Knight_2008_Hum.Mol.Genet_17_3847

Reference

Title : A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20 - Knight_2008_Hum.Mol.Genet_17_3847
Author(s) : Knight MA , Hernandez D , Diede SJ , Dauwerse HG , Rafferty I , van de Leemput J , Forrest SM , Gardner RJ , Storey E , van Ommen GJ , Tapscott SJ , Fischbeck KH , Singleton AB
Ref : Hum Mol Genet , 17 :3847 , 2008
Abstract :

Spinocerebellar ataxia type 20 (SCA20) has been linked to chromosome 11q12, but the underlying genetic defect has yet to be identified. We applied single-nucleotide polymorphism genotyping to detect structural alterations in the genomic DNA of patients with SCA20. We found a 260 kb duplication within the previously linked SCA20 region, which was confirmed by quantitative polymerase chain reaction and fiber fluorescence in situ hybridization, the latter also showing its direct orientation. The duplication spans 10 known and 2 unknown genes, and is present in all affected individuals in the single reported SCA20 pedigree. While the mechanism whereby this duplication may be pathogenic remains to be established, we speculate that the critical gene within the duplicated segment may be DAGLA, the product of which is normally present at the base of Purkinje cell dendritic spines and contributes to the modulation of parallel fiber-Purkinje cell synapses.

PubMedSearch : Knight_2008_Hum.Mol.Genet_17_3847
PubMedID: 18801880
Gene_locus related to this paper: human-DAGLA

Related information

Gene_locus human-DAGLA

Citations formats

Knight MA, Hernandez D, Diede SJ, Dauwerse HG, Rafferty I, van de Leemput J, Forrest SM, Gardner RJ, Storey E, van Ommen GJ, Tapscott SJ, Fischbeck KH, Singleton AB (2008)
A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20
Hum Mol Genet 17 :3847

Knight MA, Hernandez D, Diede SJ, Dauwerse HG, Rafferty I, van de Leemput J, Forrest SM, Gardner RJ, Storey E, van Ommen GJ, Tapscott SJ, Fischbeck KH, Singleton AB (2008)
Hum Mol Genet 17 :3847