Systematic TOR1A non-c.907_909delGAG variant analysis in isolated dystonia and controls

Michael Zech, Angela Jochim, Sylvia Boesch, Sandrina Weber, Tobias Meindl, Annette Peters, Christian Gieger, Joerg Mueller, Michael Messner, Andres Ceballos-Baumann, Werner Poewe, Bernhard Haslinger, Juliane Winkelmann

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Background An increasing number of rare, functionally relevant non-c.907_909delGAG (non-ΔGAG) variants in TOR1A have been recognized, associated with phenotypic expressions different from classic DYT1 childhood-onset generalized dystonia. Only recently, DYT1 genotype-phenotype correlations have been proposed, awaiting further elucidation in independent cohorts. Methods We screened the entire coding sequence and the 5′-UTR region of TOR1A for rare non-ΔGAG sequence variants in a large series of 940 individuals with various forms of isolated dystonia as well as in 376 ancestry-matched controls. The frequency of rare, predicted deleterious non-ΔGAG TOR1A variants was assessed in the European sample of the Exome Aggregation Consortium (ExAC) dataset. Results In the case cohort, we identified a rare 5′-UTR variant (c.-39G > T), a rare splice-region variant (c.445-8T > C), as well as one novel (p.Ile231Asn) and two rare (p.Ala163Val, p.Thr321Met) missense variants, each in a single patient with adult-onset focal/segmental isolated dystonia. Of these variants, only p.Thr321Met qualified as possibly disease-related according to variant interpretation criteria. One novel, predicted deleterious missense substitution (p.Asn208Ser) was detected in the control cohort. Among European ExAC individuals, the carrier rate of rare, predicted deleterious non-ΔGAG variants was 0.4%. Conclusions Our study does not allow the establishment of genotype-specific clinical correlations for DYT1. Further large-scale genetic screening accompanied by comprehensive segregation and functional studies is required to conclusively define the contribution of TOR1A whole-gene variation to the pathogenesis of isolated dystonia.

Original languageEnglish
Pages (from-to)119-123
Number of pages5
JournalParkinsonism and Related Disorders
Volume31
DOIs
StatePublished - 1 Oct 2016
Externally publishedYes

Keywords

  • DYT1
  • Dystonia
  • Gene
  • Rare variant analysis
  • TOR1A

Fingerprint

Dive into the research topics of 'Systematic TOR1A non-c.907_909delGAG variant analysis in isolated dystonia and controls'. Together they form a unique fingerprint.

Cite this