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Vol. 13, Issue 12, 4206-4220, December 2002
The Ronald O. Perelman Department of Dermatology and the Department
of Cell Biology, New York University School of Medicine, New York, New
York 10016
Mutations in the mouse p (pink-eyed dilution) and
human P genes lead to melanosomal defects and ocular
developmental abnormalities. Despite the critical role played by the p
gene product in controlling tyrosinase processing and melanosome
biogenesis, its precise biological function is still not defined. We
have expressed p heterologously in the yeast Saccharomyces
cerevisiae to study its function in greater detail.
Immunofluorescence studies revealed that p reaches the yeast vacuolar
membrane via the prevacuolar compartment. Yeast cells expressing p
exhibited increased sensitivity to a number of toxic compounds,
including arsenicals. Similarly, cultured murine melanocytes expressing
a functional p gene were also found to be more sensitive
to arsenical compounds compared with p-null cell lines. Intracellular
glutathione, known to play a role in detoxification of arsenicals, was
diminished by 50% in p-expressing yeast. By using the
glutathione-conjugating dye monochlorobimane, in combination with
acivicin, an inhibitor of vacuolar gamma-glutamyl cysteine
transpeptidase, involved in the breakdown of glutathione, we found that
p facilitates the vacuolar accumulation of glutathione. Our data
demonstrate that the pink-eyed dilution protein increases cellular
sensitivity to arsenicals and other metalloids and can modulate
intracellular glutathione metabolism.
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