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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2019
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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. |
format | Online Article Text |
id | pubmed-6602303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
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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