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Regulation of Sphingolipid Biosynthesis by the Morphogenesis Checkpoint Kinase Swe1

Sphingolipid (SL) biosynthesis is negatively regulated by the highly conserved endoplasmic reticulum-localized Orm family proteins. Defective SL synthesis in Saccharomyces cerevisiae leads to increased phosphorylation and inhibition of Orm proteins by the kinase Ypk1. Here we present evidence that t...

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Autores principales: Chauhan, Neha, Han, Gongshe, Somashekarappa, Niranjanakumari, Gable, Kenneth, Dunn, Teresa, Kohlwein, Sepp D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4732232/
https://www.ncbi.nlm.nih.gov/pubmed/26634277
http://dx.doi.org/10.1074/jbc.M115.693200
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author Chauhan, Neha
Han, Gongshe
Somashekarappa, Niranjanakumari
Gable, Kenneth
Dunn, Teresa
Kohlwein, Sepp D.
author_facet Chauhan, Neha
Han, Gongshe
Somashekarappa, Niranjanakumari
Gable, Kenneth
Dunn, Teresa
Kohlwein, Sepp D.
author_sort Chauhan, Neha
collection PubMed
description Sphingolipid (SL) biosynthesis is negatively regulated by the highly conserved endoplasmic reticulum-localized Orm family proteins. Defective SL synthesis in Saccharomyces cerevisiae leads to increased phosphorylation and inhibition of Orm proteins by the kinase Ypk1. Here we present evidence that the yeast morphogenesis checkpoint kinase, Swe1, regulates SL biosynthesis independent of the Ypk1 pathway. Deletion of the Swe1 kinase renders mutant cells sensitive to serine palmitoyltransferase inhibition due to impaired sphingoid long-chain base synthesis. Based on these data and previous results, we suggest that Swe1 kinase perceives alterations in SL homeostasis, activates SL synthesis, and may thus represent the missing regulatory link that controls the SL rheostat during the cell cycle.
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spelling pubmed-47322322016-02-09 Regulation of Sphingolipid Biosynthesis by the Morphogenesis Checkpoint Kinase Swe1 Chauhan, Neha Han, Gongshe Somashekarappa, Niranjanakumari Gable, Kenneth Dunn, Teresa Kohlwein, Sepp D. J Biol Chem Lipids Sphingolipid (SL) biosynthesis is negatively regulated by the highly conserved endoplasmic reticulum-localized Orm family proteins. Defective SL synthesis in Saccharomyces cerevisiae leads to increased phosphorylation and inhibition of Orm proteins by the kinase Ypk1. Here we present evidence that the yeast morphogenesis checkpoint kinase, Swe1, regulates SL biosynthesis independent of the Ypk1 pathway. Deletion of the Swe1 kinase renders mutant cells sensitive to serine palmitoyltransferase inhibition due to impaired sphingoid long-chain base synthesis. Based on these data and previous results, we suggest that Swe1 kinase perceives alterations in SL homeostasis, activates SL synthesis, and may thus represent the missing regulatory link that controls the SL rheostat during the cell cycle. American Society for Biochemistry and Molecular Biology 2016-01-29 2015-12-03 /pmc/articles/PMC4732232/ /pubmed/26634277 http://dx.doi.org/10.1074/jbc.M115.693200 Text en © 2016 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version free via Creative Commons CC-BY license (http://creativecommons.org/licenses/by/4.0) .
spellingShingle Lipids
Chauhan, Neha
Han, Gongshe
Somashekarappa, Niranjanakumari
Gable, Kenneth
Dunn, Teresa
Kohlwein, Sepp D.
Regulation of Sphingolipid Biosynthesis by the Morphogenesis Checkpoint Kinase Swe1
title Regulation of Sphingolipid Biosynthesis by the Morphogenesis Checkpoint Kinase Swe1
title_full Regulation of Sphingolipid Biosynthesis by the Morphogenesis Checkpoint Kinase Swe1
title_fullStr Regulation of Sphingolipid Biosynthesis by the Morphogenesis Checkpoint Kinase Swe1
title_full_unstemmed Regulation of Sphingolipid Biosynthesis by the Morphogenesis Checkpoint Kinase Swe1
title_short Regulation of Sphingolipid Biosynthesis by the Morphogenesis Checkpoint Kinase Swe1
title_sort regulation of sphingolipid biosynthesis by the morphogenesis checkpoint kinase swe1
topic Lipids
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4732232/
https://www.ncbi.nlm.nih.gov/pubmed/26634277
http://dx.doi.org/10.1074/jbc.M115.693200
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