Assessment of the association between NUS1 variants and essential tremor

Neurosci Lett. 2021 Jan 1:740:135441. doi: 10.1016/j.neulet.2020.135441. Epub 2020 Oct 24.

Abstract

Background: A recent study on early onset Parkinson's disease (PD) revealed that NUS1 is a risk gene for PD. Clinically, essential tremor (ET) is closely related to PD. In this study, we aimed to detect NUS1 variants and assess the effect of those variants on patients with ET.

Methods: The 5 coding regions and the exon-intron boundaries of NUS1 were directly sequenced in 395 patients with ET and an equal number of healthy controls, matched for age and sex. The function of variants was assessed by pathogenic predictive software programs. Genetic analysis of variants was used to evaluate susceptibility to ET.

Results: A total of 6 exonic variants were identified, including 3 synonymous and 3 missense variants. The non-synonymous variants were predicted to be tolerable. No variants had significant association with ET (none of the p-values were less than 0.05, using Fisher's exact test).

Conclusion: Our study suggested that NUS1 variants may not contribute to the risk of ET.

Keywords: Essential tremor; NUS1variants; association study; mutation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Asian People
  • Case-Control Studies
  • China / epidemiology
  • Essential Tremor / epidemiology
  • Essential Tremor / genetics*
  • Exons / genetics
  • Female
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Variation
  • High-Throughput Screening Assays
  • Humans
  • Introns / genetics
  • Male
  • Mass Screening
  • Middle Aged
  • Mutation, Missense / genetics
  • Receptors, Cell Surface / genetics*
  • Software

Substances

  • NUS1 protein, human
  • Receptors, Cell Surface