Iwate Biotechnology Research Center, Kitakami, Japan.
PLoS One. 2010 Aug 6;5(8):e12010. doi: 10.1371/journal.pone.0012010.
We established a protocol of the SuperSAGE technology combined with next-generation sequencing, coined "High-Throughput (HT-) SuperSAGE". SuperSAGE is a method of digital gene expression profiling that allows isolation of 26-bp tag fragments from expressed transcripts. In the present protocol, index (barcode) sequences are employed to discriminate tags from different samples. Such barcodes allow researchers to analyze digital tags from transcriptomes of many samples in a single sequencing run by simply pooling the libraries. Here, we demonstrated that HT-SuperSAGE provided highly sensitive, reproducible and accurate digital gene expression data. By increasing throughput for analysis in HT-SuperSAGE, various applications are foreseen and several examples are provided in the present study, including analyses of laser-microdissected cells, biological replicates and tag extraction using different anchoring enzymes.
我们建立了一个结合下一代测序的 SuperSAGE 技术方案,称为“高通量(HT-)SuperSAGE”。SuperSAGE 是一种数字基因表达谱分析方法,可从表达的转录本中分离出 26 个碱基对的标签片段。在本方案中,索引(条形码)序列用于区分来自不同样本的标签。通过这种条形码,研究人员可以通过简单地将文库混合,在单个测序运行中分析来自许多样本转录组的数字标签。在这里,我们证明了 HT-SuperSAGE 提供了高度敏感、可重复和准确的数字基因表达数据。通过增加 HT-SuperSAGE 分析的通量,预计会有各种应用,本研究提供了几个示例,包括激光显微切割细胞、生物重复和使用不同锚定酶进行标签提取的分析。