Fuchs Tania, Gavarini Sophie, Saunders-Pullman Rachel, Raymond Deborah, Ehrlich Michelle E, Bressman Susan B, Ozelius Laurie J
Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine, New York, New York 10029, USA.
Nat Genet. 2009 Mar;41(3):286-8. doi: 10.1038/ng.304. Epub 2009 Feb 1.
We report the discovery of a mutation in the THAP1 gene in three Amish-Mennonite families with mixed-onset primary torsion dystonia (also known as DYT6 dystonia). Another mutation in a German family with primary torsion dystonia suggests that THAP1 mutations also cause dystonia in other ancestry groups. We demonstrate that the missense mutation impairs DNA binding, suggesting that transcriptional dysregulation may contribute to the phenotype of DYT6 dystonia.
我们报告了在三个患有混合型原发性扭转性肌张力障碍(也称为DYT6肌张力障碍)的阿米什 - 门诺派家族中发现THAP1基因的一个突变。在一个患有原发性扭转性肌张力障碍的德国家族中的另一个突变表明,THAP1突变在其他血统群体中也会导致肌张力障碍。我们证明该错义突变损害了DNA结合,这表明转录失调可能导致DYT6肌张力障碍的表型。