HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Targeting of Drosophila rhodopsin requires helix 8 but not the distal C-terminus.

AbstractBACKGROUND:
The fundamental role of the light receptor rhodopsin in visual function and photoreceptor cell development has been widely studied. Proper trafficking of rhodopsin to the photoreceptor membrane is of great importance. In human, mutations in rhodopsin involving its intracellular mislocalization, are the most frequent cause of autosomal dominant Retinitis Pigmentosa, a degenerative retinal pathology characterized by progressive blindness. Drosophila is widely used as an animal model in visual and retinal degeneration research. So far, little is known about the requirements for proper rhodopsin targeting in Drosophila.
METHODOLOGY/PRINCIPAL FINDINGS:
Different truncated fly-rhodopsin Rh1 variants were expressed in the eyes of Drosophila and their localization was analyzed in vivo or by immunofluorescence. A mutant lacking the last 23 amino acids was found to properly localize in the rhabdomeres, the light-sensing organelle of the photoreceptor cells. This constitutes a major difference to trafficking in vertebrates, which involves a conserved QVxPA motif at the very C-terminus. Further truncations of Rh1 indicated that proper localization requires the last amino acid residues of a region called helix 8 following directly the last transmembrane domain. Interestingly, the very C-terminus of invertebrate visual rhodopsins is extremely variable but helix 8 shows conserved amino acid residues that are not conserved in vertebrate homologs.
CONCLUSIONS/SIGNIFICANCE:
Despite impressive similarities in the folding and photoactivation of vertebrate and invertebrate visual rhodopsins, a striking difference exists between mammalian and fly rhodopsins in their requirements for proper targeting. Most importantly, the distal part of helix 8 plays a central role in invertebrates. Since the last amino acid residues of helix 8 are dispensable for rhodopsin folding and function, we propose that this domain participates in the recognition of targeting factors involved in transport to the rhabdomeres.
AuthorsInes Kock, Natalia A Bulgakova, Elisabeth Knust, Irmgard Sinning, Valérie Panneels
JournalPloS one (PLoS One) Vol. 4 Issue 7 Pg. e6101 (Jul 02 2009) ISSN: 1932-6203 [Electronic] United States
PMID19572012 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Rhodopsin
Topics
  • Amino Acid Sequence
  • Animals
  • Animals, Genetically Modified
  • Drosophila
  • Fluorescent Antibody Technique
  • Microscopy, Confocal
  • Molecular Sequence Data
  • Rhodopsin (chemistry, metabolism)
  • Sequence Homology, Amino Acid

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: