Behrensdorf Heike A, Pignot Marc, Windhab Norbert, Kappel Andreas
Nanogen Recognomics GmbH, Industriepark Hoechst, Building G830, 65926 Frankfurt am Main, Germany.
Nucleic Acids Res. 2002 Jul 15;30(14):e64. doi: 10.1093/nar/gnf063.
We have developed a method for the de novo discovery of genetic variations, including single nucleotide polymorphisms and mutations, on microelectronic chip devices. The method combines the features of electronically controlled DNA hybridisation on open-format microarrays, with mutation detection by a fluorescence-labelled mismatch- binding protein. Electronic addressing of DNA strands to distinct test sites of the chip allows parallel analysis of several individuals, as demonstrated for mutations in different exons of the p53 gene. This microelectronic chip-based mutation discovery assay may substitute for time-consuming sequencing studies and will complement existing technologies in genomic research.
我们已经开发出一种在微电子芯片设备上从头发现遗传变异(包括单核苷酸多态性和突变)的方法。该方法将开放式微阵列上电子控制的DNA杂交特性与荧光标记的错配结合蛋白进行突变检测相结合。将DNA链电子寻址到芯片的不同测试位点可对多个个体进行平行分析,如对p53基因不同外显子中的突变所做的演示。这种基于微电子芯片的突变发现检测方法可能会替代耗时的测序研究,并将补充基因组研究中的现有技术。