TY - JOUR
T1 - Yeast ceramide synthases, Lag1 and Lac1, have distinct substrate specificity
AU - Megyeri, Marton
AU - Prasad, Rupali
AU - Volpert, Giora
AU - Sliwa-Gonzalez, Andrzej
AU - Haribowo, A. Galih
AU - Aguilera-Romero, Auxiliadora
AU - Riezman, Howard
AU - Barral, Yves
AU - Futerman, Anthony H.
AU - Schuldiner, Maya
N1 - M.S., A.G., H.R. and M.M. were supported by an EU ITN Seventh Framework Programme ‘Sphingonet’. A.G. was supported by Institute of Genetics and Genomics of Geneva (iGE3). H.R. was supported by the NCCR Chemical Biology and the Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung. Y.B., R.P. and A.S.-G. were supported by an advanced grant from the European Research Council and A.S.-G. by a PhD grant from the Eidgenössische Technische Hochschule Zürich. Work in the Schuldiner lab is supported by a Volkswagen Foundation ‘Life’ grant (number 93092) and by a BARD grant (number US-5029-17). A.H.F. is the Joseph Meyerhoff Professor of Biochemistry at the Weizmann Institute of Science. M.S. is an Incumbent of the Dr Gilbert Omenn and Martha Darling Professorial Chair in Molecular Genetics. Deposited in PMC for immediate release. Conceptualization: M.M., H.R., Y.B., A.H.F., M.S.; Methodology: M.M.; Validation: M.M.; Formal analysis: M.M., A.H.F., M.S.; Investigation: M.M., R.P., G.V., A.S.-G., A.G., A.A.-R.; Resources: Y.B., A.H.F., M.S.; Data curation: R.P., A.G.; Writing - original draft: M.M., A.H.F., M.S.; Writing - review & editing: M.M., R.P., G.V., A.S.-G., A.G., A.A.-R., H.R., Y.B., A.H.F., M.S.; Visualization: M.M.; Supervision: H.R., Y.B., A.H.F., M.S.; Project administration: A.H.F., M.S.; Funding acquisition: H.R., Y.B., A.H.F., M.S.
PY - 2019/6/24
Y1 - 2019/6/24
N2 - 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 Delta lag1 cells have an increased lifespan while Delta lac1 cells do not.
AB - 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 Delta lag1 cells have an increased lifespan while Delta lac1 cells do not.
UR - http://www.scopus.com/inward/record.url?scp=85068216651&partnerID=8YFLogxK
U2 - 10.1242/jcs.228411
DO - 10.1242/jcs.228411
M3 - مقالة
SN - 0021-9533
VL - 132
JO - Journal of Cell Science
JF - Journal of Cell Science
M1 - jcs228411
ER -