Rondeau Gaëlle, McClelland Michael, Nguyen Toan, Risques Rosana, Wang Yipeng, Judex Martin, Cho Ann H, Welsh John
Sidney Kimmel Cancer Center 10835 Altman Row, San Diego, CA 92121, USA.
Nucleic Acids Res. 2005 Jun 24;33(11):e100. doi: 10.1093/nar/gni095.
Low abundance mRNAs are more difficult to examine using microarrays than high abundance mRNAs due to the effect of concentration on hybridization kinetics and signal-to-noise ratios. This report describes the use of low complexity representations (LCRs) of mRNA as the targets for cDNA microarrays. Individual sequences in LCRs are more highly represented than in the mRNA populations from which they are derived, leading to favorable hybridization kinetics. LCR targets permit the measurement of abundance changes that are difficult to measure using oligo(dT) priming for target synthesis. An oligo(dT)-primed target and three LCRs detect twice as many differentially regulated genes as could be detected by the oligo(dT)-primed target alone, in an experiment in which serum-starved fibroblasts responded to the reintroduction of serum. Thus, this target preparation strategy considerably increases the sensitivity of cDNA microarrays.
由于浓度对杂交动力学和信噪比的影响,与高丰度mRNA相比,使用微阵列检测低丰度mRNA更加困难。本报告描述了使用mRNA的低复杂度代表序列(LCR)作为cDNA微阵列的靶标。LCR中的单个序列比其来源的mRNA群体中具有更高的代表性,从而产生良好的杂交动力学。LCR靶标能够测量使用oligo(dT)引物进行靶标合成时难以测量的丰度变化。在血清饥饿的成纤维细胞对血清重新引入作出反应的实验中,一个oligo(dT)引物靶标和三个LCR检测到的差异调节基因数量是单独使用oligo(dT)引物靶标所能检测到的两倍。因此,这种靶标制备策略显著提高了cDNA微阵列的灵敏度。