LASS3 (longevity assurance homologue 3) is a mainly testis-specific (dihydro)ceramide synthase with relatively broad substrate specificity.
By Y. Mizutani, A. Kihara, Y. Igarashi. 2006
182 citations recorded by the source corpus.
Subfields: Biochemistry, Cell Biology, Molecular Biology
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In Biochemistry
- Michal Levy
- Yusuf A. Hannun
- S. Alexander
- Hannah Alexander
- A. Mesika
- J. Min
- M. Sivaguru
- P. V. Van Veldhoven
In Cell Biology
In Molecular Biology
Citations in the corpus
- Mammalian Ceramide Synthases (2010, background): “Interestingly, when human CerS5 was expressed in a yeast Dlag1Dlac1DLip1 mutant (71), it was able to synthesize C16-ceramides and the mutant survived in the absence of the C26-ceramides that are normally found in yeast.”
- An overview of sphingolipid metabolism: from synthesis to breakdown (2010, unknown): “water barrier in the epidermis [24], [25].”
- (Dihydro)ceramide Synthase 1–Regulated Sensitivity to Cisplatin Is Associated with the Activation of p38 Mitogen-Activated Protein Kinase and Is Abrogated by Sphingosine Kinase 1 (2007, background): “The mammalian enzymes have unique but greatly overlapping tissue distributions (21, 22, 28), but the precise roles of these enzymes and their unique products are not known.”
- Potentiation of cannabinoid-induced cytotoxicity in Mantle Cell Lymphoma through modulation of ceramide metabolism (2009, background): “CerS3 is regarded as a minor CerS that has mainly been described in skin and testis (10, 39) and has been shown to synthesize the longer ceramide”
- Differential expression of (dihydro)ceramide synthases in mouse brain: oligodendrocyte-specific expression of CerS2/Lass2 (2008, unknown): “Two other CerS, namely CerS3 and CerS4, have been reported to accept VLCFA-CoAs (>C18) as substrates (Riebeling et al. 2003; Mizutani et al. 2005, 2006).”
- Stress-induced ER to Golgi translocation of ceramide synthase 1 is dependent on proteasomal processing (2009, unknown): “The different CerS enzymes have unique patterns of tissue expression, implying transcriptional regulation in different tissues [9,13,14].”