Usage of mitochondrial D-loop variation to predict risk for Huntington disease

Abstract

Huntington’s disease (HD) is an inherited autosomal neurodegenerative disease caused by the abnormal expansion of the CAG repeats in the Huntingtin (Htt) gene. It has been proven that mitochondrial dysfunction is contributed to the pathogenesis of Huntington’s disease. The mitochondrial displacement loop (D-loop) is proven to accumulate mutations at a higher rate than other regions of mtDNA. Thus, we hypothesized that specific SNPs in the D-loop may contribute to the pathogenesis of Huntington’s disease. In the present study, 30 patients with Huntington’s disease and 463 healthy controls were evaluated for mitochondrial mutation sites within the D-loop region using PCR-sequencing method. Sequence analysis revealed 35 variations in HD group from Cambridge Mitochondrial Sequences. A significant difference (p < 0.05) was seen between patients and control group in eight SNPs. Polymorphisms at C16069T, T16126C, T16189C, T16519C and C16223T were correlated with an increased risk of HD while SNPs at C16150T, T16086C and T16195C were associated with a decreased risk of Huntington’s disease.

• Displacement loop
• Huntington’s disease
• mitochondrial DNA
• PCR-sequencing method
• single nucleotide polymorphism

Declaration of interest

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article. This research was supported by a research grant from Iran University of Medical Sciences.