x
Filter:
Filters applied
- Molecular Bases of Disease
- Baehr, WolfgangRemove Baehr, Wolfgang filter
- retinal degenerationRemove retinal degeneration filter
Molecular Bases of Disease
2 Results
- Molecular Bases of DiseaseOpen Access
The guanine nucleotide exchange factor Arf-like protein 13b is essential for assembly of the mouse photoreceptor transition zone and outer segment
Journal of Biological ChemistryVol. 292Issue 52p21442–21456Published online: October 31, 2017- Christin Hanke-Gogokhia
- Zhijian Wu
- Ali Sharif
- Hussein Yazigi
- Jeanne M. Frederick
- Wolfgang Baehr
Cited in Scopus: 21Arf-like protein 13b (ARL13b) is a small GTPase that functions as a guanosine nucleotide exchange factor (GEF) for ARL3-GDP. ARL13b is located exclusively in photoreceptor outer segments (OS) presumably anchored to discs by palmitoylation, whereas ARL3 is an inner segment cytoplasmic protein. Hypomorphic mutations affecting the ARL13b G-domain inactivate GEF activity and lead to Joubert syndrome (JS) in humans. However, the molecular mechanisms in ARL13b mutation–induced Joubert syndrome, particularly the function of primary cilia, are still incompletely understood. - NeurobiologyOpen Access
Arf-like Protein 3 (ARL3) Regulates Protein Trafficking and Ciliogenesis in Mouse Photoreceptors
Journal of Biological ChemistryVol. 291Issue 13p7142–7155Published online: January 25, 2016- Christin Hanke-Gogokhia
- Zhijian Wu
- Cecilia D. Gerstner
- Jeanne M. Frederick
- Houbin Zhang
- Wolfgang Baehr
Cited in Scopus: 71Arf-like protein 3 (ARL3) is a ubiquitous small GTPase expressed in ciliated cells of plants and animals. Germline deletion of Arl3 in mice causes multiorgan ciliopathy reminiscent of Bardet-Biedl or Joubert syndromes. As photoreceptors are elegantly compartmentalized and have cilia, we probed the function of ARL3 (ADP-ribosylation factor (Arf)-like 3 protein) by generating rod photoreceptor-specific (prefix rod) and retina-specific (prefix ret) Arl3 deletions. In predegenerate rodArl3−/− mice, lipidated phototransduction proteins showed trafficking deficiencies, consistent with the role of ARL3 as a cargo displacement factor for lipid-binding proteins.