Disruption of the ceramide synthase LOH1 causes spontaneous cell death in Arabidopsis thaliana

2011 | journal article. A publication with affiliation to the University of Göttingen.

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​Disruption of the ceramide synthase LOH1 causes spontaneous cell death in Arabidopsis thaliana​
Ternes, P.; Feussner, K.; Werner, S.; Lerche, J.; Iven, T.; Heilmann, I. & Riezman, H. et al.​ (2011) 
New Phytologist192(4) pp. 841​-854​.​ DOI: https://doi.org/10.1111/j.1469-8137.2011.03852.x 

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Authors
Ternes, Philipp; Feussner, Kirstin; Werner, Stephanie; Lerche, Jennifer; Iven, Tim; Heilmann, Ingo; Riezman, Howard; Feussner, Ivo
Abstract
The bioactive lipid ceramide is produced by the enzyme ceramide synthase, which exists in several isoforms in most eukaryotic organisms. Here, we investigated functional differences between the three ceramide synthase isoforms in Arabidopsis thaliana. The biochemical properties of the three ceramide synthases were investigated by comparing lipid profiles of yeast strains expressing LOH1, LOH2 or LOH3 with those of wild-type and loh1, loh2 and loh3 knockout plants. Expression profiles of the ceramide synthases and of the pathogenesis-related gene PR-1 were investigated by real-time PCR. Each ceramide synthase isoform showed a characteristic preference regarding acyl-CoA chain length as well as sphingoid base hydroxylation, which matches the pattern of ceramide and glucosylceramide species found in leaves. After extended culture under short-day conditions, loh1 plants showed spontaneous cell death accompanied by enhanced expression of PR-1. The levels of free trihydroxy sphingoid bases as well as ceramide and glucosylceramide species with C(16) fatty acid were significantly elevated while species with C(20)-C(28) fatty acids were reduced. These data suggest that spontaneous cell death in the loh1 line is triggered either by the accumulation of free trihydroxy sphingoid bases or ceramide species with C(16) fatty acid.
Issue Date
2011
Status
published
Publisher
Wiley-blackwell
Journal
New Phytologist 
ISSN
0028-646X

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