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Vol. 12, Issue 10, 3004-3015, October 2001




*U538 INSERM, CHU St-Antoine, 75571 Paris Cedex 12, France; and
Enzymes of the nucleotide pyrophosphatase/phosphodiesterase
(NPPase) family are expressed at opposite surfaces in polarized epithelial cells. We investigated the targeting signal of NPP1, which
is exclusively expressed at the basolateral surface. Full-length NPP1
and different constructs and mutants were transfected into the
polarized MDCK cell line. Expression of the proteins was analyzed by
confocal microscopy and surface biotinylation. The basolateral signal
of NPP1 was identified as a di-leucine motif located in the cytoplasmic
tail. Mutation of either or both leucines largely redirected NPP1 to
the apical surface. Furthermore, addition of the conserved sequence
AAASLLAP redirected the apical nucleotide pyrophosphatase/phosphodiesterase NPP3 to the basolateral surface. Full-length NPP1 was not significantly internalized. However, when the
cytoplasmic tail was deleted upstream the di-leucine motif or when the
six upstream flanking amino acids were deleted, the protein was mainly
found intracellularly. Endocytosis experiments indicated that these
mutants were endocytosed from the basolateral surface. These results
identify the basolateral signal of NPP1 as a short sequence including a
di-leucine motif that is dominant over apical determinants and point to
the importance of surrounding amino acids in determining whether the
signal will function as a basolateral signal only or as an endocytotic
signal as well.
Monash Medical School, Alfred Hospital, Prahran, Victoria
3181, Australia
Corresponding author. E-mail address:
maurice{at}st-antoine.inserm.fr
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