Lee Myoyong, Xiang Charlie C, Trent Jeffrey M, Bittner Michael L
Cancer Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Anal Biochem. 2007 Sep 1;368(1):70-8. doi: 10.1016/j.ab.2007.05.010. Epub 2007 May 13.
Microarray fabrication using presynthesized long oligonucleotide is becoming increasingly important, but a study of large-scale array productions has not yet been published. We addressed the issue of fabricating oligonucleotide microarrays by spotting commercial presynthesized 65-mers with 5' amines representing 7500 murine genes. Amine-modified oligonucleotides were immobilized on glass slides having aldehyde groups via transient Schiff base formation followed by reduction to produce a covalent conjugate. When RNA derived from the same source was used for Cy3 and Cy5 labeling and hybridized to the same array, signal intensities spanning three orders of magnitude were observed and the coefficient of variance (CV) between the two channels for all spots was 8 to 10%. To ascertain the reproducibility of ratio determination of these arrays, two triplicate hybridizations (with fluorochrome reversal) comparing RNAs from a fibroblast (NIH3T3) and a breast cancer (JC) cell line were carried out. The 95% confidence interval for all spots in the six hybridizations was 0.60 to 1.66. This level of reproducibility allows use of the full range of pattern finding and discriminant analysis typically applied to complementary DNA (cDNA) microarrays. Further comparative testing was carried out with oligonucleotide microarrays, cDNA microarrays, and reverse transcription (RT)-PCR assays to examine the comparability of results across these different methodologies.
使用预合成的长寡核苷酸制造微阵列正变得越来越重要,但尚未有关于大规模阵列生产的研究发表。我们通过点样代表7500个小鼠基因的带有5'胺基的商业预合成65聚体来解决制造寡核苷酸微阵列的问题。胺修饰的寡核苷酸通过短暂的席夫碱形成固定在具有醛基的载玻片上,随后还原以产生共价共轭物。当使用来自同一来源的RNA进行Cy3和Cy5标记并与同一阵列杂交时,观察到信号强度跨越三个数量级,并且所有斑点的两个通道之间的变异系数(CV)为8%至10%。为了确定这些阵列比值测定的可重复性,进行了两次一式三份的杂交(荧光染料反转),比较来自成纤维细胞(NIH3T3)和乳腺癌(JC)细胞系的RNA。六次杂交中所有斑点的95%置信区间为0.60至1.66。这种可重复性水平允许使用通常应用于互补DNA(cDNA)微阵列的全套模式发现和判别分析。使用寡核苷酸微阵列、cDNA微阵列和逆转录(RT)-PCR分析进行了进一步的比较测试,以检查这些不同方法结果的可比性。