Matsumura Hideo, Krüger Detlev H, Kahl Günter, Terauchi Ryohei
Iwate Biotechnology Research Center, Narita 22-174-4, Kitakami, Iwate, 024-0003, Japan.
Curr Pharm Biotechnol. 2008 Oct;9(5):368-74. doi: 10.2174/138920108785915157.
SuperSAGE is a variant of SAGE (Serial Analysis of Gene Expression) technology, which allows making transcript profiling by 26-bp tags extracted from cDNA employing the typeIII restriction enzyme EcoP15I. Its tag length is the longest among all the versions of SAGE, and is advantageous in tag-to-gene annotation, thereby allowing the technique to applicable to any eukaryotic life organisms. For model organisms with genome or cDNA sequences available, genes corresponding to 26-bp tags are uniquely defined by simple BLAST search. For non-model organisms without these sequence information, the 26-bp tag sequence is directly applicable to design PCR primer for amplifying cDNA of corresponding genes by 3'- or 5'-RACE. Furthermore, SuperSAGE allows various applications including "interaction transcriptome" and "SuperSAGE array". Emerging "Next Generation Sequencing" technologies perfectly complement SuperSAGE, and their combination has generated a novel transcriptome platform, that is superior to all the different microarray variants in terms of throughput, data quality and cost of analysis.
超级SAGE是基因表达系列分析(SAGE)技术的一种变体,它通过使用III型限制性内切酶EcoP15I从cDNA中提取的26bp标签进行转录本分析。其标签长度在所有SAGE版本中是最长的,在标签到基因的注释方面具有优势,从而使该技术适用于任何真核生物。对于有基因组或cDNA序列的模式生物,通过简单的BLAST搜索可以唯一确定与26bp标签对应的基因。对于没有这些序列信息的非模式生物,26bp标签序列可直接用于设计PCR引物,通过3'-或5'-RACE扩增相应基因的cDNA。此外,超级SAGE允许进行各种应用,包括“相互作用转录组”和“超级SAGE阵列”。新兴的“下一代测序”技术完美地补充了超级SAGE,它们的结合产生了一个新的转录组平台,在通量、数据质量和分析成本方面优于所有不同的微阵列变体。