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A MICROARRAY TO ANALYZE METHYLATION PATTERNS OF E-CAD GENE 5'-CpG ISLANDS

机译:用于分析E-CAD基因5'-CpG岛甲基化模式的微阵列

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Aberrant methylation on the CpG sites in the promoter regions of the tumor suppressor gene has been shown to associate closely with carcinogenesis. Several studies suggest that the E-cadherin promoter frequently undergoes hypermethylation in multiform carcinogenesis. We have selected a 260 bp segment of a promoter of the E-cad gene as the target sequence and desighed a set of oligonucleotide probes to assemble a methylation specific oligonucleotide microarray to discriminate the methylation patterns of several adjacent CpG sites. We have established five calibration curves of the corresponding probes with fully methylated and unmethylated allele served as negative and positive target. And sequently this microarray assay has been simply applied for mapping methylation patterns in multiple CpG loci of E-cad gene in normal and acute leukemic samples. The methylation oligonucleotide microarray can be a useful and powerful tool to map methylation patterns in multiple CpG island sites.
机译:已经显示出肿瘤抑制基因的启动子区域中CpG位点上的异常甲基化,与致癌作用紧密相关。几项研究表明,E-Cadherin启动子经常在多种致癌物中经历高甲基化。我们选择了E-CAD基因的启动子作为靶序列的260bp段作为靶序列,并达到一组寡核苷酸探针,以组装甲基化特异性寡核苷酸微阵列以区分几个相邻的CpG位点的甲基化模式。我们已经建立了具有完全甲基化和未甲基化等位基因的相应探针的五种校准曲线,用作阴性和阳性靶标。并且序列地,这种微阵列测定仅用于在正常和急性白血病样品中映射e-CAD基因的多个CpG基因座中的甲基化模式。甲基化寡核苷酸微阵列可以是一种有用而强大的工具,用于在多个CpG岛地点映射甲基化图案。

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