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Science 14 March 2003: Vol. 299. no. 5613, pp. 1740 - 1743 DOI: 10.1126/science.1080549
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Reports
Modulating Sphingolipid Biosynthetic Pathway Rescues Photoreceptor Degeneration
Usha Acharya,1*
Shetal Patel,1
Edmund Koundakjian,2
Kunio Nagashima,3
Xianlin Han,4
Jairaj K. Acharya1*
Mutations in proteins of the Drosophila
phototransduction cascade, a prototypic guanine
nucleotide-binding protein-coupled receptor signaling system,
lead to retinal degeneration and have been used as models to understand
human degenerative disorders. Here, modulating the sphingolipid
biosynthetic pathway rescued retinal degeneration in
Drosophila mutants. Targeted expression of
Drosophila neutral ceramidase rescued retinal degeneration in arrestin and phospholipase C mutants. Decreasing flux through the de
novo sphingolipid biosynthetic pathway also suppressed degeneration in
these mutants. Both genetic backgrounds modulated the endocytic
machinery because they suppressed defects in a dynamin mutant.
Suppression of degeneration in arrestin mutant flies expressing ceramidase correlated with a decrease in ceramide levels. Thus, enzymes
of sphingolipid metabolism may be suitable targets in the therapeutic
management of retinal degeneration.
1 Regulation of Cell Growth Laboratory,
National Cancer Institute-Frederick, Frederick, MD 21702, USA.
2 Howard Hughes Medical Institute, University of
California, San Diego, La Jolla, CA 92093, USA.
3
Electron Microscopy Facility/Image Analysis Laboratory, Science
Applications International Corporation, Frederick, MD 21702, USA.
4 Division of Bioorganic Chemistry and Molecular
Pharmacology, Department of Medicine, Washington University School of
Medicine, St. Louis, MO 63110, USA.
*
To whom correspondence should be addressed. E-mail:
acharyaj{at}mail.ncifcrf.gov (J.K.A.),
acharyau{at}mail.ncifcrf.gov (U.A.)
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- Y. Yoshimura, M. Tani, N. Okino, H. Iida, and M. Ito (2004)
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