No association of the SUMO4 polymorphism M55V variant in type 2 diabetes in Iranian subjects

Diabetes Res Clin Pract. 2010 Nov;90(2):191-5. doi: 10.1016/j.diabres.2010.05.033. Epub 2010 Aug 21.

Abstract

Introduction: Diabetes mellitus incidence has an increasing rate and it's genetic aspect is an important approach as a risk factor and predictive value in this disorder. In some population, SUMO4, a regulator of NF-κB, gene polymorphism is associated with diabetes. A single-nucleotide polymorphism was detected in SUMO4; substituting a highly conserved methionine with a valine residue (M55V). We studied the association between M55V polymorphism in the SUMO4 gene insusceptibility of type 2 diabetes in patients with type 2 diabetes.

Materials and methods: Participants were 50 patients with type 2 diabetes and 50 control Iranian subjects. Genotyping was done using polymorphism chain reaction (PCR) technique and subsequent cleavage by restriction endonuclease (RFLP) for the M55V SUMO4 gene variant.

Results: The frequency of SUMO4 AA, AG and GG were 13%, 25% and 12% in control group and 20%, 22%, 18% in the type 2 diabetes patients respectively. The SUMO4 M55V variant was not associated with the susceptibility of type 2 diabetes.

Conclusion: The study indicates that the SUMO4 gene M55V variant was not associated with the susceptibility of the type 2 diabetes polymorphism.

MeSH terms

  • Adult
  • Amino Acid Substitution
  • Diabetes Mellitus, Type 2 / genetics*
  • Female
  • Gene Frequency
  • Humans
  • Incidence
  • Iran / epidemiology
  • Male
  • Middle Aged
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Polymorphism, Single Nucleotide*
  • Reference Values
  • Small Ubiquitin-Related Modifier Proteins / genetics*

Substances

  • SUMO4 protein, human
  • Small Ubiquitin-Related Modifier Proteins