Korn Kerstin, Gardellin Paola, Liao Bohao, Amacker Mario, Bergström Asa, Björkman Henrik, Camacho Agnès, Dörhöfer Sabine, Dörre Klaus, Enström Johanna, Ericson Thomas, Favez Tatiana, Gösch Michael, Honegger Adrian, Jaccoud Sandra, Lapczyna Markus, Litborn Erik, Thyberg Per, Winter Holger, Rigler Rudolf
Gnothis AB, Electrum 212, SE-164 40 Kista, Sweden.
Nucleic Acids Res. 2003 Aug 15;31(16):e89. doi: 10.1093/nar/gng089.
Recent developments of single molecule detection techniques and in particular the introduction of fluorescence correlation spectroscopy (FCS) led to a number of important applications in biological research. We present a unique approach for the gene expression analysis using dual-color cross-correlation. The expression assay is based on gene-specific hybridization of two dye-labeled DNA probes to a selected target gene. The counting of the dual-labeled molecules within the solution allows the quantification of the expressed gene copies in absolute numbers. As detection and analysis by FCS can be performed at the level of single molecules, there is no need for any type of amplification. We describe the gene expression assay and present data demonstrating the capacity of this novel technology. In order to prove the gene specificity, we performed experiments with gene-depleted total cDNA. The biological application was demonstrated by quantifying selected high, medium and low abundant genes in cDNA prepared from HL-60 cells.
单分子检测技术的最新进展,尤其是荧光相关光谱法(FCS)的引入,催生了生物研究中的许多重要应用。我们提出了一种使用双色互相关进行基因表达分析的独特方法。该表达测定基于两个染料标记的DNA探针与选定靶基因的基因特异性杂交。溶液中双标记分子的计数允许以绝对数量对表达的基因拷贝进行定量。由于FCS的检测和分析可以在单分子水平上进行,因此无需任何类型的扩增。我们描述了基因表达测定,并展示了证明这项新技术能力的数据。为了证明基因特异性,我们用基因缺失的总cDNA进行了实验。通过对从HL-60细胞制备的cDNA中选定的高、中、低丰度基因进行定量,证明了其生物学应用。