Ho-Pun-Cheung Alexandre, Choblet Sylvie, Colineau Thomas, Abaibou Hafid, Zsoldos Daniela, Brengel-Pesce Karen, Grenier Jean, Cleuziat Philippe, Lopez-Crapez Evelyne
Cancer Research Center, Val d'Aurelle Cancer Institute, Montpellier, France.
Lab Invest. 2006 Mar;86(3):304-13. doi: 10.1038/labinvest.3700387.
With the increasing availability of genetic information and its relationship to human diseases, there is a growing need in the medical diagnostic field for technologies that can proceed to the parallel genotyping of multiple markers. In this paper, we report the development of a new flexible microarray-based method that aims to be inexpensive, accurate, and adapted to routine analysis. The construction of the MICAM (MICrosystem for Analysis in Medicine) DNA chip is based on the controlled electro-synthesis of a conducting polymer film bearing oligonucleotide probes on gold electrodes. First, accessible 3'OH-ends of grafted probes are directly used to conduct single template-dependent nucleotide extension reactions with fluorescence-labeled chain terminators. Then, the fluorescence of incorporated dideoxynucleotides on controls and probes of interest are recorded to assess base calling. Here, we present the development of the methodology to assign the genotype of TP53 (tumor protein p53) codon 72 polymorphism and its application to analysis of genomic DNA from cell lines and from human colorectal samples. The genotyping results obtained by mini-sequencing on the polypyrrole DNA chip were 100% concordant with data obtained by polymerase chain reaction-restriction fragment length polymorphism and direct sequencing. Moreover, the developed probe array assay has been successfully applied to the detection of TP53 loss of heterozygosity.
随着遗传信息的日益普及及其与人类疾病的关系,医学诊断领域对能够进行多个标记物平行基因分型的技术的需求日益增长。在本文中,我们报告了一种新的基于微阵列的灵活方法的开发,该方法旨在实现低成本、高精度并适用于常规分析。MICAM(医学分析微系统)DNA芯片的构建基于在金电极上对带有寡核苷酸探针的导电聚合物膜进行可控电合成。首先,接枝探针可及的3'OH末端直接用于与荧光标记的链终止剂进行单模板依赖性核苷酸延伸反应。然后,记录掺入的双脱氧核苷酸在对照和感兴趣探针上的荧光,以评估碱基识别。在此,我们展示了确定TP53(肿瘤蛋白p53)密码子72多态性基因型的方法的开发及其在细胞系和人类结肠直肠样本基因组DNA分析中的应用。通过在聚吡咯DNA芯片上进行微测序获得的基因分型结果与通过聚合酶链反应-限制性片段长度多态性和直接测序获得的数据100%一致。此外,所开发的探针阵列检测法已成功应用于TP53杂合性缺失的检测。