Rhodopsin trafficking and its role in retinal dystrophies.

TitleRhodopsin trafficking and its role in retinal dystrophies.
Publication TypeJournal Article
Year of Publication2000
AuthorsSung CH, Tai AW
JournalInt Rev Cytol
Volume195
Pagination215-67
Date Published2000
ISSN0074-7696
KeywordsAnimals, Carrier Proteins, Cell Survival, Cytoskeleton, Molecular Motor Proteins, Retinal Rod Photoreceptor Cells, Retinitis Pigmentosa, Rhodopsin
Abstract

We review the sorting/targeting steps involved in the delivery of rhodopsin to the outer segment compartment of highly polarized photoreceptor cells. The transport of rhodopsin includes (1) the sorting/budding of rhodopsin-containing vesicles at the trans-Golgi network, (2) the directional translocation of rhodopsin-bearing vesicles through the inner segment, and (3) the delivery of rhodopsin across the connecting cilium to the outer segment. Several independent lines of evidence suggest that the carboxyl-terminal, cytoplasmic tail of rhodopsin is involved in the post-Golgi trafficking of rhodopsin. Inappropriate subcellular targeting of naturally occurring rhodopsin mutants in vivo leads to photoreceptor cell death. Thus, the genes encoding mutations in the cellular components involved in photoreceptor protein transport are likely candidate genes for retinal dystrophies.

Alternate JournalInt. Rev. Cytol.
PubMed ID10603577
Grant ListR01 EY011307 / EY / NEI NIH HHS / United States