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Yeast ceramide synthases, Lag1 and Lac1, have distinct substrate specificity

LAG1 was the first longevity assurance gene discovered in Saccharomyces cerevisiae. The Lag1 protein is a ceramide synthase and its homolog, Lac1, has a similar enzymatic function but no role in aging. Lag1 and Lac1 lie in an enzymatic branch point of the sphingolipid pathway that is interconnected...

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Autores principales: Megyeri, Márton, Prasad, Rupali, Volpert, Giora, Sliwa-Gonzalez, Andrzej, Haribowo, A. Galih, Aguilera-Romero, Auxiliadora, Riezman, Howard, Barral, Yves, Futerman, Anthony H., Schuldiner, Maya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602303/
https://www.ncbi.nlm.nih.gov/pubmed/31164445
http://dx.doi.org/10.1242/jcs.228411
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author Megyeri, Márton
Prasad, Rupali
Volpert, Giora
Sliwa-Gonzalez, Andrzej
Haribowo, A. Galih
Aguilera-Romero, Auxiliadora
Riezman, Howard
Barral, Yves
Futerman, Anthony H.
Schuldiner, Maya
author_facet Megyeri, Márton
Prasad, Rupali
Volpert, Giora
Sliwa-Gonzalez, Andrzej
Haribowo, A. Galih
Aguilera-Romero, Auxiliadora
Riezman, Howard
Barral, Yves
Futerman, Anthony H.
Schuldiner, Maya
author_sort Megyeri, Márton
collection PubMed
description LAG1 was the first longevity assurance gene discovered in Saccharomyces cerevisiae. The Lag1 protein is a ceramide synthase and its homolog, Lac1, has a similar enzymatic function but no role in aging. Lag1 and Lac1 lie in an enzymatic branch point of the sphingolipid pathway that is interconnected by the activity of the C4 hydroxylase, Sur2. By uncoupling the enzymatic branch point and using lipidomic mass spectrometry, metabolic labeling and in vitro assays we show that Lag1 preferentially synthesizes phyto-sphingolipids. Using photo-bleaching experiments we show that Lag1 is uniquely required for the establishment of a lateral diffusion barrier in the nuclear envelope, which depends on phytoceramide. Given the role of this diffusion barrier in the retention of aging factors in the mother cell, we suggest that the different specificities of the two ceramide synthases, and the specific effect of Lag1 on asymmetrical inheritance, may explain why Δlag1 cells have an increased lifespan while Δlac1 cells do not.
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spelling pubmed-66023032019-07-16 Yeast ceramide synthases, Lag1 and Lac1, have distinct substrate specificity Megyeri, Márton Prasad, Rupali Volpert, Giora Sliwa-Gonzalez, Andrzej Haribowo, A. Galih Aguilera-Romero, Auxiliadora Riezman, Howard Barral, Yves Futerman, Anthony H. Schuldiner, Maya J Cell Sci Research Article LAG1 was the first longevity assurance gene discovered in Saccharomyces cerevisiae. The Lag1 protein is a ceramide synthase and its homolog, Lac1, has a similar enzymatic function but no role in aging. Lag1 and Lac1 lie in an enzymatic branch point of the sphingolipid pathway that is interconnected by the activity of the C4 hydroxylase, Sur2. By uncoupling the enzymatic branch point and using lipidomic mass spectrometry, metabolic labeling and in vitro assays we show that Lag1 preferentially synthesizes phyto-sphingolipids. Using photo-bleaching experiments we show that Lag1 is uniquely required for the establishment of a lateral diffusion barrier in the nuclear envelope, which depends on phytoceramide. Given the role of this diffusion barrier in the retention of aging factors in the mother cell, we suggest that the different specificities of the two ceramide synthases, and the specific effect of Lag1 on asymmetrical inheritance, may explain why Δlag1 cells have an increased lifespan while Δlac1 cells do not. The Company of Biologists Ltd 2019-06-15 2019-06-24 /pmc/articles/PMC6602303/ /pubmed/31164445 http://dx.doi.org/10.1242/jcs.228411 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Megyeri, Márton
Prasad, Rupali
Volpert, Giora
Sliwa-Gonzalez, Andrzej
Haribowo, A. Galih
Aguilera-Romero, Auxiliadora
Riezman, Howard
Barral, Yves
Futerman, Anthony H.
Schuldiner, Maya
Yeast ceramide synthases, Lag1 and Lac1, have distinct substrate specificity
title Yeast ceramide synthases, Lag1 and Lac1, have distinct substrate specificity
title_full Yeast ceramide synthases, Lag1 and Lac1, have distinct substrate specificity
title_fullStr Yeast ceramide synthases, Lag1 and Lac1, have distinct substrate specificity
title_full_unstemmed Yeast ceramide synthases, Lag1 and Lac1, have distinct substrate specificity
title_short Yeast ceramide synthases, Lag1 and Lac1, have distinct substrate specificity
title_sort yeast ceramide synthases, lag1 and lac1, have distinct substrate specificity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602303/
https://www.ncbi.nlm.nih.gov/pubmed/31164445
http://dx.doi.org/10.1242/jcs.228411
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