From genotype to human β cell phenotype and beyond

Islets. 2012 Sep-Oct;4(5):323-32. doi: 10.4161/isl.22282. Epub 2012 Sep 1.

Abstract

Polygenic type 2 diabetes mellitus (T2DM) is a multi-factorial disease due to the interplay between genes and the environment. Over the years, several genes/loci have been associated with this type of diabetes, with the majority of them being related to β cell dysfunction. In this review, the available information on how polymorphisms in T2DM-associated genes/loci do directly affect the properties of human islet cells are presented and discussed, including some clinical implications and the role of epigenetic mechanisms.

Publication types

  • Review

MeSH terms

  • Cell Cycle Proteins / genetics
  • Diabetes Mellitus, Type 2 / genetics*
  • Epigenesis, Genetic
  • Genotype
  • Humans
  • Insulin-Secreting Cells / metabolism*
  • Phenotype
  • Polymorphism, Single Nucleotide
  • Protein Serine-Threonine Kinases / antagonists & inhibitors
  • Protein Serine-Threonine Kinases / genetics
  • Receptor, Melatonin, MT1 / genetics
  • Receptor, Melatonin, MT2
  • Repressor Proteins / genetics
  • Transcription Factor 7-Like 2 Protein / genetics

Substances

  • Cell Cycle Proteins
  • MTNR1B protein, human
  • Receptor, Melatonin, MT1
  • Receptor, Melatonin, MT2
  • Repressor Proteins
  • TCF7L2 protein, human
  • TRIB3 protein, human
  • Transcription Factor 7-Like 2 Protein
  • Protein Serine-Threonine Kinases