Single nucleotide polymorphism characterization by mRNA expression imbalance assessment.

Leszek Wojnowski, Jürgen Brockmöller
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引用次数: 17

Abstract

The functional characterization of single nucleotide polymorphism (SNPs) represents a major challenge for pharmacogenetics and related research areas. Here, we propose a procedure, termed mRNA expression imbalance assessment, that can be applied to detect cis-acting SNPs with an effect on mRNA expression. The procedure is based on the observation that the relative transcript levels derived from the two alleles of an autosomal gene are reflected in the sequence of the amplified cDNA. The key element of the procedure is the detection of a discrepancy between the specific nucleotide signal intensity of a marker SNP in the genomic DNA and in the cDNA. We used the CYP3A5*1/*3 polymorphism as a proof principle for this approach. In this case, we could even demonstrate that the procedure works equally well with the appropriate tissue samples and in silico, using the existing databanks of sequences. In conclusion, the procedure provides a fast and easy tool, which may facilitate identification of functional SNPs.

通过mRNA表达不平衡评估来鉴定单核苷酸多态性。
单核苷酸多态性(snp)的功能表征是药物遗传学和相关研究领域的一个重大挑战。在这里,我们提出了一个程序,称为mRNA表达不平衡评估,可用于检测顺式作用的snp与mRNA表达的影响。该程序是基于观察到来自常染色体基因的两个等位基因的相对转录水平反映在扩增的cDNA序列中。该程序的关键要素是检测基因组DNA和cDNA中标记SNP的特定核苷酸信号强度之间的差异。我们使用CYP3A5*1/*3多态性作为该方法的证明原理。在这种情况下,我们甚至可以证明,使用现有的序列数据库,该程序在适当的组织样本和计算机上同样有效。总之,该方法提供了一种快速简便的工具,可以方便地识别功能性snp。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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