrient metabolism and lifespan in yeast Sing, Cierra N. Garcia, Enrique J. Lipkin, Thomas G. Huckaba, Thomas M. Tsang, Catherine A. Coughlin, Arielle C. Yang, Emily J. Boldogh, Istvan R. Higuchi-Sanabria, Ryo Pon, Liza A. Nat Commun Article In yeast, actin cables are F-actin bundles that are essential for cell division through their function as tracks for cargo movement from mother to daughter cell. Actin cables also affect yeast lifespan by promoting transport and inheritance of higher-functioning mitochondria to daughter cells. Here, we report that actin cable stability declines with age. Our genome-wide screen for genes that affect actin cable stability identified the open reading frame YKL075C. Deletion of YKL075C results in increases in actin cable stability and abundance, mitochondrial fitness, and replicative lifespan. Transcriptome analysis revealed a role for YKL075C in regulating branched-chain amino acid (BCAA) metabolism. Consistent with this, modulation of BCAA metabolism or decreasing leucine levels promotes actin cable stability and function in mitochondrial quality control. Our studies support a role for actin stability in yeast lifespan, and demonstrate that this process is controlled by BCAA and a previously uncharacterized ORF YKL075C, which we refer to as actin, aging and nutrient modulator protein 1 (AAN1). Nature Publishing Group UK 2022-05-16 /pmc/articles/PMC9110415/ /pubmed/35577788 http://dx.doi.org/10.1038/s41467-022-30045-9 Text en © The Author(s) 2022 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
Sing, Cierra N.
Garcia, Enrique J.
Lipkin, Thomas G.
Huckaba, Thomas M.
Tsang, Catherine A.
Coughlin, Arielle C.
Yang, Emily J.
Boldogh, Istvan R.
Higuchi-Sanabria, Ryo
Pon, Liza A.
Identification of a modulator of the actin cytoskeleton, mitochondria, nutrient metabolism and lifespan in yeast
title Identification of a modulator of the actin cytoskeleton, mitochondria, nutrient metabolism and lifespan in yeast
title_full Identification of a modulator of the actin cytoskeleton, mitochondria, nutrient metabolism and lifespan in yeast
title_fullStr Identification of a modulator of the actin cytoskeleton, mitochondria, nutrient metabolism and lifespan in yeast
title_full_unstemmed Identification of a modulator of the actin cytoskeleton, mitochondria, nutrient metabolism and lifespan in yeast
title_short Identification of a modulator of the actin cytoskeleton, mitochondria, nutrient metabolism and lifespan in yeast
title_sort identification of a modulator of the actin cytoskeleton, mitochondria, nutrient metabolism and lifespan in yeast
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110415/
https://www.ncbi.nlm.nih.gov/pubmed/35577788
http://dx.doi.org/10.1038/s41467-022-30045-9
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