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Fig. 2. Sply encodes the Drosophila sphingosine-1-phosphate
lyase. (A) CLUSTALW alignment of Sply. The predicted protein product of
Sply is 49% and 43% identical and 68% and 60% similar to human and
yeast SPL protein sequences respectively. The broken line indicates the
putative transmembrane region. The unbroken line indicates a consensus
pyridoxal phosphate-binding motif. (B) Sply gene organization. Open
reading frames GH13783 and LP04413 and location of transposon insertion
(P{PZ}Sply05091) are indicated. (C) Overexpression of Sply
in a Saccharomyces cerevisiae SPL mutant restores sphingosine
resistance. The LP04413 and GH13783 cDNAs were cloned into yeast expression
vector pYES2 and transformed into a yeast SPL mutant strain (dpl1),
as described in the Materials and Methods. The transformed strain
(dpl1 + Sply) was compared with wild type (DPL1)
and SPL mutant overexpressing endogenous yeast SPL (dpl1 +
DPL1) strains in a sphingosine resistance assay. Dilutions of
saturated cultures for each strain are indicated above. (D) Expression of
Sply in a Saccharomyces cerevisiae SPL mutant restores SPL
enzyme activity. Whole cell extracts of Saccharomyces cerevisiae wild
type, SPL mutant (dpl1) and SPL mutant overexpressing Sply
(dpl1 + Sply) strains were analyzed for SPL activity.