Silent SNPs: impact on gene function and phenotype

被引:212
作者
Komar, Anton A. [1 ]
机构
[1] Cleveland State Univ, Dept Biol Geol & Environm Sci, Cleveland, OH 44115 USA
关键词
cotranslational protein folding; MDR1; personalized medicine; P-glycoprotein; silent substitution; SNP; synonymous codon; translation rates;
D O I
10.2217/14622416.8.8.1075
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:1075 / 1080
页数:6
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