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Silent SNPs: Impact on gene function and phenotype

Research output: Contribution to journalArticlepeer-review

229 Scopus citations

Abstract

Individuals carrying silent SNPs in the MDR1 gene encoding P-glycoprotein sometimes reveal altered P-glycoprotein pharmacokinetics. There is no rational explanation for why silent SNPs might have such effects, especially when no change in P-glycoprotein mRNA and protein expression levels has been observed. The purpose of this study was to perform careful ex vivo (in cells) analysis of the effects of the three polymorphisms (C1236T, G2677T C3435T) on P-glycoprotein expression and activity. As a result, it has been shown that silent polymorphisms (in particular, C3435T) in MDR1 can alter P-glycoprotein conformation and protein activity/substrate specificity. This study is of immense importance as it demonstrates for the first time that naturally occurring silent SNPs can lead to the synthesis of protein product with the same amino acid sequence but different structural and functional properties. Thus, silent SNPs should no longer be neglected in determining the likelihood of development of various diseases, and should be taken into account in personalized drug treatment and development programs. © 2007 Future Medicine Ltd.
Original languageEnglish
Pages (from-to)1075-1080
Number of pages6
JournalPharmacogenomics
Volume8
Issue number8
DOIs
StatePublished - Aug 1 2007

Keywords

  • Cotranslational protein folding
  • MDR1
  • P-glycoprotein
  • Personalized medicine
  • SNP
  • Silent substitution
  • Synonymous codon
  • Translation rates

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