DYSBINDIN


'Dysbindin', short for 'dystrobrevin-binding protein 1', is a protein constituent of the dystrophin-associated protein complex of skeletal muscle cells. Dysbindin was discovered by the research group of Derek Blake via yeast two-hybrid screening for binding partners of α-dystrobrevin.[1] In addition, dysbindin is found in neural tissue of the brain, particularly in axon bundles and especially in certain axon terminals, notably mossy fiber synaptic terminals in the cerebellum and hippocampus.

Contents
Implications for Schizophrenia
References
External links

Implications for Schizophrenia


Much interest in dysbindin has arisen through pedigree-based family-association studies of families with a history of schizophrenia, where a strong association was found between expression of a particular dysbindin allele and a clinical expression of schizophrenia.[2] However, the exact link between dysbindin and schizophrenia remains highly controversial.

References


1. Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain, Benson et al, , , J Biol Chem, 2001
2. Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia, Straub et al, , , Am J Hum Genet, 2002

External links





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