Ge Xijin, Rubinstein Wendy S, Jung Yong-Chul, Wu Qingfa
Department of Mathematics and Statistics, South Dakota State University, Box 2220, Brookings, SD 57007, USA.
BMC Genomics. 2008 Jan 22;9:27. doi: 10.1186/1471-2164-9-27.
A large number of natural antisense transcripts have been identified in human and mouse genomes. Study of their potential functions clearly requires cost-efficient method for expression analysis.
Here we show that Affymetrix Exon arrays, which were designed to detect conventional transcripts in the sense orientation, can be used to monitor antisense expression across all exonic loci in mammalian genomes. Through modification of the cDNA synthesis protocol, we labeled single-strand cDNA in the reverse orientation as in the standard protocol, thus enabling the detection of antisense transcripts using the same array. Applying this technique to human Jurkat cells, we identified antisense transcription at 2,088 exonic loci of 1,516 UniGene clusters. Many of these antisense transcripts were not observed previously and some were validated by orientation-specific RT-PCR.
Our results suggest that with a modified protocol Affymetrix human, mouse and rat Exon arrays can be used as a routine method for genome-wide analysis of antisense transcription in these genomes.
在人类和小鼠基因组中已鉴定出大量天然反义转录本。对其潜在功能的研究显然需要经济高效的表达分析方法。
我们在此表明,旨在检测有义方向常规转录本的Affymetrix外显子阵列可用于监测哺乳动物基因组中所有外显子位点的反义表达。通过修改cDNA合成方案,我们像在标准方案中一样以相反方向标记单链cDNA,从而能够使用同一阵列检测反义转录本。将该技术应用于人类Jurkat细胞,我们在1516个单基因簇的2088个外显子位点鉴定出反义转录。其中许多反义转录本以前未被观察到,一些通过定向特异性RT-PCR得到验证。
我们的结果表明,通过修改方案,Affymetrix人类、小鼠和大鼠外显子阵列可作为这些基因组中反义转录全基因组分析的常规方法。