Machl Andreas W, Schaab Christoph, Ivanov Igor
GPC Biotech AG, Fraunhoferstrasse 20, D-82152, Planegg/Martinsried, Germany.
Nucleic Acids Res. 2002 Nov 15;30(22):e127. doi: 10.1093/nar/gnf127.
Gene expression studies using cDNA arrays require robust and sensitive detection methods. Being extremely sensitive, radioactive detection suffers from the influence of signals positioned in each other's vicinity, the 'neighbourhood' effect. This limits the gene density of arrays and the quality of the results obtained. We have investigated the quantitative influence of different parameters on the 'neighbourhood' effect. By using a model experimental system, we could show that the effect is linear and depends only on the intensity of the hybridisation signal. We identified a common factor that can describe the influence of the neighbour spots based on their intensities. This factor is <1%, but it has to be taken into account if a high dynamic range of gene expression is to be detected. We could also derive the factor, although with less precision, from comparison of duplicate spots on arrays of 4565 different clones and replication of the hybridisation experiments. The calculated coefficient applied to our actual experimental results not only revealed previously undetected tissue or cell-specific expression differences, but also increased the dynamic range of detection. It thus provides a relatively simple way of improving DNA array data quality with few experimental modifications.
使用cDNA阵列进行基因表达研究需要强大且灵敏的检测方法。放射性检测极为灵敏,但会受到彼此相邻信号的影响,即“邻域”效应。这限制了阵列的基因密度以及所得结果的质量。我们研究了不同参数对“邻域”效应的定量影响。通过使用一个模型实验系统,我们能够表明该效应是线性的,并且仅取决于杂交信号的强度。我们确定了一个共同因子,该因子可根据相邻斑点的强度描述其影响。这个因子小于1%,但如果要检测基因表达的高动态范围,就必须将其考虑在内。我们还可以通过比较4565个不同克隆阵列上的重复斑点以及杂交实验的重复来得出该因子,尽管精度较低。应用于我们实际实验结果的计算系数不仅揭示了先前未检测到的组织或细胞特异性表达差异,还增加了检测的动态范围。因此,它提供了一种通过很少的实验修改来提高DNA阵列数据质量的相对简单方法。