Genetic variants in multisynthetase complex genes are associated with DNA damage levels in Chinese populations

Mutat Res. 2016 Apr:786:8-13. doi: 10.1016/j.mrfmmm.2016.01.006. Epub 2016 Jan 25.

Abstract

Aminoacyl-tRNA synthetases (ARSs) and ARS-interacting multi-functional proteins (AIMPs) form a multisynthetase complex (MSC) and play an important role in the process of DNA damage repair. We hypothesized that genetic variants in key ARSs and AIMPs might regulate the DNA damage response. Therefore, we systematically screened 23 potentially functional polymorphisms in MSC genes and evaluated the association between the genetic variants and DNA damage levels in 307 subjects from three cities in southern, central and northern China (Zhuhai, Wuhan and Tianjin, respectively). We examined personal 24-h PM2.5 exposure levels and DNA damage levels in peripheral blood lymphocytes for each subject. We found that the variant allele of rs12199241 in AIMP3 was significantly associated with DNA damage levels (β=0.343, 95%CI: 0.133-0.554, P=0.001). Meanwhile, the results of rs5030754 in EPRS and rs3784929 in KARS indicated their suggestive roles in DNA damage processes (β=0.331, 95%CI: 0.062-0.599, P=0.016 for rs5030754; β=0.192, 95%CI: 0.016-0.368, P=0.033 for rs3784929, respectively). After multiple testing, rs12199241 was still significantly associated with DNA damage levels. Combined analysis of these three polymorphisms showed a significant allele-dosage association between the number of risk alleles and higher DNA damage levels (Ptrend<0.001). These findings indicate that genetic variants in MSC genes may account for PM2.5-modulated DNA damage levels in Chinese populations.

Keywords: DNA damage; Genetic variants; MSC genes; PM(2.5).

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Amino Acyl-tRNA Synthetases / genetics*
  • Asian People / genetics*
  • China
  • Comet Assay
  • DNA Damage*
  • DNA Repair
  • Databases, Genetic
  • Gene Frequency
  • Genetic Variation*
  • Genotyping Techniques
  • Humans
  • Lymphocytes / metabolism
  • Lysine-tRNA Ligase / genetics
  • Peptide Elongation Factors / genetics
  • Polymorphism, Single Nucleotide
  • Tumor Suppressor Proteins / genetics

Substances

  • EEF1E1 protein, human
  • Peptide Elongation Factors
  • Tumor Suppressor Proteins
  • Amino Acyl-tRNA Synthetases
  • glutamyl-prolyl-tRNA synthetase
  • Lysine-tRNA Ligase