Molecular dissection of the photoreceptor ribbon synapse: physical interaction of Bassoon and RIBEYE is essential for the assembly of the ribbon complex

• Published in: The Journal of cell biology 2005-02, Vol.168 (5), p.825-836
• Main Authors: tom Dieck, Susanne, Altrock, Wilko D, Kessels, Michael M, Qualmann, Britta, Regus, Hanna, Brauner, Dana, Fejtová, Anna, Bracko, Oliver, Gundelfinger, Eckart D, Brandstätter, Johann H
• Format: Article
• Language: English
• Subjects: Animals; Antibodies; Antiserum; Cell membranes; Cellular biology; DNA-Binding Proteins - metabolism; Fluorescent Antibody Technique; Immunohistochemistry; Mice; Nerve Tissue Proteins - metabolism; Nervous system; Neurons; Phenotypes; Phosphoproteins - metabolism; Photoreceptor Cells - metabolism; Photoreceptors; Proteins; Retina; Ribbons; Synapses; Synapses - metabolism; Yeasts
• ISSN: 0021-9525; 1540-8140
• DOI: 10.1083/jcb.200408157

The ribbon complex of retinal photoreceptor synapses represents a specialization of the cytomatrix at the active zone (CAZ) present at conventional synapses. In mice deficient for the CAZ protein Bassoon, ribbons are not anchored to the presynaptic membrane but float freely in the cytoplasm. Exploiting this phenotype, we dissected the molecular structure of the photoreceptor ribbon complex. Identifiable CAZ proteins segregate into two compartments at the ribbon: a ribbon-associated compartment including Piccolo, RIBEYE, CtBP1/BARS, RIM1, and the motor protein KIF3A, and an active zone compartment including RIM2, Munc13-1, a Ca²⁺ channel [alpha]1 subunit, and ERC2/CAST1. A direct interaction between the ribbon-specific protein RIBEYE and Bassoon seems to link the two compartments and is responsible for the physical integrity of the photoreceptor ribbon complex. Finally, we found the RIBEYE homologue CtBP1 at ribbon and conventional synapses, suggesting a novel role for the CtBP/BARS family in the molecular assembly and function of central nervous system synapses.