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药物基因组学:利用氨基酸特性分析CYP2D6基因中的单核苷酸多态性

Pharmacogenomics: analysing SNPs in the CYP2D6 gene using amino acid properties.

作者信息

Ebbert Mark T W, Beckstead Wesley A, O'Connor Timothy D, Clement Mark J, McClellan David A

机构信息

Department of Integrative Biology and Computer Science, Brigham Young University, 3370 TMCB, Provo, Utah 84602, USA.

出版信息

Int J Bioinform Res Appl. 2007;3(4):471-9. doi: 10.1504/IJBRA.2007.015415.

Abstract

The CYP2D6 gene is responsible for metabolising a large portion of the commonly prescribed drugs. Because of its importance, various approaches have been taken to analyse CYP2D6 and Single Nucleotide Polymorphisms (SNPs) throughout its sequence. This study introduces a novel method to analyse the effects of SNPs on encoded protein complexes by focusing on the biochemical properties of each non-synonymous substitution using the program TreeSAAP. Our results show four SNPs in CYP2D6 that exhibit radical changes in amino acid properties which may cause a lack of functionality in the CYP2D6 gene and contribute to a person's inability to metabolise specific drugs.

摘要

细胞色素P450 2D6(CYP2D6)基因负责代谢大部分常用处方药。因其重要性,人们采用了各种方法来分析CYP2D6及其整个序列中的单核苷酸多态性(SNP)。本研究引入了一种新方法,通过使用TreeSAAP程序关注每个非同义替换的生化特性,来分析SNP对编码蛋白复合物的影响。我们的结果显示,CYP2D6中有四个SNP表现出氨基酸特性的显著变化,这可能导致CYP2D6基因功能缺失,并导致个体无法代谢特定药物。

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