Glutathione S-transferase copy number variation alters lung gene expression. Academic Article uri icon

Overview

MeSH

  • Adult
  • Alleles
  • Female
  • Gene Expression Profiling
  • Genotype
  • Homozygote
  • Humans
  • Male
  • Middle Aged
  • Oligonucleotide Array Sequence Analysis
  • Polymorphism, Genetic

MeSH Major

  • Gene Dosage
  • Gene Expression Regulation
  • Glutathione Transferase
  • Lung

abstract

  • The glutathione S-transferase (GST) enzymes catalyse the conjugation of xenobiotics to glutathione. Based on reports that inherited copy number variations (CNVs) modulate some GST gene expression levels, and that the small airway epithelium (SAE) and alveolar macrophages (AMs) are involved early in the pathogenesis of smoking-induced lung disease, we asked: do germline CNVs modulate GST expression levels in SAE and AMs? Microarrays were used to survey GST gene expression and determine CNVs genotypes in SAE and AMs obtained by bronchoscopy from current smokers and nonsmokers. 26% of subjects were null for both GSTM1 alleles, with reduced GSTM1 mRNA levels seen in both SAE and AMs. 30% of subjects had homozygous deletions of GSTT1, with reduced mRNA levels in both tissues. Interestingly, GSTT2B exhibited homozygous deletion in the blood of 27% of subjects and was not expressed in SAE in the remainder of subjects, but was expressed in AMs of heterozygotes and wild-type subjects, proportionate to genotype. These data show a germline CNV-mediated linear relationship of genotype with expression level, suggesting minimal compensation of gene expression levels in heterozygotes, consistent with GST polymorphisms playing a role in the risk of smoking-associated, xenobiotic-induced lung disease.

publication date

  • July 2011

has subject area

  • Adult
  • Alleles
  • Female
  • Gene Dosage
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Genotype
  • Glutathione Transferase
  • Homozygote
  • Humans
  • Lung
  • Male
  • Middle Aged
  • Oligonucleotide Array Sequence Analysis
  • Polymorphism, Genetic

Research

keywords

  • Journal Article

Identity

Language

  • eng

PubMed Central ID

  • PMC3399270

Digital Object Identifier (DOI)

  • 10.1183/09031936.00029210

PubMed ID

  • 21349909

Additional Document Info

start page

  • 15

end page

  • 28

volume

  • 38

number

  • 1