Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjects

Sci Rep. 2017 Dec 6;7(1):17105. doi: 10.1038/s41598-017-17361-7.

Abstract

The effect of Copy Number Variants (CNVs) on Type 2 Diabetes (T2D) remains little explored. The present study characterized large rare CNVs in 686 T2D and 194 non-T2D subjects of Mexican ancestry genotyped using the Affymetrix Genome-Wide Human SNP array 5.0. Rare CNVs with ≥ 100 kb length were identified using a stringent strategy based on merging CNVs calls generated using Birdsuit, iPattern and PennCNV algorithms. We applied three different strategies to evaluate the distribution of CNVs in the T2D and non-T2D samples: 1) Burden analysis, 2) Identification of CNVs in loci previously associated to T2D, and 3) Identification of CNVs observed only in the T2D group. In the CNV burden analysis, the T2D group showed a higher proportion of CNVs, and also a higher proportion of CNVs overlapping at least one gene than the non T2D group. Five of the six loci previously associated with T2D had duplications or deletions in the T2D sample, but not the non-T2D sample. A gene-set analysis including genes with CNVs observed only in the T2D group highlighted gene-sets related with sensory perception (olfactory receptors, OR) and phenylpyruvate tautomerase/dopachrome isomerase activity (MIF and DDT genes).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Algorithms
  • Case-Control Studies
  • DNA Copy Number Variations*
  • Diabetes Mellitus, Type 2 / genetics
  • Diabetes Mellitus, Type 2 / pathology*
  • Female
  • Gene Deletion
  • Gene Duplication
  • Genetic Loci
  • Genotype
  • Humans
  • Intramolecular Oxidoreductases / genetics
  • Kruppel-Like Transcription Factors / genetics
  • Male
  • Mexico
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Receptors, Odorant / genetics

Substances

  • Kruppel-Like Transcription Factors
  • Receptors, Odorant
  • ZNF74 protein, human
  • Intramolecular Oxidoreductases
  • dopachrome isomerase