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The Journal of Neuroscience, October 1, 1999, 19(19):8435-8442
Drosophila presenilin Is Required for
Neuronal Differentiation and Affects Notch Subcellular Localization and
Signaling
Yiquan
Guo1,
Izhar
Livne-Bar1,
Lily
Zhou1, and
Gabrielle L.
Boulianne1, 2
1 Program in Developmental Biology, Hospital for Sick
Children, Toronto, Ontario, Canada M5G 1X8, and
2 Department of Medical Genetics and Zoology, University of
Toronto, Toronto, Ontario, Canada
Presenilins are a highly conserved family of proteins first
identified as causative genes in early onset familial Alzheimer's disease. Recent studies have suggested a role for presenilins in the
Notch-signaling pathway, but their specific function within this
pathway remains unclear. Here, we have characterized the Drosophila presenilin gene and protein and studied their
interaction with Notch in both mutants and transgenics. We find that
the Drosophila presenilin protein is proteolytically
cleaved and broadly expressed during development with the highest
levels in neurons within the larval CNS. We also show that
mutations in Drosophila presenilin (Dps)
genetically interact with Notch and result in an early pupal-lethal phenotype characterized by defects in eye and wing development and
incomplete neuronal differentiation within the larval CNS. Moreover, we
find that processing of Notch in the Golgi by the furin protease is
unaffected in Dps mutants and that Notch is present and may even
accumulate on the plasma membrane of neuroblasts in the larval CNS of
Dps mutants. In contrast, overexpression of Dps in
transgenics causes Notch to accumulate in the cytoplasm. Taken
together, these results indicate that Drosophila
presenilin is required for proper neuronal differentiation and may
regulate the subcellular localization of Notch proteins within cells,
necessary for their accumulation and subsequent signaling capabilities.
Key words:
Drosophila; presenilin; Notch; localization; Delta; neurogenesis
Copyright © 1999 Society for Neuroscience 0270-6474/99/19198435-08$05.00/0
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